LIST OF PUBLICATIONS
[176]
Complexity-Building Exhaustive Dearomatization of Benzenoid Aromatics within an ESIPT-Initiated Three-Step Photochemical Cascade. Beduru, S.; Huple, D.B.; Kutateladze, A.G. Angew. Chem. Int. Ed. , 2024, e202415176. [DOI: 10.1002/anie.202415176]
[175]
Oxidative Control of Photoinduced Cascade Electrocyclizations in Aromatic Azido Imines to Access Complex Fused Imidazoles or Pyrazoles. Reddy, D.S.; Novitskiy, I.M.; Beloglazkina, A.A.; Kutateladze A.G. Org. Lett., 2024, 26, 2558. [DOI: 10.1021/acs.orglett.4c00361]
[174]
Reassignment of the Structure of Setosol. Bates, R.W.; Elyashberg, M.; Kutateladze, A.G.; Williams, C.M. Eur. J. Org. Chem., 2024, e202400431. [DOI: 10.1002/ejoc.202400431]
[173]
Systematic Photoassisted Access to Designer Polyheterocycles via Modular Blocks and Scaffolding. Holt. T. A.; Novitskiy, I. M.; Kutateladze, A. G. Org. Lett., 2024, 26, (3), 734-738. [DOI: 10.1021/acs.orglett.3c04186]
[172]
Kallopterolides A–I, a New Subclass of seco-Diterpenes Isolated from the Southwestern Caribbean Sea Plume Antillogorgia kallos. Marrero, J.; Amador, L.A.; Novitskiy, I.M.; Kutateladze, A.G.; Rodriguiez, A.D. Molecules, 2024, 29, 2493. [DOI: 10.3390/molecules29112493]
[171]
Complexity-Building Photoinduced Cascade Involving Csp2-Csp3 Coupling of Aromatic Amides via [2 + 2] Reactivity of ESIPT Generated o-Azaxylylenes. Reddy, D.S.; Novitskiy, I.M.; Kutateladze, A.G. Org. Lett., 2023, 25, 1131-1135. [DOI: 10.1021/acs.orglett.3c00092]
[170]
Complexity-Building ESIPT-Assisted Synthesis of Fused Polyheterocyclic Sulfonamides. Beduru, S.; Kutateladze, A. G. Molecules, 2023, 28, 6549. [DOI: 10.3390/molecules28186549]
[169]
seco-Pregnane Glycosides from Australian Caustic Vine (Cynanchum viminale subsp. australe) Xue. Y.; Savchenko A.I.; Agnew-Francis, K.A.; Miles, J.A.; Holt, T.; Lu, H.; Chow, S.; Forster, P.I.; Boyle, G. M.; Ross, B.P.; Fisher, K.; Kutateladze, A.G.; Williams, C.M. J. Nat. Prod. , 2023, 86, 490-497. [DOI: 10.1021/acs.jnatprod.2c01037]
[168]
Arneroma B: Structure reassignment and total synthesis. Deepak, N.M.S.; Kutateladze, A.G.; Elyashberg, M.; Williams, C.M.; Bates, R.W. Tetrahedron, 2023, 147, 133670. [DOI: 10.1016/j.tet.2023.133670]
[167]
Structural Reassignment of Two Polyenol Natural Products. Kutateladze, A.G.; Bates, R.W.; Elyashberg, M.; Williams C.M. Eur. J. Org. Chem., 2023, e202201316. [DOI: 10.1002/ejoc.202201316]
[166]
Reassignmentof the Structureof Janthinolide A. Bates, R.W.; Elyashberg, M.; Kutateladze, A.G.; Williams, C.M. Eur. J. Org. Chem., 2023, 26, e202300910. [DOI: https://doi.org/10.1002/ejoc.202300910]
[165]
Rearrangements of the Radical Cations of 3-Aryl-5-fluoroisoxazoles: Further Evidence for Existence of Benzocyclopropenyl Cation. Bondarenko, O.B.; Komarov, A.I.; Nikolaeva, S.N.; Holt, T.A.; Kutateladze, A.G.; Gloriozov, I.P. J. Am. Soc. Mass Spectrom., 2023, 34, 2547-2555. [DOI: 10.1021/jasms.3c00267]
[164]
Penicitone: Structural Reassignment of a Proposed Natural Product Acid Chloride. Novitskiy, I.M.; Elyashberg, M.; Bates, R.W.; Kutateladze, A.G.; Williams, C.M. Org. Lett., 2023, 25, 7796-7799. [DOI: 10.1021/acs.orglett.3c02859]
[163]
Brief overview of recently reported misassigned natural products and their in silico revisions enabled by DU8ML, a machine learning-augmented DFT computational NMR method. Novitskiy, I.M.; Kutateladze, A.G. Nat. Prod. Rep., 2022, 39, 2003-2007. [DOI: 10.1039/D2NP00051B]
[162]
Maximizing Step-Normalized Increases in Molecular Complexity: Formal [4+2+2+2] Photoinduced Cyclization Cascade to Access Polyheterocycles Possessing Privileged Substructures. Reddy, D.S.; Novitskiy, I.M.; Kutateladze, A.G. Angew. Chem. Int. Ed., 2022, 61, (4), e202112573. [DOI: 10.1002/anie.202112573] Angewandte's Hot Paper
[161]
Peculiar Reaction Products and Mechanisms Revisited with Machine Learning-Augmented Computational NMR. Novitskiy, I.M.; Kutateladze, A.G. J. Org. Chem., 2022, 87, (13), 8589-8598. [DOI: 10.1021/acs.joc.2c00749] ACS Editors' Choice
[160]
DU8ML: Machine Learning-Augmented Density Functional Theory Nuclear Magnetic Resonance Computations for High-Throughput In Silico Solution Structure Validation and Revision of Complex Alkaloids. Novitskiy, I.M.; Kutateladze, A.G. J. Org. Chem., 2022, 87, (7), 4818-4828. [DOI: 10.1021/acs.joc.2c00169]
[159]
Reassignment of Improbable Natural Products Identified through Chemical Principle Screening. Elyashberg, M.; Novitskiy, I. M.; Bates, R. W.; Kutateladze, A. G.; Williams, C. M. Eur. J. Org. Chem., 2022, 2022, (34), e202200572. [DOI: 10.1002/ejoc.202200572] (Very Important Paper)
[158]
DU8+ Computations Reveal a Common Challenge in the Structure Assignment of Natural Products Containing a Carboxylic Anhydride Moiety. Novitskiy, I.M.; Kutateladze, A.G. J. Org. Chem., 2021, 86, 17511-17515. [DOI: 10.1021/acs.joc.1c02291]
[157]
Structure revision of ent-kaurane diterpenoids, isoserrins A, B, and D, enabled by DU8+ computation of their NMR spectral data. Novitskiy, I.M.; Holt, T.A.; Kutateladze, A.G. Mendeleev Comm. , 2021, 31, 300-301. [DOI: 10.1016/j.mencom.2021.05.007]
[156]
The Discreet Structural Diversity of Briarellins: DU8+ Guided Multiple Structure Revisions Yielded Two Unknown Structural Types. Holt, T. A.; Reddy, D. S.; Huple, D. B.; West, L. M.; Rodriguez, A. D.; Crimmins, M. T.; Kutateladze, A. G. J. Org. Chem., 2020, 85, (9), 6201-6205. [DOI: 10.1021/acs.joc.0c00555]
[155]
EBC-232 and 323:A Structural Conundrum Necessitating Unification of Five In Silico Prediction and Elucidation Methods. Maslovskaya, L. A.; Savchenk, A. I.; Krenske, E. H.; Chow, S.; Holt, T.; Gordon, V. A.; Reddell, P. W.; Pierce, C. J.; Parsons, P. G.; Boyle, G. M.; Kutateladze, A. G.; Williams, C. M. Chem. Eur. J., 2020, 26, 11862-11867. [DOI: 10.1002/chem.202001884]
[154]
Stereochemical revision of xylogranatin F by GIAO and DU8+ NMR calculations. Liu, Y.; Holt, T. A.; Kutateladze, A. G.; Newhouse, T. R. Chirality, 2020, 32, 515-523. [DOI: 10.1002/chir.23189]
[153]
Dichotomy in the reactivity of 2-methyltetrahydroquinazoline 1-oxides towards aldehydes: An unprecedented condensation with simultaneous reduction of the N-oxide fragment. Sedenkova, K. N.;Terekhin, A. V.; Abdrashitova, I. V.; Vasilenko, D. A.; Sadovnikov, K. S.; Gracheva, Y. A.; Grishin, Y. K.; Holt, T. A.; Kutateladze, A. G.; Kuznetsova, T. S.; Milaeva, E. R.; Averina, E. B. Tetrahedron Lett., 2020, 61, (11), 151605. [DOI: 10.1016/j.tetlet.2020.151605]
[152]
Photoinitiated Cascade for Rapid Access to Pyrroloquinazolinone Core of Vasicinone, Luotonins, and Related Alkaloids. Reddy, D. S.; Kutateladze, A. G. Org. Lett., 2019, 21, (8), 2855-2858.. [DOI: 10.1021/acs.orglett.9b00858]
[151]
Natural Products Containing the Oxetane and Related Moieties Present Additional Challenge for Structure Elucidation: a DU8+ Computational Case Study. Kutateladze, A. G.; Holt, T. A.; Reddy, D. S. J. Org. Chem., 2019, 84, (12), 7575-7586. [DOI: 10.1021/acs.joc.9b01005] Featured Article
[150]
Structure Validation of Complex Natural Products: Time to Change the Paradigm. What did Synthesis of Alstofolinine A Prove? Kutateladze, A. G.; Holt, T. A. J. Org. Chem., 2019, 84, (12), 8297-8299. [DOI: 10.1021/acs.joc.9b00969]
[149]
Diastereoselective heterocyclization of geminal bromo-fluoro arylcyclopropanes by nitrosonium tetrafluoroborate: Access to 4-fluorinated isoxazolines and isoxazoles. Bondarenko, O. B.; Komarov, A. I.; Karetnikov, G. L.; Nikolaeva, S. N.; Zyk, N. V.; Holt, T. A.; Kutateladze, A. G. Tetrahedron, 2019, 75, (46), 130666. [DOI: 10.1016/j.tet.2019.130666]
[148]
Reassignments and Corroborations of Oxo-Bridged Natural Products Directed by OSE and DU8+ NMR Computation. Kutateladze, A.G.; Krenske, E.H.; Williams, C.M. Angew. Chem. Int. Ed., 2019, 58, (21), 7107-7112. [DOI: 10.1002/anie.201902777]
[147]
The value of universally available raw NMR data fortransparency, reproducibility, and integrity innatural product research. McAlpine, J.B.; Chen, S.-N.; Kutateladze, A.G.; et. al. Nat. Prod. Rep., 2019, 36, 35-107. [DOI: 10.1039/C7NP00064B]
[146]
Access to 5-Fluoroisoxazoles via the Nitrosation of Geminal Bromo-Fluoro Arylcyclopropanes. Bondarenko, O.B.; Vinogradov, A.A.; Komarov, A.I.; Karetnikov, G.L.; Zyk, N.V.; Holt, T.; Kutateladze, A.G. Tetrahedron, 2019, 75, 2861-2865. [DOI: 10.1016/j.tet.2019.03.054]
[145]
Novel π-Conjugated Systems Based on Pyrimidine N-Oxide. Sedenkova, K.N.; Kolodyazhnaya, J.V.; Vasilenko, D.A.; Gracheva Y.A.; Kharitonoshvili, E.V.; Grishin, Y.K.; Chistov, A.A.; Rybakov, V.B.; Holt, T.; Kutateladze, A.G.; Kuznetsova, T.S.; Milaeva, E.R.; Averina, E.B. Dyes and Pigments, 2019, 164, 72-81. [DOI: 10.1016/j.dyepig.2018.12.067]
[144]
Structural insights into the π-π-π stacking mechanisms and DNA-binding activity of the YEATS domain. Klein, B.J.; Vann, K.R.; Andrews, F.H.; Wang, W.W.; Zhang, J.; Zhang, Y.; Beloglazkina, A.A.; Mi, W.; Li, Y.; Li, H.; Shi, X.; Kutateladze, A.G.; Strahl, B.D.; Liu, W.R.; Kutateladze, T.G. Nat. Commun., 2018, 9, 4574. [DOI: 10.1038/s41467-018-07072-6]
[143]
Addressing the Challenges of Structure Elucidation in Natural Products Possessing the Oxirane Moiety. Kutateladze, A.G.; Kuznetsov, D.M.; Beloglazkina, A. A.; Holt, T. J. Org. Chem., 2018, 83, (15), 8341-8352. [DOI: 10.1021/acs.joc.8b01027] Featured Article. ACS Editors' Choice (made 20 most read JOC articles in August 2018)
[142]
Step-Economical Photoassisted Diversity-Oriented Synthesis: Sustaining Cascade Photoreactions in Oxalyl Anilides to Access Complex Polyheterocyclic Molecular Architectures. Kuznetsov, D.M.; Kutateladze, A.G. J. Am. Chem. Soc., 2017, 139, (46), 16584-16590. [DOI: 10.1021/jacs.7b07598]
[141]
Triquinanes and Related Sesquiterpenes Revisited Computationally: Structure Corrections of Hirsutanols B and D, Hirsutenol E, Cucumin B, Antrodins C−E, Chondroterpenes A and H, Chondrosterins C and E, Dichrocephone A, and Pethybrene. Kutateladze, A.G.; Kuznetsov, D.M. J. Org. Chem., 2017, 82, (20), 10795-10802. [DOI: 10.1021/acs.joc.7b02018] Featured Article. ACS Editors' Choice.
[140]
Structure Determination and Mechanism of Formation of a seco-Moreliane Derivative Supported by Computational Analysis. Chacon Morales, P.A.; Amaro-Luis, J.M.; Kutateladze, A.G. J. Nat. Prod., 2017, 80, (4), 1210-1214. [DOI: 10.1021/acs.jnatprod.7b00041]
[139]
High-Throughput in Silico Structure Validation and Revision of Halogenated Natural Products Is Enabled by Parametric Corrections to DFT-Computed 13C NMR Chemical Shifts and Spin-Spin Coupling Constants. Kutateladze, A.G.; Reddy, D.S. J. Org. Chem., 2017, 82, (7), 3368-3381. [DOI: 10.1021/acs.joc.7b00188]
[138]
A novel withanolide with an unprecedented carbon skeleton from Physalis angulata. Sun, C.-P.; Kutateladze, A.G.; Zhao, F.; Chen, L.-X.; Qiu, F. Org. Biomol. Chem., 2017, 15, 1110-1114. [DOI: 10.1039/c6ob02656g]
[137]
Polyheterocycle-carbohydrate chimeras: photoassisted synthesis of 2,5-epoxybenzoxacines and 2,5-epoxybenzazocine scaffolds and their postphotochemical hydroxylations. Reddy, D.S.; Mukhina, O.A.; Cronk, W.C.; Kutateladze, A.G. Pure Applied Chem., 2017, 89, (2), 259-268. [DOI: 10.1515/pac-2016-0915]
[136]
Photoinduced "Double Click" Cascade Offers Access to Complex Polyheterocycles from Readily Available Isatin-Based Photoprecursors. Cronk, W.C.; Mukhina, O.A.; Kutateladze, A.G. Org. Lett., 2016, 18, (15), 3750-3753. [DOI: 10.1021/acs.orglett.6b01775]
[135]
Structure Revision of an Acorane Sesquiterpene Cordycepol A. Reddy, D.S.; Kutateladze, A.G. Org. Lett., 2016, 18, (19), 4860-4863. [DOI: 10.1021/acs.orglett.6b02341]
[134]
Photoassisted Synthesis of Complex Molecular Architectures: Dearomatization of Benzenoid Arenes with Aza-o-xylylenes via an Unprecedented [2+4] Reaction Topology. Kuznetsov, D.M.; Mukhina, O.A.; Kutateladze, A.G. Angew. Chem., 2016, 55, (24), 6988-6991. [DOI: 10.1002/anie.201602288]
[133]
Structure Revision of Decurrensides A-E Enabled by the RFF Parametric Calculations of Proton Spin-Spin Coupling Constants. Kutateladze, A.G. J. Org. Chem., 2016, 81, (18), 8659-8661. [DOI: 10.1021/acs.joc.6b01855]
[132]
Oxazolines as Dual Function Traceless Chromophores and Chiral Auxiliaries: Enantioselective Photoassisted Synthesis of Polyheterocyclic Ketones. Mukhina, O.A.; Kutateladze, A.G. J. Am. Chem. Soc., 2016, 138, (7), 2110-2113. [DOI: 10.1021/jacs.5b12690]
[131]
Computational structure revision of a longipinane derivative meridane. Reddy, D.S.; Kutateladze, A.G. Tetrahedron Lett., 2016, 57, (42), 4727-4729. [DOI: 10.1016/j.tetlet.2016.09.030]
[130]
Photoassisted access to Complex Polyheterocycles Containing a β-lactam moiety. Umstead, W.J.; Mukhina, O.A.; Kutateladze, A.G. J. Photochem. Photobiol. A: Chem., 2016, 329, 182-188. [DOI: 10.1016/j.jphotochem.2016.07.004]
[129]
Beyond the Dimer and Trimer: Tetraspiro[2.1.25.1.29.1.213.13]hexadecane-1,3,5,7-tetraone - the Cyclic Tetramer of Carbonylcyclopropane. Sedenkova, K.N.; Averina, E.B.; Grishin, Y.K.; Andriasov, K.S.; Stepanova, S.A.; Roznyatovsky, V. A.; Kutateladze, A.G.; Rybakov, V.B.; Albov, D.V.; Kuznetsova, T.S.; Zefirov, N.S. Chem. Eur. J., 2016, 22, (12), 3996-3999. [DOI: 10.1002/chem.201600140]
[128]
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications. Kumar, N.N.B.; Kutateladze, A.G. Org. Lett., 2016, 18, (3), 460-463. [DOI: 10.1021/acs.orglett.5b03503]
[127]
Amino Azaxylylenes Photogenerated from o-Amido Imines: Photoassisted Access to Complex Spiro-Polyheterocycles. Mukhina, O.A.; Kuznetsov, D.M.; Cowger, T.M.; Kutateladze, A.G. Angew. Chem. Int. Ed., 2015, 54, (39), 11516-11520. [DOI: 10.1002/anie.201504455]
[126]
Relativistic Force Field: Parametrization of 13C-1H Nuclear Spin-Spin Coupling Constants. Kutateladze, A.G.; Mukhina, O.A. J. Org. Chem., 2015, 80, (21), 10838-10848. [DOI: 10.1021/acs.joc.5b02001]
[125]
Photoinduced Cycloadditions in the Diversity-Oriented Synthesis Toolbox: Increasing Complexity with Straightforward Postphotochemical Modifications. Umstead, W.J.; Mukhina, O.A.; Kumar, N.N.B.; Kutateladze, A.G. Aust. J. Chem., 2015, 68, 1672-1681. [DOI: 10.1071/CH15266]
[124]
Computationally driven reassignment of the structures of aldingenins A and B. Mukhina O.A.; Koshino, H.; Crimmins M.T.; Kutateladze, A.G. Tetrahedron Lett. , 2015, 56, 4900-4903. [DOI: 10.1016/j.tetlet.2015.06.078]
[123]
Minimalist Relativistic Force Field: Prediction of Proton-Proton Coupling Constants in 1H NMR Spectra is Perfected with NBO Hybridization Parameters. Kutateladze, A.G.; Mukhina, O.A. J. Org. Chem., 2015, 80, (10), 5218-5225. [DOI: 10.1021/acs.joc.5b00619]
[122]
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-Oxirane Moiety. Kumar, N.N.B.; Kuznetsov, D.M.; Kutateladze, A.G. Org. Lett. , 2015, 17, (3), 438-441. [DOI: 10.1021/ol5033909]
[121]
Conformationally Constrained Penta(hetero)cyclic Molecular Architectures via Photoassisted Diversity-Oriented Synthesis. Umstead, W.J.; Mukhina, O.A.; Kutateladze, A.G. Eur. J. Org. Chem., 2015, (10), 2205-2213. [DOI: 10.1002/ejoc.201403620]
[120]
An acetyl-methyl switch drives a conformational change in p53. Tong, Q.; Mazur, S.J.; Rincon-Arano, H.; Rothbart, S.; Kuznetsov, D.M.; Cui, G.; Liu, W.H.; Gete, Y.; Klein, B.J.; Jenkins, L.; Mer, G.; Kutateladze, A.G.; Strahl, B.D.; Groudine, M.; Appella, E.; Kutateladze, T.G. Structure, 2015, 23, (2), 322-331. [DOI: 10.1016/j.str.2014.12.010]
[119]
Photoassisted Diversity-Oriented Synthesis: Accessing 2,6-Epoxyazocane (Oxamorphan) Cores. Mukhina, O.A.; Kumar, N.N.B.; Cowger, T.M.; Kutateladze, A.G. J. Org. Chem., 2014, 79, (22), 10956-10971. [DOI: 10.1021/jo5019848]
[118]
Relativistic Force Field: Parametric Computations of Proton-Proton Coupling Constants in 1H NMR Spectra. Kutateladze, A.G.; Mukhina, O.A. J. Org. Chem., 2014, 79, (17), 8397-8406. [DOI: 10.1021/jo501781b]
[117]
Intramolecular Cycloadditions of Photogenerated Azaxylylenes: an Experimental and Theoretical Study. Mukhina, O.A.; Cronk, W.C.; Kumar, N.N.B.; Sekhar, M.; Samanta, A.; Kutateladze, A.G. J. Phys. Chem. A., 2014, 118, (45), 10487-10496. [DOI: 10.1021/jp504281y]
[116]
symm-Tetramethylenecyclooctane: En Route to Polyspirocycles. Averina, E.B.; Sedenkova, K.N.; Bakhtin, S.G.; Grishin, Y.K.; Kutateladze, A.G.; Roznyatovsky, V.A.; Rybakov, V.B.; Butov G.M.; Kuznetsova, T.S.; Zerfirov, N.S. J. Org Chem., 2014, 79, (17), 8163-8170. [DOI: 10.1021/jo501380y]
[115]
Photoactive Spatial Proximity Probes for Binding Pairs with Epigenetic Marks. Ezhov, R.N.; Metzel, G.A.; Mukhina, O.A.; Musselman, C.A.; Kutateladze, T.G; Gustafson, T.P.; Kutateladze, A.G. J. Photochem. Photobiol. A: Chemistry, 2014, 290, 101-108. [DOI: 10.1016/j.jphotochem.2014.06.014]
[114]
Intramolecular Photoassisted Cycloadditions of Azaxylylenes and Post-Photochemical Capstone Modifications via Suzuki Coupling Provide Access to Complex Polyheterocyclic Biaryls. Cronk, W.C.; Mukhina, O.A.; Kutateladze, A.G. J. Org. Chem., 2014, 79, (3), 1235-1246. [DOI: 10.1021/jo4026447]
[113]
Photoinduced signal amplification through externally sensitized photofragmentation in masked photosensitizers. Kutateladze, A. G.; Kurchan, A. N.; Kottani, R.; Majjigapu, J. R. R. US 8,735,167 B2, 2014, May27.
[112]
Photoassisted Synthesis of Enantiopure Alkaloid Mimics Possessing Unprecedented Polyheterocyclic Cores. Kumar, N.N.B.; Mukhina, O.A.; Kutateladze, A.G. J. Am. Chem. Soc., 2013, 135, (26), 9608-9611. [DOI: 10.1021/ja4042109]
[111]
Photoassisted Access to Enantiopure Conformationally Locked Ribofuranosylamines Spiro-Linked to Oxazolidino- Diketopiperazines. Nandurkar, N.S.; Kumar, N.N.B.; Mukhina, O.A.; Kutateladze, A.G. ACS Combinatorial Sci., 2013, 15, (1), 73-76. [DOI: 10.1021/co3001296]
[110]
Photoinduced Intramolecular Cyclopentanation vs Photoprotolytic Oxametathesis in Policyclic Alkenes Outfitted with Conformationally Constrained Aroylmethyl Chromophores. Valiulin, R.A.; Arisco, T.M.; Kutateladze, A.G. J. Org. Chem., 2013, 78, (5), 2012-2025. [DOI: 10.1021/jo301909j]
[109]
Cascade Transformations Involving Thiocarbonyls: Photoassisted Access to Bicyclic Thiiranes and Oxapentalenes. Valiulin, R.A.; Kumar, N.N.B.; Kuznetsov, D.M.; Kutateladze, A.G. J. Sulfur Chem., 2013, 34, (1-2), 209-221. [DOI: 10.1080/17415993.2012.731065]
[108]
Three-Component Heterocyclization of gem-Bromofluorocyclopropanes with NOBF4: Access to 4-Fluoropyrimidine N-Oxides Sedenkova, K.N.; Averina, E.B.; Grishin, Y.K.; Kutateladze, A.G.; Rybakov, V.B.; Kuznetsova, T.S.; Zefirov, N.S. J. Org. Chem., 2012, 77, (21), 9893-9899. [DOI: 10.1021/jo301880m]
[107]
Externally Sensitized Deprotection of PPG-Masked Carbonyls as a Spatial Proximity Probe in Photoamplified Detection of Binding Events. Gustafson, T.P.; Metzel, G.A.; Kutateladze, A.G. Photochem. Photobiol. Sci., 2012, 11, (3), 564-577. [DOI: 10.1039/C2PP05326H]
[106]
Heterocyclization of Electrophilic Alkenes with Tetranitromethane Revisited: Regiochemistry and the Mechanism of Nitroisoxazoles Formation. Averina, E.B.; Samoilichenko, Y.V.; Volkova, Y.A.; Grishin, Y.K.; Rybakov, V.B.; Kutateladze, A.G.; Elyashberg, M.E.; Kuznetsova, T.S.; Zefirov, N.S. Tetrahedron Lett., 2012, 53, (12), 1472-1475. [DOI: 10.1016/j.tetlet.2012.01.039]
[105]
Rapid Photoassisted Access to N,O,S-Polyheterocycles with Benzoazocine and Hydroquinoline Cores via Intramolecular Cycloadditions of Photogenerated Azaxylylenes Mukhina, O.A.; Kumar, N.N.B.; Arisco, T.M.; Valiulin, R.A.; Metzel, G.A.; Kutateladze, A.G. Angew. Chem. Int. Ed. , 2011, 50, (40), 9423-9428. [DOI: 10.1002/anie.201103597] Angewandte's Hot Paper (click here)
[104]
Photochemically Amplified Detection of Molecular Recognition Events: An Ultra-Sensitive Fluorescence Turn-Off Binding Assay. Gustafson, T.P.; Metzel, G.A.; Kutateladze, A.G. Org. Biomol. Chem., 2011, 9, (13), 4752-4755. [DOI: 10.1039/C1OB05289F] Selected as an OBC HOT Article (click here)
[103]
Double-tandem [4π+2π]-[2π+2π]-[4π+2π]-[2π+2π] Synthetic Sequence with Photoprotolytic Oxametathesis and Photoepoxidation in the Chromone Series. Valiulin, R.A.; Arisco, T.M., Kutateladze, A.G. J. Org. Chem., 2011, 76, (5), 1319-1332. [DOI: 10.1021/jo102221q]
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Strained to the Limit: When a Cyclobutyl Moiety Becomes a Thermodynamic Sink in a Protolytic Ring Opening of Photogenerated Oxetanes Valiulin, R.A.; Arisco, T.M., Kutateladze, A.G. Org. Lett., 2010, 12, (15), 3398-3401. [DOI: 10.1021/ol101297b]
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First Example of Intramolecular [2π+2π] Alkene-Arene Photocyclization in the Chromone Series and its Synthetic Utility Valiulin, R.A.; Kutateladze, A.G. Tetrahedron Lett., 2010, 51, (29), 3803-3806. [DOI: 10.1016/j.tetlet.2010.05.078]
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Harvesting the Strain Installed by a Patern?B?hi Step in a Synthetically Useful Way: High Yielding Photo-Protolytic Oxametathesis in Polycyclic Systems. Valiulin, R.A.; Kutateladze, A.G. Org. Lett., 2009, 11, (17), 3886-3889. [DOI: 10.1021/ol901456m]
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Effect of Intramolecular Patern?B?hi Reaction on the Thermodynamics and Kinetics of Nearly Degenerate [3,3]-Sigmatropic Shift in Fluxional Polycycles. Valiulin, R.A.; Dressen, D.G.; Riggs, J.R.; Habte, F.M.; Kutateladze, A.G. J. Org. Chem., 2009, 74, (9), 3484-3490. [DOI: 10.1021/jo9003822]
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Interaction of Radical Pairs Through-Bond and Through-Space: Scope and Limitations of the Point-Dipole Approximation in Electron Paramagnetic Resonance Spectroscopy. Riplinger, C.; Kao, J.; Rosen, G.; Kathirvelu, V.; Eaton, G.; Eaton, S.; Kutateladze, A.; Neese, F. J. Am. Chem. Soc., 2009, 131, (29), 10092-10106. [DOI: 10.1021/ja901150j]
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A Peculiar Quenching Concentration Dependence of Photoinduced Fragmentation in Dithiane-Carbonyl Adducts: A Mechanistic Experimental and Theoretical Study. Valiulin, R.A.; Lakkakula, S.; Kutateladze, A.G. J. Photochem. Photobiol. A Chemistry, 2009, 206, 80-86. [DOI: 10.1016/j.jphotochem.2009.05.016]
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Membrane insertion of the FYVE domain is modulated by pH. He, J.; Vora, M.; Haney, R.M.; Filonov, G.S.; Musselman, C.A.; Burd, C.G.; Kutateladze, A.G.; Verkhusha, V.V.; Stahelin, R.A.; Kutateladze, T.G. Proteins, 2009, 76, (4), 852-860. [DOI: 10.1002/prot.22392]
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Effect of beta-Alkylthioethyl Substitution in 1,3-Dithianes: Quasi-Anchimeric Assistance in Photoinduced Electron Transfer? Valiulin, R.A.; Kutateladze, A.G. J. Org. Chem., 2008, 73, (16), 6393-6396. [DOI: 10.1021/jo800938d]
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Photolabile Amphiphiles with Fluorogenic Thioxanthone-Dithiane Functionality: Synthesis and Photoinduced Fragmentation in Micelles. Ezhov, R.N.; Rozhkov, V.V.; Majjigapu, J.R.R.; Kutateladze, A.G. J. Sulf. Chem., 2008, 29, (3-4), 389-400. [DOI: 10.1080/17415990802027289]
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Protocols on safety, efficacy, standardization, and documentation of herbal medicine. Mosihuzzaman, M.; et al. Pure Appl. Chem. , 2008, 80, (10), 2195-2230.
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2,6,7-Trithiabicyclo[2.2.2]octanes as Promising Photolabile Tags for Combinatorial Encoding. Valiulin, R.A.; Kutateladze, A.G. J. Org. Chem., 2008, 73, (1), 335-338. [DOI: 10.1021/jo702091e]
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Photoamplification and Multiple Tag Release in a Linear Peptide-Based Array of Dithiane Adducts Majjigapu, K.; Majjigapu, J.R.R.; Kutateladze, A.G. Angew. Chem., 2007, 46, (32), 6137-6140. [DOI: 10.1002/anie.200701512]
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Interrupted Oligomerization Revisited: Simple and Efficient One Pot Multicomponent Approach to Versatile Synthetic Intermediates. Valiulin, R.A.; Halliburton, L.M.; Kutateladze, A.G. Org. Lett., 2007, 9, (20), 4061-4063. [DOI: 10.1021/ol701847b]
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Method for Encoding and Screening Combinatorial Libraries. Kottani, R.; Valiulin, R. A.; Majjigapu, J. R. R., Kutateladze, A. G. WO2006US61728, 2007, June_21, esp@cenet
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Photoactive Barbiturate Receptors: An Ultimate Lock-and-Key System in Which the Key Unlocks the Lock. Lakkakula, S.; Mitkin, O.D.; Valiulin, R.A.; Kutateladze, A.G. Org. Lett., 2007, 9, (6), 1077-1079. [DOI: 10.1021/ol0700153]
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Bis-(4-(2-pyridylmethyleneiminophenyl)disulfide - a Chelating Ligand Capable of Self Assembly on Gold Surface and Its Complexes with M(BF4)2 and M(ClO4)2; M = Co, Cu and Ni. Experimental and Theoretical Study. Beloglazkina, E. K.; Majouga, A. G.; Zyk, N. V.; Rakhimov, R. D.; Yaminsky, I. V.; Gorelkin, P.; Kiselev, G. A.; Kutateladze, A. G. Thin Solid Films, 2007, 515, (11), 4649-4661. [DOI: 10.1016/j.tsf.2006.12.131]
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Photolabile system with instantaneous fluorescence reporting function. Kutateladze, A. G.; Kurchan, A. N.; Kottani, R.; Majjigapu, J. R. R. WO2007008471 , 2007, January_18, esp@cenet
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Glossary of Terms Used In Photochemistry, 3d Edition Braslavsky S.E. et al. Pure Appl. Chem., 2007, 79, (3), 293-465. [DOI: 10.1351/pac200779030293]
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Photoinduced Signal Amplification Through Controlled Externally Sensitized Fragmentation in Masked Sensitizers. Kottani, R.R.; Majjigapu, J.R.R.; Kurchan, A.N.; Majjigapu, K.; Gustafson, T.P.; Kutateladze, A.G. J. Am. Chem. Soc., 2006, 128, (46), 14794-14795. [DOI: 10.1021/ja066692u]
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Direct Screening of Solution Phase Combinatorial Libraries Encoded with Externally Sensitized Photolabile Tags. Kottani, R.; Valiulin, R. A.; Kutateladze, A. G. Proc. Natl. Acad. Sci. USA, 2006, 103, (38), 13917-13921. [DOI: 10.1073/pnas.0606380103]
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Conformational Analysis of Spiro-Bis-Dithiepins: a Peculiar Case of Axial Chirality Wade, E.O.; Valiulin, R.A.; Ruybal, L.A.; Kutateladze, A.G. Org. Lett., 2006, 8, (22), 5121-5124. [DOI: 10.1021/ol062172s]
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When Ethyl is Infinitely Different from Methyl: Double Addition of Lithiated Dithianes to Aromatic Carboxylates Revisited. Valiulin, R. A.; Kottani, R.; Kutateladze, A. G. J. Org. Chem, 2006, 71, (13), 5047-5049. [DOI: 10.1021/jo060780f]
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Externally Sensitized Mesolytic Fragmentations in Dithiane-Ketone Adducts. Gustafson, T. P.; Kurchan, A. N.; Kutateladze, A. G. Tetrahedron, 2006, 62, (27), 6574-6580. [DOI: 10.1016/j.tet.2006.03.065]
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Release and Report: A New Photolabile Caging System with a Two-photon Fluorescence Reporting Function. Majjigapu, J. R. R.; Kurchan, A. N.; Kottani, R.; Gustafson, T. P.; Kutateladze, A. G. J. Am. Chem. Soc., 2005, 127, (36), 12458-12459. [DOI: 10.1021/ja053654m]
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Investigation of the Binding Geometry of a Peripheral Membrane Protein. Brunecky, R.; Lee, S.; Rzepecki, P.W.; Overduin, M.; Prestwich, G.D.; Kutateladze, A.G.; Kutateladze, T.G. Biochem., 2005, 44, (49), 16064-16071. [DOI: 10.1021/bi051127+]
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Dithiane and Trithiane-Based Photolabile Molecular Linkers Equipped with Amino-Functionality: Synthesis and Quantum Yields of Fragmentation. Kurchan, A. N.; Mitkin, O. D.; Kutateladze, A. G. J. Photochem. Photobiol. A: Chemistry, 2005, 171, 121-129. [DOI: 10.1016/j.jphotochem.2004.09.014]
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Computational Methods in Photochemistry. Kutateladze, A. G., Editor; CRC Press, Molecular and Supramolecular Photochemistry, 2005, Vol 13.
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Toward Parameterization of Spin-Orbit Coupling in Triplet Organic Diradicals Separated by a Partially Conjugated Spacer. Kutateladze, A.G.; McHale, W.A.Jr. ARKIVOC, 2005, IV, 88-101.
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Dithiane, Trithiane and Dithiazane-Based Photolabile Scaffolds for Molecular Recognition: Mechanism and Efficiency of the Photoinduced Fragmentation in Aqueous Reductive Environments. Kutateladze, A.G; Kottani, R.; Kurchan, A. N.; Majjigapu, J. R. R.; Shirk, S. M. Phosph. Sulf. Silicon, 2005, 180, (5-6), 1379-1384.
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Addition of Lithiated 5 Hydroxymethyl-1,3 Dithiane to Benzaldehyde: HMPA-Controlled trans-Stereoselectivity Li, Z.; Kurchan, A. N.; Kutateladze, A. G. Org. Lett., 2004, 6, (8), 1213-1216. [DOI: 10.1021/ol0499497]
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Dithiane and Trithiane-Based Photocleavable Systems for Molecular Assembly and Disassembly. Kurchan, A. N.; Shirk, S. M.; Kutateladze, A. G. The Spectrum, 2004, 17, (4), 20-25.
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Multivalent Mechanism of Membrane Insertion by the FYVE Domain. Kutateladze, T. G.; Capelluto, D. G. S.; Ferguson, C. G.; Cheever, M. L.; Kutateladze, A. G.; Prestwich, G. D.; Overduin, M. J. Biol. Chem., 2004, 279, (4), 3050-3057.
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Anomalous C-C Bond Cleavage in Sulfur-Centered Cation Radicals Containing Vicinal Hydroxy Group. Li, Z.; Kutateladze, A. G. J. Org. Chem., 2003, 68, (21), 8236-8239. [DOI: 10.1021/jo035001z]
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ICP21 Report. Kutateladze, A. G. IAPS Newsletter, 2003, 26, (1), 11-15.
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Novel Dithia-aza-norbornanes as "Stiff" Bicyclic Dithiazines. Kurchan, A. N.; Wade, E.; Kutateladze, A. G. Synlett , 2003, (11), 1731-1733. [DOI: 10.1055/s-2003-41431]
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Dithiane-Based Photolabile Amphiphiles: Toward Photolabile Liposomes. Li, Z.; Wan, Y.; Kutateladze, A. G. Langmuir, 2003, 19, (16), 6381-6391. [DOI: 10.1021/la034188m]
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Photolabile Calixarene-Based Rosette. Li, Z.; Chiu, H.; Kutateladze, A. G. Can. J. Chem., 2003, 81, (6), 807-810. [DOI: 10.1139/V03-057]
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Amino Acid-Based Dithiazines: Synthesis and Photofragmentation of Their Benzaldehyde Adducts. Kurchan, A. N.; Kutateladze, A. G. Org. Lett., 2002, 4, (23), 4129-4131. [DOI: 10.1021/ol0268790]
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Liposomes from Novel Photolabile Phospholipids: Light-Induced Unloading of Small Molecules as Monitored by PFG NMR. Wan, Y.; Angleson, J. K.; Kutateladze, A. G. J. Am. Chem. Soc., 2002, 124, (20), 5610-5611. [DOI: 10.1021/ja016874i]
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Synthesis and Liquid Membrane Transport Properties of Photolabile Molecular Clips Based on Dithiane-Spiro-Crown Ethers. Barnhurst, L. A.; Kutateladze, A. G. Org. Lett., 2001, 3, (17), 2633-2635. [DOI: 10.1021/ol016309k]
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Conformational Analysis of Singlet-Triplet State Mixing in Paterno-Buchi Diradicals. Kutateladze, A. G. J. Am. Chem. Soc., 2001, 123, (38), 9279-9282. [DOI: 10.1021/ja016092p]
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Synthesis of Dithiane-Based Photolabile Molecular Systems. Mitkin, O.; Wan, Y.; Kurchan, A.; Kutateladze, A. Synthesis, 2001, (8), 1133-1142.
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Photoinduced C-C Bond Cleavage in Dithiane-Carbonyl Adducts: A Laser Flash Photolysis Study. Vath, P.; Falvey, D. E.; Barnhurst, L. A.; Kutateladze, A. G. J. Org. Chem., 2001, 66, (8), 2886-2890. [DOI: 10.1021/jo010102n]
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Dithiane and Trithiane-Based Photolabile Scaffolds for Molecular Recognition. Mitkin, O. D.; Kurchan, A. N.; Wan, Y.; Schiwal, B. F.; Kutateladze, A. G. Org. Lett., 2001, 3, (12), 1841-1844. [DOI: 10.1021/ol015933u]
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Photoinduced 1,3-Proton Shift in Methyldithiepines as a Potential Way of Modulating Hyperpolarizabilities. Wan, Y.; Kurchan, A. N.; Kutateladze, A. G. J. Org. Chem., 2001, 66, (5), 1894-1899. [DOI: 10.1021/jo005707i]
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Determination of the Position of the Conformational Equilibrium of a trans-1,2-Disubstituted Cyclohexane by NMR Spectroscopy. An Experiment in Physical Organic Chemistry for Undergraduate Students. Kutateladze, A. G.; Hornback J. M. J. Chem. Ed., 2001, 78, (1), 81-82.
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Molecular Assembly and Disassembly: Novel Photolabile Molecular Hosts. Wan, Y.; Mitkin, O.; Barnhurst L.; Kurchan, A.; Kutateladze, A. Org. Lett., 2000, 2, (24), 3817-3819. [DOI: 10.1021/ol006692d]
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Direct Transformation of 1,3-Dihalides into Dithianes and Dithiepins via a Novel One Pot Reaction with Carbon Disulfide and Sodium Borohydride. Wan, Y.; Kurchan, A. N.; Barnhurst L. A.; Kutateladze, A. G. Org. Lett., 2000, 2, (8), 1133-1135. [DOI: 10.1021/ol005705k]
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Efficient Electrochemical Deprotection of Carboxylic and Amino Acids from Their 2-(Hydroxymethyl)-1,3-dithiane (Dim) Esters. Barnhurst, L. A.; Wan, Y.; Kutateladze A. G. Org. Lett. , 2000, 2, (6), 799-801. [DOI: 10.1021/ol005537w]
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Photooxidation of Methyldithiepins into Dithiepin Carboxaldehydes in Carbon Tetrachloride. Wan Y., Barnhurst, L. A.; Kutateladze A. G. Org. Lett. , 1999, 1, (6), 937-939. [DOI: 10.1021/ol990870p]
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Reactions of Nitrosonium Ethyl Sulfate with Olefins and Dienes: An Experimental and Theoretical Study. Zyk, N. V.; Nesterov, E. E.; Khlobystov, A. N.; Zefirov, N. S.; Barnhurst, L. A.; Kutateladze, A. G. J. Org. Chem. , 1999, 64, (19), 7121-7128. [DOI: 10.1021/jo990679t]
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An Efficient Photo-SET-Induced Cleavage of Dithiane-Carbonyl Adducts and Its Relevance to the Development of Photoremovable Protecting Groups for Ketones and Aldehydes. McHale, W. A.; Kutateladze A. G. J. Org. Chem. , 1998, 63, (26), 9924-9931. [DOI: 10.1021/jo981697y]
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Tin-Free Reductive Photochemical Carboxymethylation of Olefins with α-Alkylthioacetates. Deng, L. X.; Kutateladze, A. G. Tetrahedron Lett. , 1997, 38, (44), 7829-7832.
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New Approaches to Singlet-Triplet Spin-Orbit Coupling in Photochemistry and Diradical Chemistry; Mechanistic and Exploratory Organic Photochemistry. Zimmerman, H. E.; Kutateladze, A.G. J. Am. Chem. Soc. , 1996, 118, (1), 249-250. [DOI: 10.1021/ja953052a]
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S-Tosylthiosulfenamides as electrophilic sulfosulfenylating reagents. Zyk N.V.; Beloglazkina E.K.; Alabugin I.V.; Kutateladze A.G.; Zefirov N.S. Bulletin of Moscow State University (Vestnik MGU), Ser.Khimia, , 1996, 37, (1), 68-70.
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Novel Dissection Analysis of Spin-Orbit Coupling in the Type-B Cyclohexenone Photorearrangement. What Controls Photoreactivity? Mechanistic and Exploratory Organic Photochemistry. Zimmerman, H.E.; Kutateladze, A.G. J. Org. Chem. , 1995, 60, (19), 6008.
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Sulfoxylic Acid Derivatives as Novel Sulfenylating Reagents. Vatsadze, S.Z.; Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G. Phosphorus, Sulfur, and Silicon , 1994, 95, 333.
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Excited State Reactivity as a Function of Diradical Structure. Evidence for Two Triplet Cyclopropyl-dicarbinyl Diradical Intermediates With Differing Reactivity. Zimmerman, H.E.; Kutateladze, A.G.; Maekawa, Y.; Mangette, J.E. J. Am. Chem. Soc. , 1994, 116, (21), 9795.
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Electrophilic Sulfamatoselenenylation of Olefins. Zyk, N.V., Alabugin, I.V.; Kutateladze, A.G.; Kice, J.L.; Zefirov, N.S. Dokl. Acad. Nauk SSSR , 1994, 317, (2), 208.
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A One-pot Trifunctionalization of Olefins with Benzeneseleninic and Trifluoroacetic Anhydrides Using a Commonly Undesirable Side Reaction as a Key Step. Kutateladze, A.G.; Kice, J.L.; Kutateladze, T.G.; Zefirov, N.S. J. Org. Chem., 1993, 58, 995.
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Thiosulfonates: synthesis, reactions and practical application. (Review). Zefirov, N.S.; Zyk, N.V.; Beloglazkina, E.K.; Kutateladze, A.G. Sulfur Reports, 1993, 14, 223.
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Phenylethynesulfenyl sulfamate - a new sulfenylating reagent. Denisko, O.V.; Kutateladze, A.G.; Zyk, N.V.; Zefirov, N.S. Sulfur Lett., 1993, 14, 341.
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The Markedly Enhanced Basicity of Selenenamides vs. Sulfenamides and the Mechanism of the Methanolysis of o-Nitro- and 2,4,6-Tri-tert-butylbenzeneselenenamides. Kice, J.L; Kutateladze, A.G. J. Org. Chem., 1993, 58, 917.
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S-Tosylsulfenyl Chloride - the First Representative of a New Class of Sulfur Halides. Kutateladze, A.G.; Beloglazkina, E.K.; Zyk, N.V.; Zefirov, N.S. Izv. Akad. Nauk SSSR, Ser. Khim. , 1992, (5), 1217.
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Sulfato-sulfenylation of Olefins by Ethyl Phenylsulfenate in the Presence of Sulfur Trioxide. Zefirov, N.S.; Zyk, N.V.; Lapin, Yu.A.; Kutateladze, A.G.; Ugrak, B.I. Zh. Org. Chem. , 1992, 28, (6), 1126.
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Superelectrophilic Selenium. A New Simple Method for Generation of Areneselenenyl Trifluoroacetates and Triflates. Kutateladze, A.G.; Kice, J.L.; Kutateladze, T.G.; Zefirov, N.S.; Zyk, N.V. Tetrahedron Lett., 1992, 33, 1949.
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Reactions of sulfenic and sulfoxylic acid derivatives with olefins in the presence of sulfur trioxide and its complexes. (Review). Kutateladze, A.G.; Zefirov, N.S.; Zyk, N.V. Sulfur Reports, 1992, 11, (2), 233. [CA: 117, 130842w]
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Mechanism of Nucleophilic Substitution Reactions of o-Nitrobenzene-sulfenamides: Evidence for a Substitution Proceeding through a Sulfuranide Intermediate. Kice, J.L.; Kutateladze, A.G. J. Org. Chem., 1992, 57, 3298.
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A Simple New Synthesis of Thiobisamines. Kutateladze, T.G.; Kice, J.L.; Kutateladze, A.G.; Zefirov, N.S.; Zyk, N.V. J. Org. Chem. , 1991, 56, 5235.
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S-Tosylsulfenamides as new electrophilic reagents for sulfation-sulfenylation. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Beloglazkina, E.K. Izv. Akad. Nauk SSSR, Ser. Khim. , 1991, (11), 2623. [CA: 116, 105254c]
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Amino sulfenyl halides in synthesis of unsymmetrical diastereomeric sulfamato sulfides. Kutateladze, A.G.; Zyk, N.V.; Denisko, O.V.; Zefirov, N.S. Zh. Org. Khim. , 1991, 27, (3), 659. [CA: 115, 159068t]
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Synthesis of thiophenes from acyl chloride - allyl chloride adducts. Mamedov, E.I.; Ismailov, A.G.; Zyk, N.V.; Kutateladze, A.G.; Zefirov, N.S. Sulfur Lett., 1991, 12, (3), 109. [CA: 114, 185180x]
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Stereospecific sulfenylation of tetrafluorobenzobicyclo[2.2.2]octatriene (TFBBO). The structure of the ethyl sulfate of exo-12-phenylthio-3,4,5,6-tetrafluorotricyclo- [6.2.2.02,7]dodeca-2,4,6,9-tetraen-endo-11-ol. Zefirov, N.S.; Zyk, N.V.; Lapin, Yu.A.; Kutateladze, A.G.; Panov, V.N.; Goncharov, A.V.; Yufit, D.S.; Struchkov, Yu.T. Sulfur Lett., 1991, 12, (3), 103. [CA: 114, 184863k]
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Difunctionalization of olefins with N-chloroamines in the presence of potassium pyrosulfate and bis(trimethylsilyl)sulfate. Zyk, N.V.; Mendeleeva, E.A.; Kutateladze, A.G.; Zefirov, N.S. Dokl. Acad. Nauk SSSR , 1990, 313, (5), 1138. [CA: 114, 184850d]
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Vinylsulfenylation of olefins via sulfonate activation. Kutateladze, A.G.; Zyk, N.V.; Denisko, O.V.; Zefirov, N.S. Izv. Acad. Nauk SSSR, Ser. Khim. , 1990, (7), 1689. [CA: 113, 211924u]
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Aminothiosulfonates - electrophilic synthones in the synthesis of thiosulfonates. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Butina, E.K. Zh. Org. Khim., 1990, 26, (10), 2225.
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Reaction of sulfenamides with olefins in the presence of potassium pyrosulfate. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Ignatchenko, E.S. Zh. Org. Khim. , 1990, 26, (3), 670. [CA: 113, 151944p]
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Reaction of sulfenamides with cycloolefins in the presence of sulfamic acid, NH3-SO3. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Butina, E.K. Zh. Org. Khim., 1990, 26, (3), 671. [CA: 113, 151945q]
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Sulfur trioxide mediated additon of N-chlorourethanes to carbon-carbon double bond. Zyk, N.V.; Mendeleeva, E.A.; Kolbasenko, S.I.; Kutateladze, A.G.; Zefirov, N.S. Izv. Acad. Nauk SSSR, Ser. Khim., 1989, (12), 2869. [CA: 112, 216270s]
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Aminosulfenylation of olefins by sulfenamides in the presence of sulfamic acid, NH3-SO3. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Butina, E.K.; Vatsadze, S.Z. Izv. Acad. Nauk SSSR, Ser. Khim., 1989, (12), 2870. [CA: 113, 5792w]
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Insertion reaction of N-sulfonylmethylamine into the sulfur-nitrogen bond of sulfenamides. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Ignatchenko, E.S.; Denisko, O.V. Zh. Org. Khim., 1989, 25, (7), 1576. [CA: 112, 20730x]
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Sulfate-activated nitration of tetrafluorobenzobarrelene. Crystal and molecular structure of the ethyl sulfate derivative of anti-8-nitro-3,4-tetrafluorobenzobicyclo[3.2.1]octa-3,6-dien-exo-2-ol, C14H11F4NO6S. Zefirov, N.S.; Zyk, N.V; Lapin, Yu.A.; Kutateladze, A.G.; Panov, V.N.; Goncharov, A.V.; Kurkutova, E.N.; Struchkov, Yu.T. Dokl. Acad. Nauk SSSR, 1989, 307, (2), 378. [CA: 112, 178297w]
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Phenylsulfenyl sulfate: a new sulfenylating reagent. Zyk, N.V.; Lapin, Yu.A.; Kutateladze, A.G.; Zefirov, N.S. Zh. Org. Khim., 1989, 25, (1), 198. [CA: 111, 133716v]
[19]
Aminosulfenylation of olefins by sulfenamides and thio-bis-amines in the presence of pyridine - sulfur trioxide. Rare example of stability of ?-sulfidoalcohol N,N-dimethylsulfamate. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Ugrak, B.I.; Struchkov, Yu.T.; Potekhin, K.A., Maleev, A.V. Dokl. Acad. Nauk SSSR , 1988, 301, (6), 1385. [CA: 111, 6981]
[18]
Bifunctionalization of olefins by ethyl nitrate in the presence of sulfur trioxide. Zefirov, N.S.; Zyk, N.V.; Lapin, Yu.A.; Kutateladze, A.G. Sulfur Lett., 1988, 8, (3), 143. [CA: 111, 153251t]
[17]
Vicinal nitrato sulfates. Zyk, N.V.; Lapin, Yu.A.; Kutateladze, A.G.; Zefirov, N.S. Zh. Org. Khim. , 1988, 24, (4), 889. [CA: 110, 23379j]
[16]
Sulfonate-activated cleavage of the cyclopropane fragment of quadricyclane. Zyk, N.V.; Kolbasenko, S.I.; Kutateladze, A.G.; Lapin, Yu.A. Zh. Org. Khim., 1988, 24, (6), 1208. [CA: 110, 134766c]
[15]
Preparation of chlorobromohydrocarbons. Zefirov, N.S.; Zyk, N.V.; Kolbasenko, S.I.; Kutateladze, A.G.; Chizhov, A.O. U.S.S.R. Patent, SU-1351039, June 8, 1987,
[14]
X-ray structural investigation of the addition product of thio-bis-morpholine to norbornene in the presence of the sulfur trioxide - pyridine complex. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Potekhin, K.A.; Struchkov, Yu.T. Sulfur Lett., 1987, 6, (5), 139. [CA: 108, 112356a]
[13]
Thiobis(amines) in the synthesis of thiobis(alkanol) disulfamates. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Lapin, Yu.A. Zh. Org. Khim., 1987, 23, (1), 229. [CA: 107, 175541g]
[12]
Sulfonate activation of N-chloroamines and sulfenamides by pyridine - sulfur trioxide in reactions with olefins. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Kolbasenko, S.I. Zh. Org. Khim., 1987, 23, (1), 227. [CA: 107, 197597g]
[11]
Electrophilic sulfamatosulfenylation of olefins. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Lapin, Yu.A. Zh. Org. Khim., 1987, 23, (2), 392. [CA: 108, 37306d]
[10]
Structure of 7-(2,4-Dinitrophenylthio)-exo-5-nitrobicyclo[2.2.1]hept-2-exo-yl Acetate. Sergeeva, M.V.; Yufit, D.S.; Struchkov, Yu.T.; Kurkutova, E.N.; Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Kolbasenko, S.I. Acta Crystallogr., , 1986, C42, 1164. [CA: 106, 93941c]
[9]
Crystal and molecular structure of 3-(4-nitrophenylthio)-nortricyclane, C13H13NO2S. Potekhin, K.A.; Lindeman, S.B.; Struchkov, Yu.T.; Zyk, N.V.; Kutateladze, A.G.; Lapin, Yu.A.; Zefirov, N.S. Dokl. Acad. Nauk SSSR , 1986, 292, (4), 873. [CA: 107, 175542h]
[8]
Acid-catalized nucleophilic substitution of the N,N-diethylsulfamate group. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Lapin, Yu.A.; Chizhov, A.O. Zh. Org. Khim., 1986, 22, (11), 2462. [CA: 107, 197570t]
[7]
Crystal and molecular structure of exo-5-(4-nitrophenylthio)-endo-nortricyclene-3-ol N,N-dimethylsulfamate, C15H18N2O5S2. Potekhin, K.A.; Sedov, B.B.; Struchkov, Yu.T.; Zyk, N.V.; Kutateladze, A.G; Lapin, Yu.A.; Zefirov, N.S. Dokl. Acad. Nauk SSSR , 1986, 290, (3), 627. [CA: 107, 39262q]
[6]
New reaction: sulfamatosulfenylation of olefins. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G.; Kolbasenko, S.I.; Lapin, Yu.A. Zh. Org. Chem., 1986, 22, (1), 214. [CA: 106, 17940m]
[5]
Sulfur Trioxide Assisted Electrophilic Addition of R2N-Cl to Olefins. Zefirov, N.S.; Zyk, N.V.; Kolbasenko, S.I.; Kutateladze, A.G. J. Org. Chem., 1985, 50, 4539.
[4]
Sulfur trioxide activation of the addition of ethyl nitrite to olefins. Zefirov, N.S.; Zyk, N.V.; Kutateladze, A.G. Zh. Org. Khim. , 1984, 20, (11), 2473. [CA: 102, 112911d]
[3]
Reaction of chlorosulfamation of olefins. Zefirov, N.S.; Zyk, N.V.; Kolbasenko, S.I.; Kutateladze, A.G. Sulfur Lett. , 1984, 2, (3), 95. [CA: 102, 5740a]
[2]
Conjugate addition of NO2Cl to cycloolefins. Zyk, N.V.; Nikulin, A.V.; Kolbasenko, S.I.; Kutateladze, A.G.; Zefirov, N.S. Zh. Org. Khim. , 1984, 20, (6), 1329. [CA: 102, 24131]
[1]
Reactions of N-chloroamines with olefins in the presence of sulfur trioxide. Zefirov, N.S.; Zyk, N.V.; Kolbasenko, S.I.; Kutateladze, A.G. Izv. Acad. Nauk SSSR, Ser. Khim. , 1984, (4), 959. [CA: 101, 90449j]