Organic Lettersжурнал

Редколлегия

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• Кузнецов Николай Юрьевич, с 1 ноября 2016

Статьи, опубликованные в журнале стиль:  обычный | ГОСТ | plain | abbrv | acm | alpha | amsalpha | amsplain | apalike | ieeetr | siam

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  • 2020 From Russia, With Chemistry
  • Carreira Erick M., Nenajdenko Valentine G., Miller Scott J., Chirik Paul J., Meyer Karsten
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 22, № 3, с. 765-767 DOI
• • 2020 Imidazol-5-one as an Acceptor in Donor–Acceptor Cyclopropanes: Cycloaddition with Aldehydes
  • Mikhaylov Andrey A., Kuleshov Andrei V., Solyev Pavel N., Korlyukov Alexander A., Dorovatovskii Pavel V., Mineev Konstantin S., Baranov Mikhail S.
  • в журнале Organic Letters, издательство American Chemical Society (United States) DOI
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  • 2020 Reversible Shifting of a Chemical Equilibrium by Light: The Case of Keto–Enol Tautomerism of a $\upbeta$-Ketoester
  • Lvov Andrey G., Yadykov Anton V., Lyssenko Konstantin A., Heinemann Frank W., Shirinian Valerii Z., Khusniyarov Marat M.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 22, № 2, с. 604-609 DOI
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  • 2019 Amination of Aryl Boronic Acids with Alkylnitrites: A Convenient Complement to Cu-Promoted Reductive Amination
  • Levitskiy Oleg A., Magdesieva Tatiana V.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 24, с. 10028-10032 DOI
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  • 2019 Chameleon-Like Activating Nature of the Spirooxindole Group in Donor–Acceptor Cyclopropanes
  • Akaev Andrey A., Melnikov Mikhail Ya, Budynina Ekaterina M.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 23, с. 9795-9799 DOI
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  • 2019 Golden face of phosphine: cascade reaction to bridgehead methanophosphocines by intramolecular double hydroarylation
  • Babouri R., Traore L., Bekro Y.A., Matveeva V.I., Sadykova Yu M., Voronina J.K., Burilov A.R., Ayad T., Volle J.N., Virieux D., Pirat J.L.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 1, с. 45-49 DOI
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  • 2019 Phosphazenomalonates as Catalysts and Reactants in (4+3) Annulation to Acrolein
  • Ivanov Konstantin L., Melnikov Mikhail Ya, Budynina Ekaterina M.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 12, с. 4464-4468 DOI
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  • 2019 Photoswitching off the Antiproliferative Activity of Combretastatin A-4 Analogues
  • Yadykov Anton V., Scherbakov Alexander M., Trofimova Victoria V., Lvov Andrey G., Markosyan Ashot I., Zavarzin Igor V., Shirinian Valerii Z.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 23, с. 9608-9612 DOI
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  • 2019 Sigmatropic Rearrangement-Based Synthesis of 4-Alkenyl-1,3-dithiol-2-ones
  • Ostrovskis Pavels, Mikhaylov Andrey A., Zard Samir Z.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 10, с. 3726-3729 DOI
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  • 2019 Trifluoroacetaldehyde N‑Tosylhydrazone as a Precursor of Trifluorodiazoethane in Reactions of Insertion into the Heteroatom−Hydrogen Bond
  • Ostrovskii Vladimir S., Beletskaya Irina P., Titanyuk Igor D.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 22, с. 9080-9083 DOI
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  • 2019 aza-Wittig Reaction with Nitriles: How Carbonyl Function Switches from Reacting to Activating
  • Tukhtaev Hamidulla B., Ivanov Konstantin L., Bezzubov Stanislav I., Cheshkov Dmitry A., Melnikov Mikhail Ya, Budynina Ekaterina M.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 21, № 4, с. 1087-1092 DOI
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  • 2018 Adducts of triallylborane with ammonia and aliphatic amines as stoichiometric allylating agents for aminoallylation reaction of carbonyl compounds
  • Кузнецов Н.Ю., Тихов Р.М., Стрелкова Т.В., Бубнов Ю.Н.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 12, с. 3549-3552 DOI
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  • 2018 Annulation-Induced Cascade Transformation of 5-Iodo-1,2,3-triazoles to 2-(1-Aminoalkyl)benzoxazoles
  • Kotovshchikov Yury N., Latyshev Gennadij V., Navasardyan Mger A., Erzunov Dmitry A., Beletskaya Irina P., Lukashev Nikolay V.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 15, с. 4467-4470 DOI
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  • 2018 Atom- and Step-Economical Ruthenium-Catalyzed Synthesis of Esters from Aldehydes or Ketones and Carboxylic Acids
  • Runikhina Sofiya A., Usanov Dmitry L., Chizhov Alexander O., Chusov Denis
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 24, с. 7856-7859 DOI
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  • 2018 Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group
  • Ivanova O.A., Andronov V.A., Vasin V.S., Shumsky A.N., Rybakov V.B., Voskressensky L.G., Trushkov I.V.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 24, с. 7947-7952 DOI
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  • 2018 Heck Reaction of Electronically Diverse Tertiary Alkyl Halides
  • Kurandina Daria, Rivas Mónica, Radzhabov Maxim, Gevorgyan Vladimir
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 2, с. 357-360 DOI
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  • 2018 N-Arylation of DABCO with Diaryliodonium Salts: General Synthesis of N-Aryl-DABCO Salts as Precursors for 1,4-Disubstituted Piperazines
  • Bugaenko Dmitry I., Yurovskaya Marina A., Karchava Alexander V.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 20, с. 6389-6393 DOI
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  • 2018 Photocatalytic Reductive Fluoroalkylation of Nitrones
  • Supranovich Vyacheslav I., Levin Vitalij V., Struchkova Marina I., Dilman Alexander D.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 3, с. 840-843 DOI
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  • 2018 Synthesis of Indoles via Electron-Catalyzed Intramolecular C–N Bond Formation
  • Bugaenko Dmitry I., Dubrovina Anastasia A., Yurovskaya Marina A., Karchava Alexander V.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 23, с. 7358-7362 DOI
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  • 2018 Synthesis of a New Family of 1,1-Diazidoethenes: One-Pot Construction of 4-Azido-1,2,3-triazoles via Nitrene Cyclization
  • Shastin Alexey V., Tsyrenova Biligma D., Sergeev Pavel G., Roznyatovsky Vitaly A., Smolyar Ivan V., Khrustalev Victor N., Nenajdenko Valentine G.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 20, № 24, с. 7803-7806 DOI
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  • 2017 Aerobic Dimerization of Ethyl 4‑Thienyl-3-ketobutanoate toward a Modifiable Photochromic Diarylethene Precursor
  • Lvov A.G., Milevsky N.A., Yanina A.M., Kachala V.V., Shirinian V.Z.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 19, № 16, с. 4395-4398 DOI
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  • 2017 Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination
  • Kolesnikov Pavel N., Usanov Dmitry L., Muratov Karim M., Chusov Denis
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 19, № 20, с. 5657-5660
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  • 2017 Difluoromethylation of Carboxylic Acids via the Addition of Difluorinated Phosphorus Ylide to Acyl Chlorides
  • Trifonov Alexey L., Levin Vitalij V., Struchkova Marina I., Dilman Alexander D.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 19, № 19, с. 5304-5307 DOI
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  • 2017 Extension to the Silyl-Tethered Radical Cyclization: Cyclohex-2-en-1-oxy Vinyl Silanes in Stereoselective Radical Addition/Cyclization Cascades
  • Mikhaylov Andrey A., Zard Samir Z.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 19, № 7, с. 1866-1869 DOI
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  • 2017 Protonation-Gated Dual Photochromism of a Chromene–Styryl Dye Hybrid
  • Berdnikova Daria V., Paululat Thomas, Jonusauskas Gediminas, Peregudova Svetlana M., Fedorova Olga A.
  • в журнале Organic Letters, издательство American Chemical Society (United States), том 19, № 20, с. 5633-5636 DOI