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Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2016, Volume: 52, Number: 6, Pages: 772-776 Pages count : 5 DOI: 10.1134/S1070428016060026
Authors Ivanova N.I. 1 , Volkov P.A. 1 , Khrapova K.O. 1 , Larina L.I. 1 , Bagryanskaya I.Yu. 2,3 , Gusarova N.K. 1 , Trofimov B.A. 1
Affiliations
1 Favorskii Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia
2 Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, pr. Akademika Lavrent’eva 9, Novosibirsk, 630090, Russia
3 Novosibirsk State University, ul. Pirogova 2, Novosibirsk, 630090, Russia

Abstract: Aryl(diarylphosphoryl)methanols reacted with alkyl propiolates under mild conditions (triethylamine, THF, 22aEuro'25A degrees C), to give the corresponding anti-Markovnikov adducts, alkyl (E)-3-[aryl(diarylphosphoryl) methoxy]prop-2-enoates, with high yields (84-90%) and regio- and stereoselectivity.
Cite: Ivanova N.I. , Volkov P.A. , Khrapova K.O. , Larina L.I. , Bagryanskaya I.Y. , Gusarova N.K. , Trofimov B.A.
Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers
Russian Journal of Organic Chemistry. 2016. V.52. N6. P.772-776. DOI: 10.1134/S1070428016060026 WOS Scopus РИНЦ OpenAlex
Original: Иванова Н.И. , Волков П.А. , Храпова К.О. , Ларина Л.И. , Багрянская И.Ю. , Гусарова Н.К. , Трофимов Б.А.
Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
Журнал органической химии (RUSS J ORG CHEM+). 2016. Т.52. №6. С.788-792. РИНЦ
Dates:
Published print: Jun 1, 2016
Published online: Jul 24, 2016
Identifiers:
Web of science: WOS:000380211600002
Scopus: 2-s2.0-84979302769
Elibrary: 27094755
OpenAlex: W2495710232
Citing:
DB Citing
Web of science 5
Scopus 5
Elibrary 4
OpenAlex 4
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