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Asymmetric Oxidation of 4-Nitro-6-trifluoromethyl-1,2,3-benzotrithiole Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2009, Volume: 45, Number: 9, Pages: 1402-1404 Pages count : 3 DOI: 10.1134/S1070428009090140
Authors Khomenko T.M. 1 , Korchagina D.V. 1 , Volcho K.P. 1 , Salakhutdinov N.F. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Both enantiomers of 4-nitro-6-trifluoromethyl-1,2,3-benzotrithiole 1-oxide as analogs of Varacins B and C were synthesized for the first time. The use of the Modena method ensures higher optical purity but lower yields of the chiral sulfoxides, as compared to the Kagan procedure.
Cite: Khomenko T.M. , Korchagina D.V. , Volcho K.P. , Salakhutdinov N.F.
Asymmetric Oxidation of 4-Nitro-6-trifluoromethyl-1,2,3-benzotrithiole
Russian Journal of Organic Chemistry. 2009. V.45. N9. P.1402-1404. DOI: 10.1134/S1070428009090140 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Sep 1, 2009
Published online: Oct 13, 2009
Identifiers:
Web of science: WOS:000270744600014
Scopus: 2-s2.0-70350004101
Elibrary: 15296906
OpenAlex: W2017929272
Citing:
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Web of science 2
Scopus 3
Elibrary 2
OpenAlex 4
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