M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Enantiodivergent total synthesis of trioxilins B3 using Sharpless asymmetric olefin dihydroxylation”, Mendeleev Commun., 14:6 (2004), 287

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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 287–290
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002003 (Mi mendc3914)

This article is cited in 4 scientific papers (total in 4 papers)

Enantiodivergent total synthesis of trioxilins B₃ using Sharpless asymmetric olefin dihydroxylation

M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (258 kB) Citations (4)

DOI: https://doi.org/10.1070/MC2004v014n06ABEH002003

Abstract: The unknown 11,12-threo-stereoisomers of B-type trioxilins, (10R, 11R, 12S)-TrXB3, its (10S)-epimer and their enantiomers were synthesized (as methyl esters) from a common racemic precursor, viz., methyl rac-10-hydroxyeicos-11(E)-ene-5,8,14-triynoate, by Sharpless enantiodirected dihydroxylation of the double bond as the key step.

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Document Type: Article

Language: English

Citation: M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Enantiodivergent total synthesis of trioxilins B₃ using Sharpless asymmetric olefin dihydroxylation”, Mendeleev Commun., 14:6 (2004), 287–290

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https://www.mathnet.ru/eng/mendc/v14/i6/p287

This publication is cited in the following 4 articles:

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