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Mendeleev Communications, 2000, Volume 10, Issue 4, Pages 130–131
DOI: https://doi.org/10.1070/MC2000v010n04ABEH001297 (Mi mendc4420) 		 
This article is cited in 3 scientific papers (total in 3 papers)

Synthesis of series 2 trioxilins from trioxilin B3 by selective hydrogenation

M. A. Lapitskaya, L. L. Vasiljeva, G. V. Zatonsky, K. K. Pivnitsky

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (115 kB) Citations (3)
DOI: https://doi.org/10.1070/MC2000v010n04ABEH001297
Abstract: Trioxilins (as methyl esters) (10S,11S,12S)-TrXB2 and its (8E)-isomer were obtained by selective hydrogenation of the 5,6-double bond in (10S,11S,12S)-TrXB3 11,12-acetonide followed by deprotection.
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Document Type: Article
Language: English


Citation: M. A. Lapitskaya, L. L. Vasiljeva, G. V. Zatonsky, K. K. Pivnitsky, “Synthesis of series 2 trioxilins from trioxilin B3 by selective hydrogenation”, Mendeleev Commun., 10:4 (2000), 130–131
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  • https://www.mathnet.ru/eng/mendc/v10/i4/p130
    • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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