M. A. Lapitskaya, L. L. Vasiljeva, G. V. Zatonsky, K. K. Pivnitsky, “Synthesis of series 2 trioxilins from trioxilin B<sub>3</sub> by selective hydrogenation”, Mendeleev Commun., 2000, Volume 10, Issue 4,Pages <nobr>130

This article is cited 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

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.

Language: English

DOI: 10.1070/MC2000v010n04ABEH001297