|
Эта публикация цитируется в 4 научных статьях (всего в 4 статьях)
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
Аннотация:
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.
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3914 https://www.mathnet.ru/rus/mendc/v14/i6/p287
|
|
Обратная связь: