Аннотация:
The total synthesis of trioxilins 11,12-threo-TrXB3 has been extended to the corresponding trioxilins of the (8,11,12)-A3 type. The synthesis involves the allylic rearrangement of a protected TrXB3 derivative with a free 10-hydroxyl group under the Mitsunobu reaction conditions as the key step.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Total synthesis of trioxilins 11,12-threo-(8,11,12)-A3 through type B3 trioxilins”, Mendeleev Commun., 14:6 (2004), 291–293
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3915
https://www.mathnet.ru/rus/mendc/v14/i6/p291
Эта публикация цитируется в следующих 3 статьяx:
Min‐Ju Seo, Tae‐Eui Lee, Soo‐Jin Yeom, Deok‐Kun Oh, Kyung‐Chul Shin, “Biotransformation of Polyunsaturated Fatty Acids to Trioxilins by Lipoxygenase from Pleurotus sajor‐caju”, ChemBioChem, 24:23 (2023)
K. C. Kumara Swamy, N. N. Bhuvan Kumar, E. Balaraman, K. V. P. Pavan Kumar, “Mitsunobu and Related Reactions: Advances and Applications”, Chem. Rev., 109:6 (2009), 2551
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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