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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 291–293
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002004 (Mi mendc3915) 		 
This article is cited in 3 scientific papers (total in 3 papers)

Total synthesis of trioxilins 11,12-threo-(8,11,12)-A3 through type B3 trioxilins

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 (139 kB) Citations (3)
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002004
Abstract: 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.
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Document Type: Article
Language: English


Citation: 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
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  • https://www.mathnet.ru/eng/mendc/v14/i6/p291
    • This publication is cited in the following 3 articles:
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