| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286985 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Xestobergsterol A, a potent inhibitor of histamine release, has been synthesized from dehydroepiandrosterone in a route that used introduction of a novel 15-oxygen functionality, side-chain construction via the orthoester Claisen rearrangement and TBAF-promoted epimerization-aldol condensation.
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Physical Sciences and Engineering
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Organic Chemistry
Authors
Atsuko Nakamura, Yuko Kaji, Kana Saida, Michiko Ito, Yumi Nagatoshi, Noriyuki Hara, Yoshinori Fujimoto,