期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 29, 页码 9968-9969出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja103152k
关键词
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A biomimetic three-step transformation of classical 6-6-6-5-steroids into their C-nor-D-homo-counterparts gives an easy and fast access to this highly important substructure of natural products, as it is found in cyclopamine, and nakiterpiosin. A novel reagent combination allows for the rearrangement even of 17-keto steroids with high endoselectivity. In several examples the broadness of this strategy is outlined.
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