Synthesis and revision of stereochemistry of rubescensin S.
نویسندگان
چکیده
An effective two step transformation of oridonin to 15,16-seco-ent-kaurane skeleton is reported. We also achieved the conversion of one intermediate to natural product rubescensin S and revised its structure as a 13S configuration although 13R is reported in the literature.
منابع مشابه
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ورودعنوان ژورنال:
- Organic & biomolecular chemistry
دوره 9 12 شماره
صفحات -
تاریخ انتشار 2011