First enantioselective synthesis of tetracyclic intermediates en route to madangamine D.
نویسندگان
چکیده
The enantioselective synthesis of advanced tetracyclic precursors of madangamine D, bearing rings ABCD of this alkaloid, is reported. The saturated 14-membered ring is assembled from functionalized diazatricyclic intermediates following either ring-closing metathesis or macrolactamization strategies.
منابع مشابه
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ورودعنوان ژورنال:
- Chemical communications
دوره 49 30 شماره
صفحات -
تاریخ انتشار 2013