Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products.
نویسندگان
چکیده
An asymmetric synthetic strategy for constructing the divergent-synthesis monomer of epidithiodiketopiperazine (ETP) natural products has been successfully developed. The functionalized 2,3,3a,4,7,7a-hexahydroindole scaffold was constructed by a diastereoselective inverse electron-demand Diels-Alder (IEDDA) reaction.
منابع مشابه
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ورودعنوان ژورنال:
- Chemical communications
دوره 50 68 شماره
صفحات -
تاریخ انتشار 2014