Asymmetric Total Synthesis of (+)-Strychnine

Strychnos Chirality
DOI: 10.1021/acs.orglett.8b03686 Publication Date: 2018-12-18T13:07:13Z
ABSTRACT
A synthetic strategy for the catalytic asymmetric total synthesis of (+)-strychnine is disclosed. Key features this include an organocatalytic enantioselective Michael addition to establish chirality starting building block, a photoinduced radical cascade reaction access Corynanthe alkaloid intermediate, and bioinspired rearrangement generate core Strychnos alkaloids.
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