Enantioselective Synthesis of (+)-Cephalostatin 1
2009; American Chemical Society; Volume: 132; Issue: 1 Linguagem: Inglês
10.1021/ja906996c
ISSN1943-2984
AutoresKevin C. Fortner, Darryl Kato, Yoshiki Tanaka, Matthew D. Shair,
Tópico(s)Marine Sponges and Natural Products
ResumoThis Article describes an enantioselective synthesis of cephalostatin 1. Key steps of this synthesis are a unique methyl group selective allylic oxidation, directed C−H hydroxylation of a sterol at C12, Au(I)-catalyzed 5-endo-dig cyclization, and a kinetic spiroketalization.
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