| Literature DB >> 31188001 |
Taku Imaizumi1, Yumi Yamashita1, Yuki Nakazawa1, Kentaro Okano1, Juri Sakata1, Hidetoshi Tokuyama1.
Abstract
An indole synthesis via ring expansion of benzocyclobutenone oxime sulfonate was developed. Utility of the indole synthesis was demonstrated by the total synthesis of (+)-CC-1065. The middle and right segments were constructed by a sequential ring expansion of the symmetrical benzo-bis-cyclobutenone. The left segment was also constructed via ring expansion of the methyl-substituted benzocyclobutenone oxime sulfonates. After condensation of these three segments, the dienone cyclopropane structure was formed to complete the total synthesis.Entities:
Year: 2019 PMID: 31188001 DOI: 10.1021/acs.orglett.9b01690
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005