Synlett 2019; 30(05): 577-580
DOI: 10.1055/s-0037-1611727
letter
© Georg Thieme Verlag Stuttgart · New York

Synthesis of the C1–C17 Segment of Bafilomycin N

Haruka Sato
,
Seijiro Hosokawa*
Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku-ku, Tokyo 169-8555, Japan   eMail: seijiro@waseda.jp
› Institutsangaben
We are grateful for the financial support from the Sumitomo Foundation and the Tokyo Biochemical Research Foundation. This work was also supported by Grant-in-Aid for Scientific Research on Innovative Areas ‘Frontier Research on Chemical Communications’ (Grant no. 18H04632).
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Publikationsverlauf

Received: 21. Dezember 2018

Accepted after revision: 21. Januar 2019

Publikationsdatum:
21. Februar 2019 (online)


Abstract

The C1–C17 segment of bafilomycin N has been synthesized. The C1–C11 segment was synthesized by the anti-selective vinylogous Mukaiyama aldol reaction with a chiral vinylketene silyl N,O-acetal and the Horner–Wadsworth–Emmons reaction, whereas C12–C17 was constructed by the syn-selective vinylogous Mukaiyama aldol reaction and the Jung’s semipinacol rearrangement. Those segments were connected by the Stille coupling to afford the C1–C17 segment.

Supporting Information