| Literature DB >> 11558613 |
T Yoshida1, A Ito, K Ibusuki, M Murase, E Kotani.
Abstract
Sulfur substituted 3-vinylpyrrole 10 was prepared from 3-thio-acetylpyrrole 9 by alkylation with alkyl halide in the presence of propylene oxide. Functionalized 4-alkylthioindoles were made by Diels-Alder reaction of the 3-vinylpyrrole 10 with dienophiles. Chuangxinmycin analogues were synthesized by using some of the functionalized 4-alkylthioindoles as key intermediates.Entities:
Mesh:
Substances:
Year: 2001 PMID: 11558613 DOI: 10.1248/cpb.49.1198
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645