Synthetic Studies on Thiostrepton Family of Peptide Antibiotics: Synthesis of the Tetrasubstituted Dihydroquinoline Portion of Siomycin D1
作者:Kimiko Hashimoto、Syuhei Higashibayashi、Tomonori Mori、Kazuyuki Shinko、Masaya Nakata
DOI:10.3987/com-01-9375
日期:——
The tetrasubstituted dihydroquinoline portion of siomycin D 1 , a member of the thiostrepton family of peptide antibiotics, was synthesized from 5,6,7,8-tetrahydroquinoline featuring the modified Reissert-Henze reaction, the homolytic aromatic substitution reaction, the modified Boekelheide rearrangement, and the Jacobsen asymmetric epoxidation.
由 5,6,7,8-四氢喹啉合成了 5,6,7,8-四氢喹啉,其特征是修饰的 Reissert-Henze 反应、均裂芳香族取代反应、修饰的 Boekelheide 重排、和 Jacobsen 不对称环氧化。