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埃兰索利德B1和B2的全合成。

Total synthesis of elansolids B1 and B2.

作者信息

Wang Liang-Liang, Kirschning Andreas

机构信息

Institute of Organic Chemistry and Center of Biomolecular Drug Research (BMWZ), Leibniz University Hannover, Schneiderberg 1b, 30167 Hannover, Germany.

出版信息

Beilstein J Org Chem. 2017 Jun 28;13:1280-1287. doi: 10.3762/bjoc.13.124. eCollection 2017.

Abstract

The elansolids A1-A3, B1, and B2 are secondary metabolites formed by the gliding bacterium . They show antibacterial activity against Gram-positive bacteria. A second generation total synthesis of the antibiotic elansolid B1 () and the first synthesis of elansolid B2 () are reported. In contrast to previous work, the (-triene at C10-C15 was assembled by using an optimized C-C cross-coupling sequence with a Suzuki cross-coupling reaction as key step.

摘要

伊兰索利德A1 - A3、B1和B2是由滑行细菌形成的次生代谢产物。它们对革兰氏阳性菌具有抗菌活性。本文报道了抗生素伊兰索利德B1()的第二代全合成以及伊兰索利德B2()的首次合成。与之前的工作不同,C10 - C15处的(-三烯是通过使用以铃木交叉偶联反应为关键步骤的优化碳 - 碳交叉偶联序列构建而成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd48/5496564/20023cd1ff16/Beilstein_J_Org_Chem-13-1280-g002.jpg

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