Synthesis and structural reconfirmation of bacillamide B
文献类型:期刊论文
作者 | Sun, Xue; Liu, Yi; Liu, Jun; Gu, Guofeng; Du, Yuguo |
刊名 | ORGANIC & BIOMOLECULAR CHEMISTRY
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出版日期 | 2015 |
卷号 | 13期号:14页码:4271-4277 |
英文摘要 | A concise total synthesis of the natural product bacillamide B was accomplished in 30% overall yield starting from L-cystine. The key step was a one-pot four-step process of thiazoline formation via a cascade disulfide cleavage/thiocarbonylation/Staudinger reduction/aza-Wittig reaction using beta-azido disulfide and carboxylic acid as substrates. The absolute configuration of the natural bacillamide B was reconfirmed to be S and the specific optical rotation was revised to (-). |
研究领域[WOS] | Chemistry, Organic |
WOS记录号 | WOS:000351618000022 |
公开日期 | 2016-03-15 |
源URL | [http://ir.rcees.ac.cn/handle/311016/32677] ![]() |
专题 | 生态环境研究中心_环境化学与生态毒理学国家重点实验室 |
推荐引用方式 GB/T 7714 | Sun, Xue,Liu, Yi,Liu, Jun,et al. Synthesis and structural reconfirmation of bacillamide B[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2015,13(14):4271-4277. |
APA | Sun, Xue,Liu, Yi,Liu, Jun,Gu, Guofeng,&Du, Yuguo.(2015).Synthesis and structural reconfirmation of bacillamide B.ORGANIC & BIOMOLECULAR CHEMISTRY,13(14),4271-4277. |
MLA | Sun, Xue,et al."Synthesis and structural reconfirmation of bacillamide B".ORGANIC & BIOMOLECULAR CHEMISTRY 13.14(2015):4271-4277. |
入库方式: OAI收割
来源:生态环境研究中心
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