Enantioselective Total Syntheses of Trichodermamides A and B

被引：27
|
作者：
Wan, Xiaobo [1 ]
Joullie, Madeleine M. [1 ]
机构：
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
来源：
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2008年 / 130卷 / 51期
关键词：
D O I：
10.1021/ja807011b
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Starting from commercially available (-)-quinic acid, the enantioselective total syntheses of trichodermamides A and B were achieved. The key reactions involve the stereoselective construction of the oxazine ring via an intramolecular epoxide ring opening reaction and an EDCl-assisted peptide coupling reaction,
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页码：17236 / +
页数：3
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