期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 51, 页码 17236-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja807011b
关键词
-
资金
- NSF [CHEM-0515443]
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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