Enantioselective total syntheses of trichodermamides A and B.
نویسندگان
چکیده
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 EDCI-assisted peptide coupling reaction.
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عنوان ژورنال:
- Journal of the American Chemical Society
دوره 130 51 شماره
صفحات -
تاریخ انتشار 2008