화학공학소재연구정보센터
Journal of the American Chemical Society, Vol.130, No.51, 17236-17236, 2008
Enantioselective Total Syntheses of Trichodermamides A and B
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,