Total synthesis of N-methylsansalvamide A was accomplished in solution phase by a convergent approach. An N-Boc-td-depsipepide 6 and a dipeptide ester 10 were prepared in the yield of 89% and 91%, respectively. Cycliz...Total synthesis of N-methylsansalvamide A was accomplished in solution phase by a convergent approach. An N-Boc-td-depsipepide 6 and a dipeptide ester 10 were prepared in the yield of 89% and 91%, respectively. Cyclization of the linear penta-depsipetide was achieved with PyBOP and DIPEA in DMF-CH2C12.展开更多
基金The authors are grateful to The National Natural Science Foundation of China （No.30472074） to The Hebei province Natural Science Foundation （No.B2006000302） for financial support of this work.
文摘Total synthesis of N-methylsansalvamide A was accomplished in solution phase by a convergent approach. An N-Boc-td-depsipepide 6 and a dipeptide ester 10 were prepared in the yield of 89% and 91%, respectively. Cyclization of the linear penta-depsipetide was achieved with PyBOP and DIPEA in DMF-CH2C12.
