Peptide aldehydes are of great interest as enzyme inhibitors and as starting materials for further chemistry. The solid phase synthesis of such entities is presented through three different approaches: a Weinreb amide linker, a phenyl ester linker, which both can be reduced with hydrides to yield the target molecules, and finally an unsaturated linker which produces the desired compounds by ozonolysis. (C) 1999 Elsevier Science B.V. All rights reserved.
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
Yao, W
Xu, HY
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机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China