| Literature DB >> 18618900 |
Zhen-Hua Ma1, Ni Song, Chun-Xia Li, Wei Zhang, Peng Wang, Ying-Xia Li.
Abstract
The total synthesis of a marine acyclic peptide tasiamide and three diastereomers was reported for the first time. The synthesis has led to a reassignment of the N(alpha)-Me-L-Gln of tasiamide to be N(alpha)-Me-D-Gln, which was supported by 1H NMR, 13C NMR, COSY, HMQC, HMBC, and optical rotation. Copyright 2008 European Peptide Society and John Wiley & Sons, Ltd.Entities:
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Year: 2008 PMID： 18618900 DOI： 10.1002/psc.1051
Source DB: PubMed Journal: J Pept Sci ISSN： 1075-2617 Impact factor: 1.905