| Literature DB >> 11674153 |
Susan V. Downing1, Enrique Aguilar, A. I. Meyers.
Abstract
The total synthesis of the macrocyclic hexapeptide bistratamide D is reported. The synthetic strategy involved assembly of enantiomerically pure oxazole, thiazole, and oxazoline segments derived from amino acids. Macrocyclization of the hexapeptidic aminooxazoline-oxazole-thiazole carboxylic acid fragment was accomplished by activation with O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HATU).Entities:
Year: 1999 PMID: 11674153 DOI: 10.1021/jo981664i
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354