Literature DB >> 11674153

Total Synthesis of Bistratamide D.

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


  2 in total

1.  Sulfur(iv)-mediated umpolung α-heterofunctionalization of 2-oxazolines.

Authors:  Qifeng Zhang; Yuchen Liang; Ruiqi Li; Ziyi Huang; Lichun Kong; Peng Du; Bo Peng
Journal:  Chem Sci       Date:  2022-04-09       Impact factor: 9.969

2.  An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center.

Authors:  Chi-Ming Cheung; Frederick W Goldberg; Philip Magnus; Claire J Russell; Rachel Turnbull; Vince Lynch
Journal:  J Am Chem Soc       Date:  2007-09-19       Impact factor: 15.419

  2 in total

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