Literature DB >> 18758615

Remote induction of asymmetry in [13]-macro-dilactone topology by a single stereogenic center.

W Sean Fyvie1, Mark W Peczuh.   

Abstract

Analysis of a series of unsaturated [13]-macro-dilactones showed that the configuration of a single carbon dictates the planar chirality of a macrocycle backbone and in turn remotely switches the facial display of an embedded alkene unit.

Entities:  

Year:  2008        PMID: 18758615     DOI: 10.1039/b807562j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Synthesis and evaluation of antimigratory and antiproliferative activities of lipid-linked [13]-macro-dilactones.

Authors:  Anniefer N Magpusao; Richard T Desmond; Katelyn J Billings; Gabriel Fenteany; Mark W Peczuh
Journal:  Bioorg Med Chem Lett       Date:  2010-07-25       Impact factor: 2.823

2.  De novo macrolide-glycolipid macrolactone hybrids: Synthesis, structure and antibiotic activity of carbohydrate-fused macrocycles.

Authors:  Richard T Desmond; Anniefer N Magpusao; Chris Lorenc; Jeremy B Alverson; Nigel Priestley; Mark W Peczuh
Journal:  Beilstein J Org Chem       Date:  2014-09-17       Impact factor: 2.883

  2 in total

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