Andrew Phillips

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Organization: Yale University
Department: Department of Chemistry
Title:
Co-reporter:Michal S. Hallside, Richard S. Brzozowski, William M. Wuest, and Andrew J. Phillips
Organic Letters 2014 Volume 16(Issue 4) pp:1148-1151
Publication Date(Web):January 31, 2014
DOI:10.1021/ol500004k
A synthesis of carolacton, a myxobacterial natural product that has profound effects on Streptococcus mutans biofilms, is reported. The synthesis proceeds via a longest linear sequence of 14 steps from an Evans β-ketoimide and enabled preliminary evaluations of the effects of late-stage intermediates on S. mutans biofilms. These studies suggest that further investigations into carolacton’s structure–function relationships are warranted.
Co-reporter:Jamie McCabe, Andrew J. Phillips
Tetrahedron 2013 69(27–28) pp: 5710-5714
Publication Date(Web):
DOI:10.1016/j.tet.2013.04.105
carolacton
Propanal, 3-[(4-methoxyphenyl)methoxy]-
2-Oxazolidinone, 3-[(2S)-2-methyl-1,3-dioxopentyl]-4-(phenylmethyl)-,(4S)-
pyruvate kinase from rabbit muscle