James E. Taylor

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Organization: University of St. Andrews , England
Department: School of Chemistry
Title: Research Fellow(PhD)
Co-reporter:Alison J. Fugard, Bethany K. Thompson, Alexandra M. Z. Slawin, James E. Taylor, and Andrew D. Smith
Organic Letters 2015 Volume 17(Issue 23) pp:5824-5827
Publication Date(Web):November 24, 2015
DOI:10.1021/acs.orglett.5b02997
Hydrazone-carboxylic acids undergo intramolecular cyclization in the presence of pivaloyl chloride, iPr2NEt, and catalytic DABCO to form a range of substituted fused tricyclic 2,3-dihydro-1,3,4-oxadiazoles in high yields.
2-Thiopheneacetic acid, anhydride
Benzeneacetic acid, 4-methyl-, anhydride
D-Alanine, N-phenyl-, methyl ester
Ethanone, 1-(1H-benzotriazol-1-yl)-2-phenyl-
3-Buten-2-ol, 1,1,1-trichloro-4-phenyl-, (3E)-
Oxaziridine, 3-(4-bromophenyl)-2-[(4-methylphenyl)sulfonyl]-
2H-Pyrimido[2,1-b]benzothiazole, 3,4-dihydro-
Ethanone, 2-hydroxy-2-(2-methoxyphenyl)-1-phenyl-
2-Butenoic acid, 4-(4-methoxyphenyl)-, ethyl ester, (2E)-
Tricyclo[3.3.1.13,7]decane, 1,3,5,7-tetrakis(4-ethynylphenyl)-