Daniel R. Nicponski

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Organization: Purdue University
Department: Department of Chemistry
Title:
Co-reporter:Daniel R. Nicponski
Tetrahedron Letters 2014 Volume 55(Issue 13) pp:2075-2077
Publication Date(Web):26 March 2014
DOI:10.1016/j.tetlet.2014.02.024
The catalytic action of 4-(dimethylamino)pyridine (DMAP) in lactonizing 4-hydroxy-2-methylenebutanoate esters to 2-methylene-γ-butyrolactones is described. The use of DMAP, which functions as an excellent complement to the more traditional acid-catalyzed lactonization protocol, allows for the synthesis of 2-methylene-γ-butyrolactones containing acid-sensitive groups under essentially neutral conditions.
2-CYCLOHEXEN-1-ONE, 3-[2-(PHENYLTHIO)ETHYL]-
PHOSPHINE OXIDE, DIPHENYL[2-(PHENYLTHIO)-2-PROPENYL]-
Cyclopentanone, 3,3'-[1,2-ethanediylbis(thio)]bis-
Propanoic acid, 3-(phenylthio)-, 1,1-dimethylethyl ester
Cyclopentanone, 3-[(4-methoxyphenyl)thio]-
2-Propenoic acid, 2-(bromomethyl)-3-(4-methylphenyl)-, methyl ester, (2Z)-
Methyl 2-(hydroxy(p-tolyl)methyl)acrylate
Methyl 2-(bromomethyl)-3-phenylprop-2-enoate