Issue 6, 1972

2,3-Sigmatropic rearrangement of nucleophilic carbenes. A new approach to stereospecific synthesis of carbon–carbon bonds

Abstract

S-Methyl-S-(3,3-dimethylallyl)carbene, generated by Bamford–Stevens reaction of the corresponding toluene-p-sulphonylhydrazone, undergoes a 2,3-sigmatropic rearrangement to a dithiocarboxylic acid ester, thereby providing a new carbon–carbon bond synthesis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 354-355

2,3-Sigmatropic rearrangement of nucleophilic carbenes. A new approach to stereospecific synthesis of carbon–carbon bonds

J. E. Baldwin and J. A. Walker, J. Chem. Soc., Chem. Commun., 1972, 354 DOI: 10.1039/C39720000354

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