Issue 5, 1992

α,β-Unsaturated thiocarbonyl S-sulfides (thiosulfines). Their generation, intramolecular trapping by a non-activated C[double bond, length half m-dash]C dipolarophile via[5 + 2] cycloaddition and trans-sulfurization ability

Abstract

α,β-Unsaturated thiocarbonyl S-sulfides (thiosulfines)10 were generated by sulfurization of the thioketones 5 and were intramolecularly trapped as 1,5-dipoles giving 8, whereas, in the presence of Et3N, they were transformed by trans-sulfurization via 1,5 cyclization into the thioketones 13 capable of undergoing the intramolecular hetero-Diels–Alder reaction to give cycloadducts 9.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 411-413

α,β-Unsaturated thiocarbonyl S-sulfides (thiosulfines). Their generation, intramolecular trapping by a non-activated C[double bond, length half m-dash]C dipolarophile via[5 + 2] cycloaddition and trans-sulfurization ability

T. Saito, M. Nagashima, T. Karakasa and S. Motoki, J. Chem. Soc., Chem. Commun., 1992, 411 DOI: 10.1039/C39920000411

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