Issue 21, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

A novel highly diastereoselective synthesis of chiral dihydrothiophenes from mesoionic compounds

Martín Avalos,   Reyes Babiano,   Andrés Cabanillas,   Pedro Cintas,   María J. Diánez,   María D. Estrada,   José L. Jiménez,   Amparo López-Castro,   Juan C. Palacios  and  Simeón P. Garrido  

Abstract

Thioisomünchnones undergo 1,3-dipolar cycloaddition with chiral nitroalkenes to afford stereoselectively 4,5-dihydrothiophenes by means of an unprecedented fragmentation of cycloadducts; the structures of these products have been established by single crystal X-ray structure analyses.

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Article information

DOI
https://doi.org/10.1039/C39950002213
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2213-2214

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A novel highly diastereoselective synthesis of chiral dihydrothiophenes from mesoionic compounds

M. Avalos, R. Babiano, A. Cabanillas, P. Cintas, M. J. Diánez, M. D. Estrada, J. L. Jiménez, A. López-Castro, J. C. Palacios and S. P. Garrido, J. Chem. Soc., Chem. Commun., 1995, 2213 DOI: 10.1039/C39950002213

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