Issue 3, 1998
From the journal:

Chemical Communications

Stereoselective intramolecular aldol reactions of (4R)-3-(3-oxobutanoyl)-1,3-thiazolidine-4-carboxylates believed to be directed by ‘self-induced’ axial chirality

Andrew G. Brewster,   Christopher S. Frampton,   Mark B. Mitchell,   Jay Jayatissa,   Richard J. Stoodley  and  Shaheen Vohra  

Abstract

Essentially complete retention of configuration accompanies the base-induced aldol reaction of the thiazolidinecarboxylate 6c to give the fused heterocycles 7c and 8c and their retroaldol–acylation reactions to give the bicycle 9c.

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Article information

DOI
https://doi.org/10.1039/A707388G
Article type
Paper

Chem. Commun., 1998, 299-300

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Stereoselective intramolecular aldol reactions of (4R)-3-(3-oxobutanoyl)-1,3-thiazolidine-4-carboxylates believed to be directed by ‘self-induced’ axial chirality

A. G. Brewster, C. S. Frampton, M. B. Mitchell, J. Jayatissa, R. J. Stoodley and S. Vohra, Chem. Commun., 1998, 299 DOI: 10.1039/A707388G

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