Issue 2, 1987

The decarboxylative route to azomethine ylides. Stereochemistry of 1,3-dipole formation

Abstract

Stereochemical studies of cycloadducts produced from primary and secondary α-amino acids, aldehydes, and N-methylmaleimide indicate they usually arise from stereospecific or highly stereoselective formation of the anti-isomer of an intermediate azomethine ylide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 47-49

The decarboxylative route to azomethine ylides. Stereochemistry of 1,3-dipole formation

R. Grigg, S. Surendrakumar, S. Thianpatanagul and D. Vipond, J. Chem. Soc., Chem. Commun., 1987, 47 DOI: 10.1039/C39870000047

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