1,3-Dipolar cycloaddition reactions of imines of α-amino-acid esters: X-ray crystal and molecular structure of methyl 4-(2-furyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo[3.3.0]octane-2-carboxylate

Abstract
Imines of α-amino acid esters undergo a wide range of cycloadditions probably via their 1,3-dipolar tautomers and the stereochemistry of one adduct has been determined by X-ray crystallography.

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