Issue 3, 1978
From the journal:

Journal of the Chemical Society, Chemical Communications

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

Ronald Grigg,   James Kemp,   George Sheldrick  and  Jill Trotter  

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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Article information

DOI
https://doi.org/10.1039/C39780000109
Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 109-111

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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

R. Grigg, J. Kemp, G. Sheldrick and J. Trotter, J. Chem. Soc., Chem. Commun., 1978, 109 DOI: 10.1039/C39780000109

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