Tetrahedron

Aminolyse de carbamates cycliques analogues de la carboxybiotine; catalyse métallique et modélisation de transfert de carboxyle

JM Botella, A Klaebe, J Perie, E Monnier

Index: Botella; Klaebe; Perie; Monnier Tetrahedron, 1992 , vol. 48, # 24 p. 5111 - 5122

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Citation Number: 3

Abstract

Résumé Aminolysis of carbamic esters, a model of the intermediate carboxybiotin in enzymatic carboxylations was studied in organic medium in the presence of a divalent cation. This study establishes electrostatic catalysis of aminolysis, the rate determining step of which is the collapse of the tetrahedral intermediate principally by carbon nitrogen bond breacking. The results also account for the role of the divalent cation present in the ...