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THEORETICAL STUDY ON THE TAUTOMERE l-N-BENZYL-4-SUBSTITUTED-PHENACYL MONOSUBSTITUTED CARBANION CYCLOIMMONIUM YLIDES


MIRON DORU NECULAI*, SURPATEANU GHEORGHE**, MARDARE IRINEL*, DRON PAUL IONUŢ*
*LABORATORY OF ORGANIC SYNTHESIS AND STRUCTURAL ANALYSIS, UNIVERSITY OF BACÄ‚U; **LABORATORY OF ORGANIC SYNTHESIS AND ENVIRONMENT, UNIVERSITY OF LITTORAL DUNKERQUE, FRANCE

Issue:

SCSCC6, Volume II

Section:

Volume II (2001)

Abstract:

The work presents the theoretical study on the reactivity of the benzyl-phenacyl monosubstituted benzotriazolium ylides. As theoretical methods for investigation we used the MM3 method (for molecular mechanics), AMI and PM3 (semi empirical methods for quantic mechanics). In order to modelate the process we considered the diphenacyl-benzotriazolium ylides and we evaluated their reactivity.

Keywords:

benzyl-phenacyl-benzotriazolium ylides, carbanion disubstituted cycloimmonium ylides, semi empirical methods for quantic mechanics, molecular mechanics.

Code [ID]:

CSCC6200102V00S01A0005 [0001333]

Full paper:

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