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A DFT‐based exploration augmented by X‐ray and NMR of the stereoselectivity in the 1,3‐dipolar cycloaddition of 1‐pyrroline‐1‐oxide to methyl cinnamate and benzylidene acetophenone
Author(s) -
Acharjee Nivedita,
Das Tapas Kumar,
Banerji Avijit,
Banerjee Manas,
Prangé Theirry
Publication year - 2010
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.1690
Subject(s) - chemistry , cycloaddition , acetophenone , regioselectivity , electrophile , stereoselectivity , pyrroline , stereochemistry , reactivity (psychology) , 1,3 dipolar cycloaddition , carbon 13 nmr , adduct , computational chemistry , medicinal chemistry , organic chemistry , catalysis , alternative medicine , pathology , medicine
A B3LYP/6–31G* study was carried out for the reactions of 1‐pyrroline‐1‐oxide (N1) with methyl cinnamate (E1) and benzylidene acetophenone (E2) for getting a quantitative rationalization of the experimental findings. The product ratios were determined by NMR studies of the crude reaction mixtures. The conformation and stereochemistry of the isolated cycloadducts were finally confirmed by 2D NMR and X‐ray diffraction. The endo/exo‐ selectivities were predicted through the computation of activation parameters on the basis of assumed concerted mechanism. The regioselectivity and reactivity were amply predicted by local and global electrophilicity indices and were found to be in good agreement with the experimental findings which were supportive of polar character and of the direction of charge transfer (CT) accompanying the cycloaddition. It was found that the cycloaddition involving methyl cinnamate was endo‐ selective, while that with benzylidene acetophenone produced the exo‐ isomer as the major adduct. Copyright © 2010 John Wiley & Sons, Ltd.