Title : ( Mechanism and regioselectivity of 1,3-dipolar cycloaddition reactions of bicyclic monoterpenes with aryl and heteroaryl nitrile oxides: a DFT study )
Authors: Hossein Eshghi , Amir khojastehnezhad golmakani , Farid Moeinpour , Mehdi Bakavoli ,
دانلود فایل برای اعضای دانشگاهAccess to full-text not allowed by authors
Abstract
The reactivity and regioselectivity of 1,3-dipolar cycloaddition reactions of aryl and heteroaryl nitrile oxides (1a–1c) with bicyclic monoterpenes (R)-(+)-a-pinene (2a) and (S)-(–)-b-pinene (2b) have been investigated by using density functional theory based on reactivity indices and activation energy calculations at the B3LYP/6-31G(d) level of theory in the gas phase. The potential energy surface analyses for both reactions are in agreement with the experimental observations. Moreover, our calculations on the geometries, bond orders, and global electron density transfers at the transition state structures shows that these 1,3- dipolar cycloaddition reactions occur via an asynchronous one-step mechanism.
Keywords
, regioselectivity, 1, 3-dipolar cycloaddition, bicyclic monoterpenes, nitrile oxides, DFT.
@article{paperid:1048427,
author = {Eshghi, Hossein and Khojastehnezhad Golmakani, Amir and Farid Moeinpour and Bakavoli, Mehdi},
title = {Mechanism and regioselectivity of 1,3-dipolar cycloaddition reactions of bicyclic monoterpenes with aryl and heteroaryl nitrile oxides: a DFT study},
journal = {Canadian Journal of Chemistry},
year = {2015},
volume = {93},
number = {7},
month = {July},
issn = {0008-4042},
pages = {749--753},
numpages = {4},
keywords = {regioselectivity; 1;3-dipolar cycloaddition; bicyclic monoterpenes; nitrile oxides; DFT.},
}
%0 Journal Article
%T Mechanism and regioselectivity of 1,3-dipolar cycloaddition reactions of bicyclic monoterpenes with aryl and heteroaryl nitrile oxides: a DFT study
%A Eshghi, Hossein
%A Khojastehnezhad Golmakani, Amir
%A Farid Moeinpour
%A Bakavoli, Mehdi
%J Canadian Journal of Chemistry
%@ 0008-4042
%D 2015
