An analysis of reactant approach in concerted 1,3-dipolar cycloadditions by the second moment of localized orbitals
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference17 articles.
1. 1,3-Dipolar cycloadditions. 76. Concerted nature of 1,3-dipolar cycloadditions and the question of diradical intermediates
2. The diradical mechanism for 1,3-dipolar cycloadditions and related thermal pericyclic reactions
3. Reaction of acetylene with fulminic acid. The prototype 1,3-dipolar cycloaddition
4. Theoretical ab initio study of 1,3-dipolar cycloaddition of fulminic acid to acetylene. Support for Firestone's mechanism
5. A statistical analysis of the theoretical results obtained for concerted 1,3-dipolar cycloaddition
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1. Regioselectivity of 1,3-dipolar cycloadditions between aryl azides and an electron-deficient alkyne through DFT reactivity descriptors;Research on Chemical Intermediates;2016-07-19
2. A theoretical approach to the regioselectivity in 1,3-dipolar cycloadditions of diazoalkanes, hydrazoic acid and nitrous oxide to acetylenes, phosphaalkynes and cyanides;Journal of Physical Organic Chemistry;2003-09
3. Use of Local Softness for the Interpretation of Reaction Mechanisms;International Journal of Molecular Sciences;2002-04-25
4. Nitrous Oxide as a 1,3-Dipole: A Theoretical Study of Its Cycloaddition Mechanism;The Journal of Organic Chemistry;2001-08-16
5. 1,3-Dipolar cycloadditions of thionitroso compounds (R–NS): a density functional theory study;Journal of the Chemical Society, Perkin Transactions 2;1999
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