Computational studies of the effects of ortho-ring and para-ring activation on the kinetics of SN Ar reactions of 1-chloro-2-nitrobenzene and 1-phenoxy-2-nitrobenzene with aniline-Reference-Cited by-同舟云学术

Computational studies of the effects of ortho-ring and para-ring activation on the kinetics of SN Ar reactions of 1-chloro-2-nitrobenzene and 1-phenoxy-2-nitrobenzene with aniline

Published:2014-12-22 Issue:1 Volume:28 Page:57-67
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Oloba-Whenu Oluwakemi A.¹,Isanbor Chukwuemeka¹

Affiliation:

1. Chemistry Department; University of Lagos; Lagos Nigeria

Funder

Central Research Committee Mini Grant, University of Lagos, Nigeria

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3400/fullpdf

Reference46 articles.

1. Rationalizing the Regioselectivity in Polynitroarene Anionic .sigma.-Adduct Formation. Relevance to Nucleophilic Aromatic Substitution

2. Recent Advances in Diaryl Ether Synthesis

3. Synthesis of Diaryl Ethers, Diaryl Thioethers, and Diarylamines Mediated by Potassium Fluoride−Alumina and 18-Crown-6: Expansion of Scope and Utility1

4. Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6

5. Modern Nucleophilic Aromatic Substitution

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