Computational Study on the Aminolysis of β-Hydroxy-α,β-Unsaturated Ester via the Favorable Path Including the Formation of α-Oxo Ketene Intermediate-Reference-Cited by-同舟云学术

Computational Study on the Aminolysis of β-Hydroxy-α,β-Unsaturated Ester via the Favorable Path Including the Formation of α-Oxo Ketene Intermediate

Published:2008-04-11 Issue:19 Volume:112 Page:4501-4510
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Jin Lu¹,Xue Ying¹,Zhang Hui¹,Kim Chan Kyung¹,Xie Dai Qian¹,Yan Guo Sen¹

Affiliation:

1. College of Chemistry, Sichuan University, Chengdu 610064, P. R. China, State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, P. R. China, Department of Chemistry, Inha University, Incheon 402-751, Korea and Institute of Theoretical and Computational Chemistry, Key Laboratory of Mesoscopic Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp0756496

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3. Effect of Acyl Substituents on the Reaction Mechanism for Aminolyses of 4-Nitrophenyl X-Substituted Benzoates

4. Kinetics and mechanism of the aminolysis of 4-nitrophenyl and 2,4-dinitrophenyl 4-methylphenyl carbonates in aqueous ethanol

5. Effect of Amine Nature on Reaction Mechanism: Aminolyses of O-4-Nitrophenyl Thionobenzoate with Primary and Secondary Amines

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