Aminolysis of O-Aryl Thionobenzoates: Amine Basicity Combines with Modulation of the Nature of Substituents in the Leaving Group and Thionobenzoate Moiety to Control the Reaction Mechanism-Reference-Cited by-同舟云学术

Aminolysis of O-Aryl Thionobenzoates: Amine Basicity Combines with Modulation of the Nature of Substituents in the Leaving Group and Thionobenzoate Moiety to Control the Reaction Mechanism

Published:2008-09-04 Issue:19 Volume:73 Page:7671-7677
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Um Ik-Hwan¹,Hwang So-Jeong¹,Yoon Sora¹,Jeon Sang-Eun¹,Bae Sun-Kun¹

Affiliation:

1. Department of Chemistry and Nano Science, Ewha Womans University, Seoul 120-750, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801539w

Reference66 articles.

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2. Ingold Lecture. How does a reaction choose its mechanism?

3. Nonlinear structure-reactivity correlations. The reactivity of nucleophilic reagents toward esters

4. The aminolysis of N-aroyl β-lactams occurs by a concerted mechanism

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