Kinetic Studies on Nucleophilic Substitution Reactions of O-Aryl Thionobenzoates with Azide, Cyanide, and Hydroxide: Contrasting Reactivity and Mechanism-Reference-Cited by-同舟云学术

Kinetic Studies on Nucleophilic Substitution Reactions of O-Aryl Thionobenzoates with Azide, Cyanide, and Hydroxide: Contrasting Reactivity and Mechanism

Published:2009-01-02 Issue:3 Volume:74 Page:1212-1217
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Um Ik-Hwan¹,Kim Eun-Hee¹,Lee Ji-Youn¹

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/jo802446y

Reference68 articles.

1. aMarch, J.Advanced Organic Chemistry,4th ed.;Wiley:New York,1992; pp330−335

2. bLowry, T. H.; Richardson, K. S.Mechanism and Theory in Organic Chemistry, 3rd ed.Harper and Row:New York,1987; pp710−723

3. SN2 Mechanism for Alcoholysis, Aminolysis, and Hydrolysis of Acetyl Chloride

4. Solvolyses of para-substituted benzoyl chlorides in trifluoroethanol and in highly aqueous media

5. Nucleophilic substitution at trigonal carbon. Part 4. Substituent effects in the reactions of aliphatic acyl chlorides with methanol and phenol in acetonitrile

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