Effect of Amine Nature on Reaction Rate and Mechanism in Nucleophilic Substitution Reactions of 2,4-Dinitrophenyl X-Substituted Benzenesulfonates with Alicyclic Secondary Amines-Reference-Cited by-同舟云学术

Effect of Amine Nature on Reaction Rate and Mechanism in Nucleophilic Substitution Reactions of 2,4-Dinitrophenyl X-Substituted Benzenesulfonates with Alicyclic Secondary Amines

Published:2004-04-01 Issue:9 Volume:69 Page:3166-3172
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Um Ik-Hwan¹,Chun Sun-Mee¹,Chae Ok-Mi¹,Fujio Mizue¹,Tsuno Yuho¹

Affiliation:

1. Department of Chemistry, Ewha Womans University, Seoul 120-750, Korea, Department of Chemistry, Kunsan National University, Kunsan 573-701, Korea, and Institute for Materials Chemistry and Engineering, Kyushu University, Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo049812u

Reference87 articles.

1. Identification of the active catalyst in the rhodium porphyrin-mediated cyclopropanation of alkenes

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

Cited by 73 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Theoretical investigation of nucleophilic substitution reaction of phenyl carbonyl isothiocyanates with pyridines in gas and polar aprotic solvent;Physical Chemistry Chemical Physics;2024

2. Crystal structure of 2,4-dinitrophenyl 2,4,6-trimethylbenzenesulfonate;European Journal of Chemistry;2022-06-30

3. Kinetic study on pyridinolysis of aryl benzenesulfonates: factors governing regioselectivity and reaction mechanism;Canadian Journal of Chemistry;2022-05

4. Nucleophilicities of para‐substituted aniline radical cations in acetonitrile: Kinetic investigation and structure–reactivity relationships;International Journal of Chemical Kinetics;2021-08-18

5. Nucleophilic Neutralization of Organophosphates: Lack of Selectivity or Plenty of Versatility?;The Chemical Record;2021-06-11