Structure and Reactivity of trans-Bis[2-(2-chloroethyl)pyridine]palladium Chloride (1). A Study on the Elimination Reaction of 1 and 2-(2-Chloroethyl)pyridine Induced by Quinuclidine in Acetonitrile-Reference-Cited by-同舟云学术

Structure and Reactivity of trans-Bis[2-(2-chloroethyl)pyridine]palladium Chloride (1). A Study on the Elimination Reaction of 1 and 2-(2-Chloroethyl)pyridine Induced by Quinuclidine in Acetonitrile

Published:2005-11-18 Issue:26 Volume:70 Page:10688-10692
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alunni Sergio¹,Bellachioma Gianfranco¹,Clot Eric¹,Del Giacco Tiziana¹,Ottavi Laura¹,Zuccaccia Daniele¹

Affiliation:

1. Dipartimento di Chimica, Università degli Studi di Perugia, via Elce di Sotto 8, 06123 Perugia, Italy, and LSDSMS (UMR 5636 CNRS), case courrier 14, Institut Gerhardt, Université Montpellier 2, F-34095 Montpellier Cedex 5, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo051324e

Reference27 articles.

1. Mechanism and proton activating factors in base-induced β-elimination reactions of N-[2-(4-pyridyl)ethyl]quinuclidinium and N-[2-(2-pyridyl)ethyl]quinuclidinium salts †

2. Mechanism and proton activating factors in base-induced β-elimination reactions of 2-(2-chloroethyl)pyridine †

3. Catalysis of the β-Elimination of HF from Isomeric 2-Fluoroethylpyridines and 1-Methyl-2-fluoroethylpyridinium Salts. Proton-Activating Factors and Methyl-Activating Factors as a Mechanistic Test To Distinguish between Concerted E2 and E1cb Irreversible Mechanisms

4. Use of solvent isotope effect to identify an intermediate carbanion in the β-elimination reactions from N-[2-(4-pyridyl)ethyl]quinuclidinium and N-[2-(2-pyridyl)ethyl]quinuclidinium induced by acetohydroxamate/acetohydroxamic acid buffers

5. Mechanisms of Acid−Base Catalysis of β-Elimination Reactions in Systems Activated by a Pyridine Ring

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