Intramolecular kinetic isotope effect in hydride transfer from dihydroacridine to a quinolinium ion. Rejection of a proposed two-step mechanism with a kinetically significant intermediate-Reference-Cited by-同舟云学术

Intramolecular kinetic isotope effect in hydride transfer from dihydroacridine to a quinolinium ion. Rejection of a proposed two-step mechanism with a kinetically significant intermediate

Published:2008 Issue:18 Volume:6 Page:3349
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Perrin Charles L.,Zhao Chen

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2008/OB/B806869K

Reference31 articles.

1. Is the single transition-state model appropriate for the fundamental reactions of organic chemistry?

2. Non-steady-state kinetic study of the SN2 reaction between p-nitrophenoxide ion and methyl iodide in aprotic solvents containing water. Evidence for a 2-step mechanism

3. Resolution of the non-steady-state kinetics of the elimination of HBr from 2-(p-nitrophenyl)ethyl bromide in alcohol/alkoxide media

4. Resolution of the Non-Steady-State Kinetics of the Two-Step Mechanism for the Diels−Alder Reaction between Anthracene and Tetracyanoethylene in Acetonitrile

5. Application of Non-Steady-State Kinetics to Resolve the Kinetics of Proton-Transfer Reactions between Methylarene Radical Cations and Pyridine Bases

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