Kinetic arguments for the existence of hydrogen bonded carbanion intermediates during dehydrohalogenation reactions of C6H5CHClCF2Y-Reference-Cited by-同舟云学术

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Kinetic arguments for the existence of hydrogen bonded carbanion intermediates during dehydrohalogenation reactions of C6H5CHClCF2Y

Published:1973-03 Issue:6 Volume:95 Page:2029-2030
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Koch H. F.,Dahlberg D. B.,Toczko A. G.,Solsky R. L.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00787a061

Cited by 24 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. A highly efficient room temperature non-organometallic route for the synthesis of α,β,β-trifluorostyrenes by dehydrohalogenation;Tetrahedron Letters;2003-08

2. Use of Kinetic Isotope Effects in Mechanism Studies. 5.1 Isotope Effects and Element Effects Associated with Hydron-Transfer Steps during Alkoxide-Promoted Dehydrohalogenations;Journal of the American Chemical Society;1997-10-01

3. Carbon−Oxygen Hydrogen Bonding in Dehydrohalogenation Reactions: PM3 Calculations on Polyhalogenated Phenylethane Derivatives;The Journal of Organic Chemistry;1997-10-01

4. Hydrogen fluoride abstraction from vicinal difluoroalkanes : Reaction conditions andsyn/anti-stereoselectivity;Tetrahedron;1988-01

5. Mechanism of base-promoted eliminative fragmentations of 2-alkyl-3-phenyloxaziridines;The Journal of Organic Chemistry;1986-10

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