DEHYDROHALOGENATION OF SIMPLE ALKYL HALIDES BY STRONG BASE; EVIDENCE OF CARBENE INTERMEDIATES, EXTENT OF α-ELIMINATION1-Reference-Cited by-同舟云学术

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DEHYDROHALOGENATION OF SIMPLE ALKYL HALIDES BY STRONG BASE; EVIDENCE OF CARBENE INTERMEDIATES, EXTENT OF α-ELIMINATION1

Published:1961-01 Issue:2 Volume:83 Page:492-493
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Friedman L.,Berger Joel G.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja01463a061

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1. Sodium Diisopropylamide-Mediated Dehydrohalogenations: Influence of Primary- and Secondary-Shell Solvation;The Journal of Organic Chemistry;2019-08-22

2. Structures of Carbenes and the Stereochemistry of Carbene Additions to Olefins;Topics in Stereochemistry;2007-02-26

3. Rearrangement Pathways of 2-Hydroxy-2-methylpropylidene: An Experimental and Computational Study;The Journal of Organic Chemistry;2002-04-19

4. Role of Spin−Orbit Coupling and Symmetry in Triplet Carbenic Addition Chemistry;The Journal of Physical Chemistry;1996-01-01

5. Competing Radical, Carbanion, and Carbene Intermediates in the Reaction of a Primary Alkyl Halide with Lithium Diisopropylamide.;Acta Chemica Scandinavica;1990

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