Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Pivaloyloximes. Transition-State Differences for the Syn and Anti Eliminations Forming Nitriles-Reference-Cited by-同舟云学术

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Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Pivaloyloximes. Transition-State Differences for the Syn and Anti Eliminations Forming Nitriles

Published:1997-04-01 Issue:7 Volume:62 Page:2230-2233
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cho Bong Rae¹,Cho Nam Soon¹,Lee Sang Kook¹

Affiliation:

1. Department of Chemistry, Korea University, Seoul 136-701, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9618637

Reference20 articles.

1. Saunders, W. H., Jr.; Cockerill, A. F.Mechanism of EliminationReactions; Wiley: New York, 1973; (a) Chapter 1−4, (b) pp 498−531.

2. Stereochemical and base species dichotomies in olefin-forming E2 eliminations

3. Lowry, T. H.; Richardson, K. S.Mechanism and Theory in OrganicChemistry; Harper and Row: New York, 1987; pp 591−616.

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3. Copper immobilized on aminated ferrite nanoparticles by 2-aminoethyl dihydrogen phosphate (Fe3O4@AEPH2-CuII) catalyses the conversion of aldoximes to nitriles;Applied Organometallic Chemistry;2015-08-07

4. Elimination of nitrile from (E)-2,4,6-trinitrobenzaldehyde O-pivaloyloxime promoted by R2NH in MeCN. Effect of β-aryl group on the nitrile-forming transition-state;Kinetics and Catalysis;2011-05

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