On the origin of the enhanced reactivity of α-halocarbonyl compounds in SN2 processes-Reference-Cited by-同舟云学术

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On the origin of the enhanced reactivity of α-halocarbonyl compounds in SN2 processes

Published:2003-11 Issue:1-3 Volume:663 Page:47-58
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Gineityte V.

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference24 articles.

1. Structure and Mechanism in Organic Chemistry;Ingold,1953

2. Advanced Organic Chemistry, Reactions, Mechanisms and Structure;March,1985

3. Einfürung in die Elektronentheorie Organisch Chemischen Reaktionen;Becker,1974

4. Organic Reaction Mechanisms. A Step by Step Approach;Edenborough,1999

5. Perspectives on Structure and Mechanism in Organic Chemistry;Carroll,1998

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1. Redox Signaling by Reactive Electrophiles and Oxidants;Chemical Reviews;2018-08-27

2. A Common Selection Rule for Organic Reactions in Terms of Signs of Direct and Indirect Interorbital Interactions;Zeitschrift für Naturforschung A;2009-02-01

3. Addition of nucleophile to bent bonds of the carbonyl group;Lithuanian Journal of Physics;2009

4. Mechanism of the reaction of neutral and anionic N-nucleophiles with α-halocarbonyl compounds;Russian Chemical Bulletin;2007-06

5. Enantiodiscrimination of racemic electrophiles by diketopiperazine enolates: asymmetric synthesis of methyl 2-amino-3-aryl-butanoates and 3-methyl-aspartates;Tetrahedron;2006-08

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