Quantum Yields of the Initiation Step and Chain Propagation Turnovers in SRN1 Reactions: Photostimulated Reaction of 1-Iodo-2-methyl-2-phenyl Propane with Carbanions in DMSO-Reference-Cited by-同舟云学术

Quantum Yields of the Initiation Step and Chain Propagation Turnovers in SRN1 Reactions: Photostimulated Reaction of 1-Iodo-2-methyl-2-phenyl Propane with Carbanions in DMSO

Published:2000-10-01 Issue:21 Volume:65 Page:7175-7182
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Argüello Juan E.¹,Peñéñory Alicia B.¹,Rossi Roberto A.¹

Affiliation:

1. INFIQC, Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000 Córdoba, Argentina

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001141m

Reference49 articles.

1. Mechanisms and reactivity in electron transfer induced aromatic nucleophilic substitution. Recent advances.

2. “Thermal” SRN1 Reactions: How Do They Work? Novel Evidence that the Driving Force Controls the Transition between Stepwise and Concerted Mechanisms in Dissociative Electron Transfers

3. Dark reactions of halobenzenes with pinacolone enolate ion. Evidence for a thermally induced aromatic SRN1 reaction

4. SRN1 mechanism in heteroaromatic nucleophilic substitution. Reactions involving halogenated pyrimidines, pyridazines, and pyrazines

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