Synthesis of Functionalized 1,4-Cyclohexadienes through Intramolecular Anionic Dearomatization of N-Alkyl-N-benzyldiphenylphosphinamides. Insight into the Reaction Mechanism-Reference-Cited by-同舟云学术

Synthesis of Functionalized 1,4-Cyclohexadienes through Intramolecular Anionic Dearomatization of N-Alkyl-N-benzyldiphenylphosphinamides. Insight into the Reaction Mechanism

Published:2003-05-01 Issue:11 Volume:68 Page:4472-4485
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fernández Ignacio¹,Forcén-Acebal Angela¹,García-Granda Santiago¹,López-Ortiz Fernando¹

Affiliation:

1. Área de Química Orgánica, Universidad de Almería, Carretera de Sacramento, 04120, Almería, Spain, and Departamento de Química Física y Analítica, Universidad de Oviedo, Avenida Julián Clavería 8, 33071 Oviedo, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0342370

Reference109 articles.

1. Organic Polyvalent Iodine Compounds

2. Dearomatisation of 2-naphthol by oxidative nucleophilic substitution and oxidative electrophilic substitution

3. Intramolecular anodic carbon-carbon bond-forming reactions of oxidized phenol intermediates leading to spirodienones. Structural effects on reactivity and evidence for a phenoxonium ion intermediate

4. Oxidized Arenol Intermediates in Intermolecular Carbon−Carbon Bond Formation. Naphthoid Cyclohexa-2,4-dienones via Oxidative Nucleophilic Substitution

5. Novel tert-Butyl Migration in Copper-Mediated Phenol Ortho-Oxygenation Implicates a Mechanism Involving Conversion of a 6-Hydroperoxy-2,4-cyclohexadienone Directly to an o-Quinone

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