Tandem Pseudopericyclic Reactions: [1,5]-X Sigmatropic Shift/6π-Electrocyclic Ring Closure Converting N-(2-X-Carbonyl)phenyl Ketenimines into 2-X-Quinolin-4(3H)-ones-Reference-Cited by-同舟云学术

Tandem Pseudopericyclic Reactions: [1,5]-X Sigmatropic Shift/6π-Electrocyclic Ring Closure Converting N-(2-X-Carbonyl)phenyl Ketenimines into 2-X-Quinolin-4(3H)-ones

Published:2006-09-19 Issue:21 Volume:71 Page:8126-8139
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alajarín Mateo¹,Ortín María-Mar¹,Sánchez-Andrada Pilar¹,Vidal Ángel¹

Affiliation:

1. Departamento de Química Orgánica, Facultad de Química, Campus de Espinardo, Universidad de Murcia, 30100 Murcia, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061286e

Reference101 articles.

1. First radical addition onto ketenimines: a novel synthesis of indoles

2. Intramolecular addition of benzylic radicals onto ketenimines. Synthesis of 2-alkylindoles

3. Persistent radical effect in the intramolecular addition of benzylic radicals onto ketenimines: selective cross-coupling of α-(indol-2-yl)benzyl radicals with the 1-cyano-1-methylethyl radical

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