Efficient, “Tin-Free” Radical Cyclization to Aromatic Systems. Synthesis of 5,6,8,9,10,11- Hexahydroindolo[2,1-a]isoquinolines-Reference-Cited by-同舟云学术

Efficient, “Tin-Free” Radical Cyclization to Aromatic Systems. Synthesis of 5,6,8,9,10,11- Hexahydroindolo[2,1-a]isoquinolines

Published:2004-05-01 Issue:11 Volume:69 Page:4001-4004
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Menes-Arzate Martha¹,Martínez Roberto¹,Cruz-Almanza Raymundo¹,Muchowski Joseph M.¹,Osornio Yazmin M.¹,Miranda Luis D.¹

Affiliation:

1. Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán, México D. F. 04510, Mexico, and Chemistry, Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, California 94304-1320 lmiranda@servidor.unam.mx

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0497048

Reference39 articles.

1. The Mechanism of Bu3SnH-Mediated Homolytic Aromatic Substitution

2. Intramolecular free-radical substitution of pyridinium rings

3. Synthesis of imidazo[4,5-c]quinolin-4(5H)-oneviaradical cyclization

4. Oxidative radical cyclization to pyrroles under reducing conditions. Reductive desulfonylation of α-sulfonylpyrroles with tri-n-butyltin hydride

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