Metalation vs Nucleophilic Addition in the Reactions of N-Phenethylimides with Organolithium Reagents. Ready Access to Isoquinoline Derivatives via N-Acyliminium Ions and Parham-Type Cyclizations-Reference-Cited by-同舟云学术

Metalation vs Nucleophilic Addition in the Reactions of N-Phenethylimides with Organolithium Reagents. Ready Access to Isoquinoline Derivatives via N-Acyliminium Ions and Parham-Type Cyclizations

Published:1997-04-01 Issue:7 Volume:62 Page:2080-2092
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Collado M. Isabel¹,Manteca Izaskun¹,Sotomayor Nuria¹,Villa María-Jesús¹,Lete Esther¹

Affiliation:

1. Departamento de Química Orgánica, Facultad de Ciencias, Universidad del País Vasco, Apdo. 644, 48080 Bilbao, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo962155o

Reference24 articles.

1. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

2. Combined directed ortho metalation-cross coupling strategies. Design for natural product synthesis

3. Aromatic organolithium reagents bearing electrophilic groups. Preparation by halogen-lithium exchange

4. Aromatic heteroannulation via ortho lithiation-cyclization of N-acyl-2-bromobenzamides

5. A novel and versatile synthesis of 1-aryl-benzocyclobutenols and 1-aryl-benzocyclobutenes

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