Reaction of α-Oxoketene-N,S-arylaminoacetals with Vilsmeier Reagents: An Efficient Route to Highly Functionalized Quinolines and Their Benzo/Hetero-Fused Analogues-Reference-Cited by-同舟云学术

Reaction of α-Oxoketene-N,S-arylaminoacetals with Vilsmeier Reagents: An Efficient Route to Highly Functionalized Quinolines and Their Benzo/Hetero-Fused Analogues

Published:2003-04-09 Issue:10 Volume:68 Page:3966-3975
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mahata P. K.¹,Venkatesh C.¹,Syam Kumar U. K.¹,Ila H.¹,Junjappa H.¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kanpur-208016, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034053l

Reference53 articles.

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3. Structure−Activity Relationships for Acridine-Substituted Analogues of the Mixed Topoisomerase I/II Inhibitor N-[2-(Dimethylamino)ethyl]acridine-4-carboxamide

4. Friedländer Synthesis of Chiral Alkyl-Substituted 1,10-Phenanthrolines

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