Heteroaromatic Annulation of 2-Methyl/2-Cyanomethylbenzimidazole Dianions with α-Oxoketene Dithioacetals: A Highly Regioselective Synthetic Protocol for 1,2- and 2,3-Substituted/Annulated Pyrido[1,2-a]benzimidazoles-Reference-Cited by-同舟云学术

Heteroaromatic Annulation of 2-Methyl/2-Cyanomethylbenzimidazole Dianions with α-Oxoketene Dithioacetals: A Highly Regioselective Synthetic Protocol for 1,2- and 2,3-Substituted/Annulated Pyrido[1,2-a]benzimidazoles

Published:2003-03-27 Issue:9 Volume:68 Page:3498-3506
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Panda Kausik¹,Suresh J. R.¹,Ila H.¹,Junjappa H.¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo026786w

Reference62 articles.

1. Heterocyclization of Functionalized Vinylic Derivatives of Imidazo[1,2-a]pyridines

2. A Facile Access to 2-Methylthio/Alkoxy/Amino-3-acylimidazo[1,2-a]pyridines Based on Cupric Chloride Promoted Oxidative Ring Closure of α-Oxoketene N,S-, N,O-, and N,N-Acetals

3. Derivatives of Imidazole. I. Synthesis and Reactions of Imidazo[1,2-α]pyridines with Analgesic, Antiinflammatory, Antipyretic, and Anticonvulsant Activity

4. Isolation and structure determination of mutagenic substances in L-glutamic acid pyrolysate.

5. Cardiotonic agents. 1. Novel 8-aryl substituted imidazo[1,2-a]- and -[1,5-a]pyridines and imidazo[1,5-a]pyridinones as potential positive inotropic agents

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