An Expeditious and Efficient Synthesis of Highly Functionalized [1,6]-Naphthyridines under Catalyst-Free Conditions in Aqueous Medium-Reference-Cited by-同舟云学术

An Expeditious and Efficient Synthesis of Highly Functionalized [1,6]-Naphthyridines under Catalyst-Free Conditions in Aqueous Medium

Published:2011-08-01 Issue:17 Volume:13 Page:4664-4667
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mukhopadhyay Chhanda¹,Das Paramita¹,Butcher Ray J.¹

Affiliation:

1. Department of Chemistry, University of Calcutta, 92 APC Road, Kolkata-700009, India, and Department of Chemistry, Howard University, Washington, D.C. 20059, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol201877v

Reference32 articles.

1. Pyridoacridine Alkaloids Inducing Neuronal Differentiation in a Neuroblastoma Cell Line, from Marine Sponge Biemna fortis

2. A formal total synthesis of the marine alkaloid aaptamine

3. Antiproliferative activity of novel benzo[b][1,6]naphthyridines in human solid tumor cell lines

4. The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore

5. Allosteric inhibitors of Akt1 and Akt2: Discovery of [1,2,4]triazolo[3,4-f][1,6]naphthyridines with potent and balanced activity

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