A concise synthetic strategy to functionalized chromenones via [5+1] heteroannulation and facile C–N/C–S/C–O bond formation with various nucleophiles-Reference-Cited by-同舟云学术

A concise synthetic strategy to functionalized chromenones via [5+1] heteroannulation and facile C–N/C–S/C–O bond formation with various nucleophiles

Published:2011-01 Issue:2 Volume:52 Page:254-257
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Savant Mahesh M.,Gowda Neetha S.,Pansuriya Akshay M.,Bhuva Chirag V.,Kapuriya Naval,Anandalwar Sridhar M.,Prasad Shashidhara J.,Shah Anamik,Naliapara Yogesh T.

Funder

FIST-DST

SAP-UGC

DST New Delhi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference44 articles.

1. Structural Studies on Bioactive Compounds. 40. Synthesis and Biological Properties of Fluoro-, Methoxyl-, and Amino-Substituted 3-Phenyl-4H-1-benzopyran-4-ones and a Comparison of Their Antitumor Activities with the Activities of Related 2-Phenylbenzothiazoles

2. Antiallergic activity of 4-hydroxy-3-nitrocoumarins

3. Selective Benzopyranone and Pyrimido[2,1-a]isoquinolin-4-one Inhibitors of DNA-Dependent Protein Kinase: Synthesis, Structure−Activity Studies, and Radiosensitization of a Human Tumor Cell Line in Vitro

4. Synthesis and hybridization properties of the conjugates of oligonucleotides and stabilization agents. Part 3☆

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