An efficient, high yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones-Reference-Cited by-同舟云学术

An efficient, high yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones

Published:2006-01 Issue:5 Volume:47 Page:813-816
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bose D. Subhas,Kumar Racherla Kishore

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. Practical Route to a New Class of LTD4 Receptor Antagonists

2. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives

3. 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities

4. Synthesis and pharmacological properties of some quinoline derivatives

5. Quinolines as potent 5-lipoxygenase inhibitors: Synthesis and biological profile of L-746,530

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