Solid phase synthesis of 1,5-disubstituted pyrazole-4-hydroxamic acids and pyrazole-4-carboxamides via direct amidation of β-ketoesters-Reference-Cited by-同舟云学术

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Solid phase synthesis of 1,5-disubstituted pyrazole-4-hydroxamic acids and pyrazole-4-carboxamides via direct amidation of β-ketoesters

Published:2012-01 Issue:3 Volume:53 Page:267-270
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zhai Weixu,Gerritz Samuel W.,Sofia Michael J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)

2. Estrogen pyrazoles: defining the pyrazole core structure and the orientation of substituents in the ligand binding pocket of the estrogen receptor

3. Chapter 24. Inhibition of Matrix Metalloproteinases.

4. Pendri, A.; Gerritz, S.W; Dodd, D.; Sun, C.; U.S Pat. Appl. Publ. 2005, CODEN: USXXCO US 2005080087 A1 20050414.

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