A One-Pot Synthesis of 2-Substituted 2,4,5,6-Tetrahydrocyclopentapyrazoles

DOI: 10.1055/s-1988-27695

Source and publish data:

Synthesis p. 742 - 743 (1988)

Update date:2022-08-05

Topics:

Authors:

Aubert, Thierry

Tabyaoui, Badia

Farnier, Michel

Guilard, Roger

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1988-27695

The 2-substituted 2,4,5,6-tetrahydrocyclopentapyrazoles 3 were selectively synthesized by condensation of various in situ generated iminophosphoranes with the 2-azido-1-cyclopentene-1-carboxaldehyde (2).

Full text of DOI:10.1055/s-1988-27695

Products guided by the article

Product name:2,4,5,6-Tetrahydro-2-phenylmethylcyclopentapyrazole

Cas No:84597-88-6

R&D Labs maybe for 84597-88-6

Kraeber & Co GmbH

Contact:+49-4101-3053-0

Address:Waldhofstrasse 14 ,25474 Ellerbek Germany
Taizhou Elitechemie MediPharma Technology Co.,Ltd.

Contact:+86-523-86810021

Address:Building G14,NO.1 Avenue,China Medical City, Taizhou, Jiangsu,China
Hunan Shineway Enterprise Co., Ltd.

Contact:+86-731-86303875

Address:118, Huanghua International Airport Road, Huanghua Town, Changsha, Hunan 410137, China
Shanghai Demand Chemical Co., ltd，China

Contact:86-021-55237578/55239122

Address:Room 3H, No.578, Yingkou Road, Yangpu District, Shanghai, China
SOGA ENTERPRISES ASIA GROUP

Contact:+86-633-8332928

Address:No.1,Huanghai Yilu.Rizhao,Shandong

Relevant to this article

Total Synthesis of the Hypochloesterolemic Agent (+)-Compactin

Doi:10.1021/ja00343a072
(1983)
Highly stable pyrimidine-motif triplex formation at physiological pH values by a bridged nucleic acid analogue

Doi:10.1002/anie.200604857
(2007)
Preparation of advanced intermediates for the synthesis of both methyllycaconitine and racemulsonine via a common intermediate

Doi:10.1016/j.tetlet.2004.12.092
(2005)
Inhibition of prostaglandin synthetase by di- and triphenylethylene derivatives: A structure-activity study

Doi:10.1021/jm00359a014
(1983)
Oligosaccharides as inhibitors of mycobacterial arabinosyltransferases. Di- and trisaccharides containing C-3 modified arabinofuranosyl residues

Doi:10.1016/j.bmc.2004.11.003
(2005)
Generation of Highly Selective, Potent, and Covalent G Protein-Coupled Receptor Kinase 5 Inhibitors

Doi:10.1021/acs.jmedchem.0c01522
(2021)

Article Doi