Studies on 2,5-diaryl-2,4-dihydro-3H-pyrazol-3-ones. II. Synthesis of 4-cycloalkyl-2,5-diaryl-2,4-dihydro-3H-pyrazol-3-ones using the tautomeric properties of 2,5-diaryl-2,4-dihydro-3H-pyrazol-3-ones

DOI: 10.1248/cpb.33.3623

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 3623 - 3634 (1985)

Update date:2022-08-05

Topics:

Authors:

Matsugo Matsugo

Saito Saito

Takamizawa

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

Article abstract of DOI:10.1248/cpb.33.3623

Full text of DOI:10.1248/cpb.33.3623

NII-Electronic Library Service

Products guided by the article

Product name:2-(4'-chloro-phenyl)-4-cycloheptyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one

Cas No:103897-02-5

R&D Labs maybe for 103897-02-5

FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com
Advanced Biotech

Contact:+1-973-357-0577

Address:10 Taft Rd.
HuiFeiChem PharmaTech Co.Ltd

Contact:0510-85393305

Address:1619 Huishan Avenue, Huishan District, Wuxi,
Beijing eternalchem Co,. Ltd

Contact:+86-10-59484199

Address:No.58-A1026 Liangguan Street
Wuxi Innopal International Trade CO.,LTD

Contact:+86-510-80711901-8003

Address:Room 402,Building 5,Longze Garden,No.17,South huanjiu Road,Yixing City, Jiangsu,China

Relevant to this article

A simple method for the synthesis of 5-substituted 2-cyanofurans

Doi:10.1023/A:1019544726068
(2002)
Doi:10.1016/S0022-328X(00)85507-2
(1976)
Facile and selective synthesis of propargylic amines and 1,6-diynes: One-pot three-component coupling reactions of alkynylsilanes, aldehydes and amines by a cooperative catalytic system comprised of CuCl and Cu(OTF) ₂

Doi:10.1055/S-2008-1077790
(2008)
Stereospecific synthesis of the enantiomers of verapamil and gallopamil

Doi:10.1021/jo00383a026
(1987)
Bradykinin B₁ receptor antagonists: An α-hydroxy amide with an improved metabolism profile

Doi:10.1016/j.bmcl.2008.07.126
(2008)
Synthesis of new sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors

Doi:10.1016/j.bmc.2008.07.073
(2008)

Article Doi