3-substituted-2-benzoxazolinones.

DOI: 10.1002/jps.2600571029

Source and publish data:

Journal of Pharmaceutical Sciences p. 1763 - 1768 (1968)

Update date:2022-09-26

Topics:

Authors:

Sam Sam

Valentine

Richmond

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

Article abstract of DOI:10.1002/jps.2600571029

Full text of DOI:10.1002/jps.2600571029

Products guided by the article

Product name:5-trifluoromethyl-benzooxazol-2-ylamine

Cas No:20844-69-3

R&D Labs maybe for 20844-69-3

Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Jinan Yijialian Economic and Trade Development Co., Ltd.

Contact:+86 0531-66729596

Address:jinan
jiangsu senxuan pharmaceutical and chemical co.,ltd

Contact:86-523-87982810

Address:hongqiao industrial zone,taixing,jiangsu china
Yingkou Sanzheng Organic Chemical Co. Ltd.

Contact:+86-417-3638818

Address:25 Gengxinli Village, Daqing Road, Yingkou, Liaoning, China
Chemtrade International ( China )

Contact:+86-532-86893005

Address:Rm 2-501, Huaxia Zonghe Building, No. 410 JInggangshan Road, Huangdao

Relevant to this article

A SYNTHESIS OF TETRAHYDROOXOCRININE METHINE.

Doi:10.1248/cpb.13.427
(1965)
Organocatalysis in conjugate amine additions. Synthesis of β-amino acid derivatives

Doi:10.1021/ja071739c
(2007)
Synthesis of the antibiotically active part of agrocin 84

Doi:10.1016/S0040-4039(98)00888-0
(1998)
A new method for the synthesis of dithiocarbamates by CuI-catalyzed coupling reaction

Doi:10.1016/j.tetlet.2007.03.168
(2007)
Doi:10.1016/S0040-4039(00)75558-4
(1968)
Antitumor activity of ribonuclease multimers created by site-specific covalent tethering

Doi:10.1021/bc100292x
(2010)

Article Doi