1,2,4-Oxadiazoles. IV. Synthesis and pharmacological properties of a series of substituted aminoalkyl-1,2,4-oxadiazoles.

DOI: 10.1021/jm50018a009

Source and publish data:

Journal of medicinal and pharmaceutical chemistry p. 351 - 367 (1961)

Update date:2022-09-26

Topics:

Authors:

PALAZZO PALAZZO

TAVELLA TAVELLA

STRANI STRANI

SILVESTRINI

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

Article abstract of DOI:10.1021/jm50018a009

Full text of DOI:10.1021/jm50018a009

Products guided by the article

Product name:ethyl-(3-phenyl-[1,2,4]oxadiazol-5-ylmethyl)-amine

Cas No:91331-82-7

R&D Labs maybe for 91331-82-7

WD Silicone Co., Ltd

Contact:+86-27-87204219, +86-27-87215023

Address:2402, HuiGu Space-time Building, 8 Forest Road, East Lake Hi-Tech Development Zone
Weifang Jahwa Chemical Co.,Ltd

Contact:0086-536-8897731,8897730

Address:No.5166 East Dongfeng Street,Weifang,Shandong,China
A.M FOOD CHEMICAL CO., LIMITED

Contact:86-531-87100375

Address:20Floor，Bblock，1Building，pharma-valley，Jinan，China
MiHecb Bio-Tech Co., Ltd.

Contact:+86-0592 5353131

Address:No.56 Guani Road Software Park 2,Siming District
HENAN NEW BLUE CHEMICAL CO.,LTD

website:http://www.newbluechem.com

Contact:86-371-55170693/55170694

Address:Zhengzhou International Trade New Territory,Jinshui District,Zhengzhou ,China

Relevant to this article

Catalytic Action of Metal Salts in the Amination of 5,8-Quinolinediones

Doi:10.1246/cl.1986.1059
(1986)
Palladium-catalyzed controlled carbopalladation of benzyne

Doi:10.1021/ja001205a
(2000)
Novel fluorinated chromones

Doi:10.1016/S0022-1139(00)80470-4
(1993)
An Efficient and Stereoselective Synthesis of 2,3-Dihydroindoles via 1,5-Electrocyclization

Doi:10.1021/ja00405a088
(1981)
Stereospecific diphosphination of activated acetylenes: A general route to backbone-functionalized, chelating 1,2-diphosphinoethenes

Doi:10.1021/om060716o
(2006)
One-pot carbonyl reduction and carbonate formation using sodium borohydride in dialkyl carbonate solvents

Doi:10.1016/j.tetlet.2019.151203
(2019)

Article Doi