Syntheses of s triazolo [4,3 α] pyrimidine derivatives

DOI: 10.1271/bbb1961.37.441

Source and publish data:

Agricultural and Biological Chemistry p. 441 - 443 (1973)

Update date:2022-08-05

Topics:

Authors:

Okabe Okabe

Taniguchi

Maekawa Maekawa

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

Article abstract of DOI:10.1271/bbb1961.37.441

Full text of DOI:10.1271/bbb1961.37.441

Products guided by the article

Product name:3-benzylsulfanyl-7-methyl-8H-[1,2,4]triazolo[4,3-a]pyrimidin-5-one

Cas No:41266-65-3

R&D Labs maybe for 41266-65-3

Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone
Changzhou Sunlight Pharmaceutical Co., Ltd.

Contact:+86-519-83131668;83139028;83138042;83137041

Address:JiuliStreet, Benniu Town Changzhou City, Jiangsu Province
Sinonine Industry Co.,Ltd

Contact:86+21-56421993

Address:3F,BUILDING 10,NO.2889 JINKE ROAD, SHANGHAI.
Shanghai Goyic Pharmaceutical&Chemical Co,. Ltd

Contact:+86-021-60275964

Address:No. 528 ruiqing road
Nanyang Tianhua pharmaceutical Co.,Ltd.

Contact:+8618639816203

Address:Longsheng Industrial Park

Relevant to this article

Establishment of the chemical equilibria of different types of pyranoanthocyanins in aqueous solutions: Evidence for the formation of aggregation in pyranomalvidin-3- O -coumaroylglucoside-(+)-catechin

Doi:10.1021/jp1045673
(2010)
Biosynthesis of Indole Diterpene Lolitrems: Radical-Induced Cyclization of an Epoxyalcohol Affording a Characteristic Lolitremane Skeleton

Doi:10.1002/anie.202007280
(2020)
Succinamide derivatives ameliorate neuroinflammation and oxidative stress in scopolamine-induced neurodegeneration

Doi:10.3390/biom10030443
(2020)
Doi:10.1021/ja00790a087
(1973)
Doi:10.1021/ja00786a034
(1973)
Fast and efficient reductive amination of aldehydes by NaBH ₄/B(OH)₃ and NaBH₄/Al(OH)₃

Doi:10.1002/jccs.201300138
(2013)

Article Doi