Specific enzyme inhibitors in vitamin biosynthesis. I. The synthesis of 8-substituted pyrido(2,3-d)pyrimidines.

DOI: 10.1039/P19720001041

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 1041 - 1050 (1972)

Update date:2022-08-03

Topics:

Authors:

Paterson

Wood Wood

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

Article abstract of DOI:10.1039/P19720001041

Full text of DOI:10.1039/P19720001041

View Online / Journal Homepage / Table of Contents for this issue

View Online

Products guided by the article

Product name:8-(2-hydroxy-ethyl)-5-(4-nitro-styryl)-8H-pyrido[2,3-d]pyrimidine-2,4-dione

Cas No:36075-37-3

R&D Labs maybe for 36075-37-3

Beijing eternalchem Co,. Ltd

Contact:+86-10-59484199

Address:No.58-A1026 Liangguan Street
Xinyanhe Pharmatech Co.,Ltd

Contact:+86-519-8525-2752

Address:Changzhou
SHANXI JINJIN CHEMICAL INDUSTRIAL CO.,LTD

website:http://www.jinjingroup.com

Contact:86-574-13989382828

Address:Economic And Technological Development Zone,Hejin?City,Shanxi Province?,China
Richest Group Ltd.

Contact:+86 21 5017 5386

Address:No 999,Jiangyue Rd, Minhang Dist ,201114,Shanghai ,China
Jintan Jinnuo Chemical Co., Ltd.

Contact:+86-519-80199901

Address:Room 1804, Building 1, Huacheng Business Plaza, Jintan, Jiangsu, China

Relevant to this article

Development of the β-lactam type molecular scaffold for selective estrogen receptor α modulator action: synthesis and cytotoxic effects in MCF-7 breast cancer cells

Doi:10.1080/14756366.2016.1210136
(2016)
(+)-(R)- and (?)-(S)-Perhexiline maleate: Enantioselective synthesis and functional studies on Schistosoma mansoni larval and adult stages

Doi:10.1016/j.bioorg.2020.104067
(2020)
Doi:10.1007/BF00472361
()
Doi:10.1039/c29690000816
(1969)
Doi:10.1016/0040-4020(72)88063-3
(1972)
Effect of o-difluoro and p-methyl substituents on the structure, optical properties and anti-inflammatory activity of phenoxy thiazole acetamide derivatives: Theoretical and experimental studies

Doi:10.1016/j.molstruc.2019.127024
(2020)

Article Doi