Synthesis of arylurethans of 1,2-dimethy-3-hydroxymethylhdexahydropyridazine as anticonvulsant agents

DOI: 10.1016/0223-5234(89)90091-3

Source and publish data:

European Journal of Medicinal Chemistry p. 453 - 454 (1989)

Update date:2022-09-26

Topics:

Authors:

Kornet Kornet

Filo Filo

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

Article abstract of DOI:10.1016/0223-5234(89)90091-3

Full text of DOI:10.1016/0223-5234(89)90091-3

Products guided by the article

Product name:3-Pyridazinemethanol,hexahydro-1,2-dimethyl-(9CI)

Cas No:126936-88-7

R&D Labs maybe for 126936-88-7

MENGNA

Contact:18698110882

Address:1303 No2 building,LuoMa Garden,YongAn Road,Hexi District,Tianjin city
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China
Exploiter Molybdenum Co.,Ltd

Contact:86-379-63338609

Address:Jiudian Village,Deting Town,Song County,Luoyang
Hunan Shineway Enterprise Co., Ltd.

Contact:+86-731-86303875

Address:118, Huanghua International Airport Road, Huanghua Town, Changsha, Hunan 410137, China

Relevant to this article

THE VINYLOGOUS CONIA REARRANGEMENT : A MASKED ENE REACTION

Doi:10.1016/S0040-4039(00)99352-3
(1989)
1,10-Phenanthroline Derivatives: A New Ligand Class in the Heck Reaction. Mechanistic Aspects

Doi:10.1021/jo00078a021
(1993)
Large-scale synthesis of all stereoisomers of a 2,3-unsaturated c-glycoside scaffold

Doi:10.1021/jo1022926
(2011)
Synthesis of 1,8-di(1-adamantyl)naphthalenes as single enantiomers stable at ambient temperatures

Doi:10.1039/c0cc03025b
(2011)
Chiral calcium VAPOL phosphate mediated asymmetric chlorination and Michael reactions of 3-substituted oxindoles

Doi:10.1021/ja109824x
(2011)
Autonomously pairing cysteinyl-linked nucleotide analogues with a unique architecture

Doi:10.1021/ja200829s
(2011)

Article Doi