Mode of formation of quinoxaline versus 2[1H]-quinoxalin-one rings from dehydro-D-erythorbic acid

DOI: 10.1016/0008-6215(92)80039-4

Source and publish data:

Carbohydrate Research p. 59 - 66 (1992)

Update date:2022-09-26

Topics:

Authors:

Mousaad Mousaad

Rashed Rashed

Hamid Hamid

El Kilany

Sayed Sayed

El Ashry

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

Article abstract of DOI:10.1016/0008-6215(92)80039-4

The mode of formation of the quinoxaline versus 2[1H]-quinoxalinone rings by the reaction of o-diamines with dehydro-D-erythorbic acid has been investigated. The study was carried out by using one and two molar equivalents of 1,2-diamino-4,5-dimethylbenze

Full text of DOI:10.1016/0008-6215(92)80039-4

Products guided by the article

Product name:2-(2-amino-4,5-dimethylphenylcarbamoyl)-3-(D-erythro-glycerol-1-yl)-6,7-dimethylquinoxaline

Cas No:140840-31-9

R&D Labs maybe for 140840-31-9

shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD

Contact:29-63685658 63685359

Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China
Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
X.T.Y Environ-Tech Co.,Ltd

Contact:+86-310-7092106

Address:Quzhou Modern & New Industrial Park, Handan, Hebei 057250, China
Hangzhou Showland Technology Co., Ltd.

Contact:86-571-88920516

Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA

Relevant to this article

Identification of a chemical probe for bromo and extra C-terminal bromodomain inhibition through optimization of a fragment-derived hit

Doi:10.1021/jm3010515
(2012)
Microwave-assisted synthesis and in vitro antibacterial activity of novel steroidal thiosemicarbazone derivatives

Doi:10.1016/j.bmcl.2012.09.083
(2012)
A novel and convenient method for the synthesis of new derivatives of pyrido[3,2-e]pyrrolo[1,2-a][1,4]diazepine-6,11-dione

Doi:10.1016/j.tet.2012.09.079
(2012)
Efficient asymmetric synthesis of trifluoromethylated β- aminophosphonates and their incorporation into dipeptides

Doi:10.1039/c2cc36702e
(2012)
Full stereochemical determination of ajudazols a and b by bioinformatics gene cluster analysis and total synthesis of ajudazol B by an asymmetric ortholithiation strategy

Doi:10.1021/ja309685n
(2012)
Synthesis of (+/-)-Isopiperitenol by Fluoride Ion Mediated Cyclization of Allylsilane Moiety Incorporated in Terpene Aldehydes

Doi:10.1246/bcsj.65.929
(1992)

Article Doi