
Monatshefte fur Chemie p. 1027 - 1030 (1988)
Update date:2022-08-03
Topics: Melting point Yield Catalyst Synthetic route Intramolecular cyclization Carbonyl group Chromatography Recrystallization Nucleophilic substitution Cyclization Aryl group Oxadiazole Reaction Mechanism Spectroscopic Analysis Heterocyclic compound
Davidson, John S.
Some 1-aroyl-4,4-dialkylsemicarbazides have been prepared by reacting aroyl-hydrazides with dimethyl- or diethyl-carbamoyl chloride.In boiling DMF they lose dimethylamine or diethylamine to give 5-aryl-1,3,4-oxadiazol-2(3H)-ones. - Keywords: 1-Aroyl-4,4-d
View MoreHangzhou Pharma & Chem Co.,Ltd.
Contact:+86-571-87040515
Address:No,139Qingchun Rd
Jinan Hongfangde Pharmatech Co.LTD
Contact:0531-88870908
Address:F Bldg,750#,Shunhua Rd,New&High-tech Zone,Jinan,Shandong,China 250101
Ceresking Ecology & Technology co.,ltd
Contact:86 22 66218397
Address:Room 1613, Zheshang Mansion, No. 1988, Yingbin Avenue, Binhai New District, Tianjin,China.
Liaoyang hengye Chemical Co., Ltd.
Contact:86-419-5850866
Address:North Old Xiaoxiao Road,Yantai District, Dengta, Liaoyang, Liaoning, China
Zhejiang Chemline International Co., Ltd.
Contact:+86-571-88062298
Address:Hengdian Industry Area, Dongyang, Zhejiang, China
Doi:10.1021/ic4021417
(2013)Doi:10.1021/ja00191a027
(1989)Doi:10.1016/S0040-4020(01)81431-9
(1988)Doi:10.1002/ejoc.200900777
(2009)Doi:10.1016/S0040-4020(01)85886-5
(1988)Doi:10.1246/cl.161102
(2017)