Selenium-catalyzed carbonylation of nitroarenes to symmetrical 1,3-diarylureas under solvent-free conditions

doi:10.1016/j.molcata.2006.03.048

DICP OpenIR

	Selenium-catalyzed carbonylation of nitroarenes to symmetrical 1,3-diarylureas under solvent-free conditions
	Wang, XF; Li, P; Yuan, XH; Lu, SW
Keyword	Selenium Carbonylation Solvent-free Nitroarenes
Source Publication	JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
	2006-07-01
DOI	10.1016/j.molcata.2006.03.048
Volume	253 Issue:1-2 Pages:261-264
Indexed By	SCI
Subtype	Article
WOS Headings	Science & Technology ; Physical Sciences
WOS Subject	Chemistry, Physical
WOS Research Area	Chemistry
WOS Keyword	AROMATIC NITRO-COMPOUNDS ; TEMPERATURE IONIC LIQUIDS ; REDUCTIVE CARBONYLATION ; OXIDATIVE CARBONYLATION ; CARBON-MONOXIDE ; UNSYMMETRIC PHENYLUREAS ; AMINES ; UREAS ; DIOXIDE ; DERIVATIVES
Abstract	An efficient synthetic system without solvent was developed for the selenium-catalyzed carbonylation of nitroarenes with CO to afford symmetrical 1,3-diarylureas in high yields. Additionally, three herbicides were readily obtained from diarylureas and dimethyl-amine. (c) 2006 Elsevier B.V. All rights reserved.
Language	英语
WOS ID	WOS:000238502400038
Citation statistics	Cited Times:23[WOS] [WOS Record] [Related Records in WOS]
Document Type	期刊论文
Identifier	http://cas-ir.dicp.ac.cn/handle/321008/140071
Collection	中国科学院大连化学物理研究所
Affiliation	Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116011, Liaoning, Peoples R China
Recommended Citation GB/T 7714	Wang, XF,Li, P,Yuan, XH,et al. Selenium-catalyzed carbonylation of nitroarenes to symmetrical 1,3-diarylureas under solvent-free conditions[J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL,2006,253(1-2):261-264.
APA	Wang, XF,Li, P,Yuan, XH,&Lu, SW.(2006).Selenium-catalyzed carbonylation of nitroarenes to symmetrical 1,3-diarylureas under solvent-free conditions.JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL,253(1-2),261-264.
MLA	Wang, XF,et al."Selenium-catalyzed carbonylation of nitroarenes to symmetrical 1,3-diarylureas under solvent-free conditions".JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL 253.1-2(2006):261-264.

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