Synthesis of diaryl selenides using the in situ reagent SeCl2

Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/11439

Title:	Synthesis of diaryl selenides using the in situ reagent SeCl2
Authors:	ZADE, SS PANDA, S SINGH, HB WOLMERSHAUSER, G
Keywords:	free-radical synthesis x-ray structures organoselenium compounds coordination chemistry peroxidase-activity diselenides ebselen analogs antioxidants crystal
Issue Date:	2005
Publisher:	PERGAMON-ELSEVIER SCIENCE LTD
Citation:	TETRAHEDRON LETTERS, 46(4), 665-669
Abstract:	Reactions of in situ prepared SeCl2 With Grignard reagents (prepared from bromobenzene, o-tolyl bromide, 2,6-dimethyl-4-tert-butyl-l-bromobenzene, and 1-bromo-2-methylnaphthalene) and dilithiated benzamides (prepared from N-phenyl, N-cyclohexyl, and N-isopropyl benzamide) are described. (C) 2004
URI:	http://dx.doi.org/10.1016/j.tetlet.2004.11.125 http://dspace.library.iitb.ac.in/xmlui/handle/10054/11439 http://hdl.handle.net/10054/11439
ISSN:	0040-4039
Appears in Collections:	Article

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