Regio- and stereospecific synthesis of DL-4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol

Aksu, Kadir; Kelebekli, Latif; Sahin, Ertan

Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2702

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DC Field	Value	Language
dc.contributor.author	Aksu, Kadir	-
dc.contributor.author	Kelebekli, Latif	-
dc.contributor.author	Sahin, Ertan	-
dc.date.accessioned	2022-08-17T07:11:25Z	-
dc.date.available	2022-08-17T07:11:25Z	-
dc.date.issued	2018	-
dc.identifier.uri	http://doi.org/10.1016/j.tetlet.2018.02.050	-
dc.identifier.uri	http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2702	-
dc.description.abstract	The regio- and stereospecific synthesis of DL-4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol is reported. Bromination of p-benzoquinone followed by reduction of the carbonyl groups with NaBH4 gave the corresponding trans-dibromodiol compound, which was reacted with sodium methoxide to produce dimethoxy conduritol-B. Regiospecific bromination of the alkene moiety furnished the desired chiro-inositol derivative. (C) 2018 Published by Elsevier Ltd.	en_US
dc.language.iso	eng	en_US
dc.publisher	PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND	en_US
dc.relation.isversionof	10.1016/j.tetlet.2018.02.050	en_US
dc.rights	info:eu-repo/semantics/openAccess	en_US
dc.subject	chiro-Inositol; Methoxy conduritol-B; Methoxy inositol; Regio- and stereospecific synthesis	en_US
dc.title	Regio- and stereospecific synthesis of DL-4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol	en_US
dc.type	article	en_US
dc.relation.journal	TETRAHEDRON LETTERS	en_US
dc.contributor.department	Ordu Üniversitesi	en_US
dc.contributor.authorID	0000-0002-6242-2589	en_US
dc.identifier.volume	59	en_US
dc.identifier.issue	13	en_US
dc.identifier.startpage	1258	en_US
dc.identifier.endpage	1260	en_US
Appears in Collections:	Kimya

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