Regioselective 1,2-Alkoxy and Hydroxy Iodination of Alkenes by 1,4-Dibenzyl-1,4-Diazabicyclo[2.2.2]Octane Dichloroiodate

Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/66167

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DC Field	Value	Language
dc.contributor.author	Mohammad Alikarami	en_US
dc.contributor.author	Somaye Mohammadnezhad	en_US
dc.contributor.author	Zahra Abbasi	en_US
dc.date.accessioned	2019-08-21T09:18:23Z	-
dc.date.available	2019-08-21T09:18:23Z	-
dc.date.issued	2015	en_US
dc.identifier.citation	Chiang Mai Journal of Science 42, 4 (Oct 2015), 957 - 962	en_US
dc.identifier.issn	0125-2526	en_US
dc.identifier.uri	http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=6250	en_US
dc.identifier.uri	http://cmuir.cmu.ac.th/jspui/handle/6653943832/66167	-
dc.description.abstract	The reaction of 1,4-dibenzyl-1,4-diabicyclo [2.2.2] octane dichloroiodate (DBDDCI) with alkenes in the presence of oxygenated nucleophilic solvents (alcohols or H2O/CH3CN (1:1)) in mild and under catalyst free condition at room temperature led to the corresponding β-iodoethers and iodohydrines in good to excellent yield.	en_US
dc.language.iso	Eng	en_US
dc.publisher	Science Faculty of Chiang Mai University	en_US
dc.subject	1,4-dibenzyl-1	en_US
dc.subject	4-diazabicyclo[2.2.2]octane dichloroiodate	en_US
dc.subject	co-iodination	en_US
dc.subject	iodohydrines	en_US
dc.subject	β-iodoether	en_US
dc.subject	catalyst free	en_US
dc.title	Regioselective 1,2-Alkoxy and Hydroxy Iodination of Alkenes by 1,4-Dibenzyl-1,4-Diazabicyclo[2.2.2]Octane Dichloroiodate	en_US
Appears in Collections:	CMUL: Journal Articles

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