Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/66167
Title: Regioselective 1,2-Alkoxy and Hydroxy Iodination of Alkenes by 1,4-Dibenzyl-1,4-Diazabicyclo[2.2.2]Octane Dichloroiodate
Authors: Mohammad Alikarami
Somaye Mohammadnezhad
Zahra Abbasi
Authors: Mohammad Alikarami
Somaye Mohammadnezhad
Zahra Abbasi
Keywords: 1,4-dibenzyl-1;4-diazabicyclo[2.2.2]octane dichloroiodate;co-iodination;iodohydrines;β-iodoether;catalyst free
Issue Date: 2015
Publisher: Science Faculty of Chiang Mai University
Citation: Chiang Mai Journal of Science 42, 4 (Oct 2015), 957 - 962
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.
URI: http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=6250
http://cmuir.cmu.ac.th/jspui/handle/6653943832/66167
ISSN: 0125-2526
Appears in Collections:CMUL: Journal Articles

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