Title of article
Reactions of organocobaloximes with aryldisulfonyl chlorides
Author/Authors
B.D. Gupta، نويسنده , , V. Vijaikanth، نويسنده ,
Issue Information
دوفصلنامه با شماره پیاپی سال 2004
Pages
8
From page
1102
To page
1109
Abstract
Photochemical reactions of benzyl, heteroaromaticmethyl and allylcobaloximes with aryldisulfonyl chlorides yield symmetrical disulfones. Allyl cobaloximes yield allyldisulfones as the major product whereas bibenzyl is the major product in benzylcobaloximes. A time dependent 1H NMR studies show that bibenzyl is formed from O-benzyldimethylglyoxime – a predominant product in the initial stage of the reaction.
Keywords
Organocobaloximes , Disulfonyl chlorides , 1H NMR studies , Bibenzyl-O-benzyldimethylglyoxime , Disulfone , SH2 reactions
Journal title
Journal of Organometallic Chemistry
Serial Year
2004
Journal title
Journal of Organometallic Chemistry
Record number
1376750
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