CSIR Central

Homolytic displacement at saturated carbon in organocobaloximes: Part VI† - Synthesis of benzyl sulphones

IR@NISCAIR: CSIR-NISCAIR, New Delhi - ONLINE PERIODICALS REPOSITORY (NOPR)

View Archive Info
 
 
Field Value
 
Title Homolytic displacement at saturated carbon in organocobaloximes: Part VI† - Synthesis of benzyl sulphones
 
Creator Gupta, B D
Das, Indira
Dixit, Yandana
 
Description 762-766
The reactions of thiophene-2-sulphonyl chloride with benzyl and <em>para</em>-substituted benzyl cobaloximes under anaerobic and photochemical conditions at 0&deg;C give benzyl sulphones and bibenzyls in variable yields. However, the reactions with heteroaromatic methyl cobaloximes give the corresponding sulphones as the exclusive organic products. The reactions are interpreted in terms of S<sub>H</sub>2 mechanism.
 
Date 2018-03-21T09:53:47Z
2018-03-21T09:53:47Z
1993-09
 
Type Article
 
Identifier 0975-0975(Online); 0376-4710(Print)
http://nopr.niscair.res.in/handle/123456789/43976
 
Language en_US
 
Rights <img src='http://nopr.niscair.res.in/image/cc-license-sml.png'> <a href='http://creativecommons.org/licenses/by-nc-nd/2.5/in' target='_blank'>CC Attribution-Noncommercial-No Derivative Works 2.5 India</a>
 
Publisher NISCAIR-CSIR, India
 
Source IJC-A Vol.32A(09) [September 1993]