Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/44091Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Gupta, B D | - |
| dc.contributor.author | Das, Indira | - |
| dc.contributor.author | Dixit, Vandana | - |
| dc.date.accessioned | 2018-03-26T09:04:09Z | - |
| dc.date.available | 2018-03-26T09:04:09Z | - |
| dc.date.issued | 1993-12 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/44091 | - |
| dc.description | 1019-1022 | en_US |
| dc.description.abstract | The reactions of but-3-enyl cobaloximes with thiophene-2-sulphonyl chloride under thermal and photochemical conditions give the corresponding cyclopropylmethyl sulphones. A similar reaction with cyclopent-2-enylmethyl and cyclohex-2-enylmethyl cobaloximes gives a mixture of cis- and trans- bicyclic products. Cycloalkane, spirocycloprop-2-yl sulphone is formed exclusively from the reaction of 2-(cycloalk-1-enyl)ethyl cobaloxime. The reactions are interpreted in terms of SH 2 mechanism. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.32A(12) [December 1993] | en_US |
| dc.title | Homolytic displacement at saturated carbon: Part 7†-Synthesis of cyclic, bicyclic and spirocyclic sulphones from the corresponding butenyl cobaloximes with thiophene- 2-sulphonyl chloride | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.32A(12) [December 1993] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 32A(12) 1019-1022.pdf | 257.7 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.