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http://nopr.niscpr.res.in/handle/123456789/41549Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Gupta, B D | - |
| dc.contributor.author | Das, Indira | - |
| dc.date.accessioned | 2017-05-01T05:48:31Z | - |
| dc.date.available | 2017-05-01T05:48:31Z | - |
| dc.date.issued | 1996-12 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/41549 | - |
| dc.description | 1111-1113 | en_US |
| dc.description.abstract | Several allyl (both cyclic and acyclic), allenyl, hexenyl and propargylcobaloximes react regiospecifically with thiophone-2-sulphonyl chloride under thermal and photochemical conditions to give the corresponding sulphones. The reaction is believed to take place by the attack of the sulphur radical on the terminal carbon of the organocobaloxime with the displacement of cobaloxime(II). | 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.35A(12) [December 1996] | en_US |
| dc.title | Homolytic displacement at carbon in organocobaloximes: Part 9†-Reactions of organocobaloximes with thiophene 2-sul-phonylchloride | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.35A(12) [December 1996] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 35A(12) 1111-1113.pdf | 462.32 kB | Adobe PDF | View/Open |
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