dc.contributor.author |
Swamy, V. S. V. S. N. |
en_US |
dc.contributor.author |
PARVIN, NASRINA |
en_US |
dc.contributor.author |
Raj, K. Vipin |
en_US |
dc.contributor.author |
Vanka, Kumar |
en_US |
dc.contributor.author |
Sen, Sakya S. |
en_US |
dc.date.accessioned |
2019-07-01T05:35:43Z |
|
dc.date.available |
2019-07-01T05:35:43Z |
|
dc.date.issued |
2017-08 |
en_US |
dc.identifier.citation |
Chemical Communications, 53(71),9850-9853. |
en_US |
dc.identifier.issn |
1359-7345 |
en_US |
dc.identifier.issn |
1364-548X |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3286 |
|
dc.identifier.uri |
https://doi.org/10.1039/C7CC05145J |
en_US |
dc.description.abstract |
Silylene [PhC(NtBu)2SiN(SiMe3)2] (1) cleaves the C(sp3)–H and C–F bonds of acetophenone and 1,1,1-trifluoroacetophenone, respectively, under mild conditions. The reaction is initiated via a nucleophilic attack from the oxygen to the silicon atom followed by C–F/H bond cleavage. The scope of C–F bond activation has further been extended with C6F6 and C6F5CF3. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Silylene |
en_US |
dc.subject |
Nucleophilic attack |
en_US |
dc.subject |
High activation barrier |
en_US |
dc.subject |
Defluorination |
en_US |
dc.subject |
2017 |
en_US |
dc.title |
C(sp3)–F, C(sp2)–F and C(sp3)–H bond activation at silicon(ii) centers |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Chemical Communications |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |