dc.contributor.author |
MAJUMDAR, MOUMITA |
en_US |
dc.contributor.author |
RAUT, RAVINDRA K. |
en_US |
dc.contributor.author |
SAHOO, PADMINI |
en_US |
dc.contributor.author |
Kumar, Vikas |
en_US |
dc.date.accessioned |
2018-10-12T05:13:33Z |
|
dc.date.available |
2018-10-12T05:13:33Z |
|
dc.date.issued |
2018-10 |
en_US |
dc.identifier.citation |
Chemical Communications. Vol. 54(77). |
en_US |
dc.identifier.issn |
1364-548X |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1298 |
|
dc.identifier.uri |
https://doi.org/10.1039/c8cc06067c |
en_US |
dc.description.abstract |
Bis(chlorogermyliumylidene) 2 has been strategically obtained within redox-active bis(-iminopyridine). Metal-free reduction of 2 followed by protonation led to elusive 2,3-di(pyridin-2-yl)piperazine with meso-stereoselectivity. Formation of persistent triplet diradicals upon reduction and isolation of piperazine stabilized Ge(ii) dication intermediates provide convincing evidence for the crucial role of [GeCl](+) units in reductive cyclization. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Chiral Piperazines |
en_US |
dc.subject |
Transition-Metals |
en_US |
dc.subject |
Radical Reactions |
en_US |
dc.subject |
Chemistry |
en_US |
dc.subject |
Coordination |
en_US |
dc.subject |
Germylene |
en_US |
dc.subject |
Dication |
en_US |
dc.subject |
State |
en_US |
dc.subject |
Germyliumylidene |
en_US |
dc.subject |
Diradicals |
en_US |
dc.subject |
TOC-OCT-2018 |
en_US |
dc.subject |
2018 |
en_US |
dc.title |
Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization |
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 |