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Bis(chlorogermyliumylidene) and its significant role in elusive reductive cyclization

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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


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