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Donor free stibenium cation as an efficient cyanosilylation catalyst

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dc.contributor.author SEN, NILANJANA en_US
dc.contributor.author GOTHE, PRACHI en_US
dc.contributor.author Sarkar, Pallavi en_US
dc.contributor.author Das, Shubhajit en_US
dc.contributor.author Tothadi, Srinu en_US
dc.contributor.author Pati, Swapan K. en_US
dc.contributor.author KHAN, SHABANA en_US
dc.date.accessioned 2022-09-13T10:42:14Z
dc.date.available 2022-09-13T10:42:14Z
dc.date.issued 2022-09 en_US
dc.identifier.citation Chemical Communications, 58(74), 10380-10383. en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.issn 1364-548X en_US
dc.identifier.uri https://doi.org/10.1039/D2CC03158B en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7355
dc.description.abstract The synthesis of novel stibenium cations and their catalytic application in cyanosilylation of carbonyl compounds have been described. Treatment of chlorostibine L1SbCl [L1 = 1,2-C6H4{N(CH2tBu)}2] (2) with 1 equiv. of AgOTf and AgSbF6 resulted in the formation of donor free L1SbOTf (3) and [L1Sb]+[SbF6]− (4), respectively. Among these three compounds, 4 exhibits excellent catalytic activity towards the cyanosilylation of aldehydes and ketones. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Pnictogenium Cations en_US
dc.subject Lewis Acidity en_US
dc.subject Hydroboration en_US
dc.subject Activation en_US
dc.subject Hydrosilylation en_US
dc.subject Chemistry en_US
dc.subject Germylene en_US
dc.subject Antimony en_US
dc.subject Complex en_US
dc.subject 2022-SEP-WEEK1 en_US
dc.subject TOC-SEP-2022 en_US
dc.subject 2022 en_US
dc.title Donor free stibenium cation as an efficient cyanosilylation catalyst 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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