Please use this identifier to cite or link to this item:
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2719
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Manoharan, Ramasamy | en_US |
dc.contributor.author | JAYAKANNAN, MANICKAM | en_US |
dc.date.accessioned | 2019-04-29T10:15:50Z | |
dc.date.available | 2019-04-29T10:15:50Z | |
dc.date.issued | 2016-08 | en_US |
dc.identifier.citation | European Journal of Organic Chemistry, 2016(23), 4013-4019. | en_US |
dc.identifier.issn | 1434-193X | en_US |
dc.identifier.issn | 1099-0690 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2719 | - |
dc.identifier.uri | https://doi.org/10.1002/ejoc.201600505 | en_US |
dc.description.abstract | A highly regioselective ruthenium‐catalyzed C–H amidation of cyclic N‐sulfonyl ketimines with organic sulfonyl azides is described. An alkenylation at the C–H bond of cyclic N‐sulfonyl ketimines with various alkenes was also carried out. Only a catalytic amount of the oxidant Cu(OAc)2 was used in the reaction; the remainder of the required amount of oxidant was formed by regeneration of Cu(OAc)2 under an air atmosphere. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Ruthenium?Catalyzed | en_US |
dc.subject | C-H Amidation | en_US |
dc.subject | Alkenylation | en_US |
dc.subject | Cyclic N?Sulfonyl Ketimines | en_US |
dc.subject | Heteroaromatic compound | en_US |
dc.subject | 2016 | en_US |
dc.title | Ruthenium‐Catalyzed C–H Amidation and Alkenylation of Cyclic N‐Sulfonyl Ketimines | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | European Journal of Organic Chemistry | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.