A 1,3-amino group migration route to form acrylamidines

Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2103

Full metadata record

DC Field	Value	Language
dc.contributor.author	Chauhan, Dinesh Pratapsinh	en_US
dc.contributor.author	Varma, Sreejith Jayasree	en_US
dc.contributor.author	Vijeta, Arjun	en_US
dc.contributor.author	BANERJEE, PALLAVI	en_US
dc.contributor.author	TALUKDAR, PINAKI	en_US
dc.date.accessioned	2019-02-25T09:26:08Z
dc.date.available	2019-02-25T09:26:08Z
dc.date.issued	2013-10	en_US
dc.identifier.citation	Chemical Communications, 50(3), 323-325.	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/123456789/2103	-
dc.identifier.uri	https://doi.org/10.1039/C3CC47182A	en_US
dc.description.abstract	A novel 1,3-amino group migration strategy for the synthesis of acrylamidines is presented. Cu(I) catalyzed reaction of N,N-disubstituted propargylamine with tosylazide generates a highly reactive ketenimine intermediate which is trapped by a tethered amino group leading to the rearrangement reaction.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	A 1,3-amino group migration	en_US
dc.subject	Acrylamidines	en_US
dc.subject	Bioconjugation	en_US
dc.subject	Instantaneously participates	en_US
dc.subject	2013	en_US
dc.title	A 1,3-amino group migration route to form acrylamidines	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
Appears in Collections:	JOURNAL ARTICLES

Files in This Item:

There are no files associated with this item.