Please use this identifier to cite or link to this item:
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2103
Title: | A 1,3-amino group migration route to form acrylamidines |
Authors: | Chauhan, Dinesh Pratapsinh Varma, Sreejith Jayasree Vijeta, Arjun BANERJEE, PALLAVI TALUKDAR, PINAKI Dept. of Chemistry |
Keywords: | A 1,3-amino group migration Acrylamidines Bioconjugation Instantaneously participates 2013 |
Issue Date: | Oct-2013 |
Publisher: | Royal Society of Chemistry |
Citation: | Chemical Communications, 50(3), 323-325. |
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. |
URI: | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2103 https://doi.org/10.1039/C3CC47182A |
ISSN: | 1359-7345 1364-548X |
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.