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

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