(IPr)CuF-catalyzed α-site regiocontrolled trans-hydrofluorination of ynamides
Author:
Affiliation:
1. Department of Applied Chemistry
2. College of Chemistry and Molecular Engineering
3. Nanjing Tech University
4. Nanjing 211816
5. People’ s Republic of China
Abstract
Experimental results indicate that the regioselectivity of the reaction is unexpectedly opposite to observed in the (Ph3P)3CuF-catalyzed hydrofluorination of ynamides, and the resulting α-fluoro products allowed for the synthesis of α-fluoro imides through further transformations.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01345G
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