Copper-catalyzed dehydrogenative borylation of terminal alkynes with pinacolborane
Author:
Affiliation:
1. UCSD-CNRS Joint Research Chemistry Laboratory (UMI 3555)
2. Department of Chemistry and Biochemistry
3. University of California San Diego
4. La Jolla
5. USA
Abstract
LCuOTf complexes (L = CAACs or NHCs) selectively promote the dehydrogenative borylation of C(sp)–H bonds at room temperature.
Funder
Office of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/SC/C6SC02668K
Reference43 articles.
1. Borylation and Silylation of C–H Bonds: A Platform for Diverse C–H Bond Functionalizations
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3. Thermal, Catalytic, Regiospecific Functionalization of Alkanes
4. Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds
5. Regioselectivity of the borylation of alkanes and arenes
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