Formal hydrogenation of arynes with silyl Cβ–H bonds as an active hydride source
Author:
Affiliation:
1. Department of Chemistry
2. University of Illinois at Chicago
3. Chicago, USA
4. College of Chemistry and Materials Engineering
5. Wenzhou University
6. , P. R. China
Abstract
In stark contrast to the effective 1°, 2°, and 3° C–H bond insertion of alkyl groups tethered to arynes, the 2° and 3° C–H bonds on the β-carbon of silyl groups show high tendency for hydride transfer rather than C–H insertion, whereas the corresponding 1° C–H bonds exclusively undergo C–H insertion.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/SC/C3SC53478B
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4. The Direct Acyl-Alkylation of Arynes
5. Synthesis of Xanthones, Thioxanthones, and Acridones by the Coupling of Arynes and Substituted Benzoates
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