Synthesis of Α,β-Unsaturated Ketones by Rhodium-Catalyzed Carbonylative Arylation of Internal Alkynes With Arylboronic Acids
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BRONZE
Green Open Access
Yes
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No
Abstract
The Rh-catalyzed reaction of arylboronic acids with internal alkynes under a CO atmosphere in the presence of an acid additive afforded α,β-unsaturated ketones as the major products. Hydroacylation of internal alkynes, except in the case of diaryl acetylenes, proceeded in syn fashion, yielding the E-configured isomer. A mixture of E- and Z-isomers was obtained with diphenyl acetylene. Reactions were also highly regioselective for various nonsymmetric alkynes.
Description
Keywords
Alkynes, Boron, Carbonylation, Enones, Rhodium, Alkynes, Enones, Carbonylation, Rhodium, Boron
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
Kuş, M., Aksın Artok, Ö., Ziyanak, F., and Artok, L. (2008). Synthesis of α,β-unsaturated ketones by rhodium-catalyzed carbonylative arylation of internal alkynes with arylboronic acids. Synlett, (17), 2587-2592.
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OpenCitations Citation Count
2
Source
Volume
2008
Issue
17
Start Page
2587
End Page
2592
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