Rhodium Catalysed Chemo- and Stereoselective Arylative and Alkenylative Cyclisation Reactions of Unsymmetric Diynes Containing a Terminal Alkyne Moiety With Organoboronic Acids
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Open Access Color
BRONZE
Green Open Access
Yes
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7
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2
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No
Abstract
Unsymmetric diynes possessing a terminal alkyne moiety reacted with organoboronic acids both chemo- and stereoselectively to afford arylated or alkenylated exocyclic dienes by catalysis from the [Rh(cod)OCH 3] 2 complex. The use of a polar protic solvent, e.g. CH 3OH is required for the success of the process under mild conditions. © 2010 The Royal Society of Chemistry.
Description
Keywords
Rhodium, Cyclisations, Organoboronic acids, Protic solvents, Terminal alkyne, Cyclisations, Molecular Structure, Organoboronic acids, Esters, Stereoisomerism, Terminal alkyne, Boronic Acids, Protic solvents, Catalysis, Alkadienes, Cyclization, Alkynes, Organometallic Compounds, Rhodium
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
Artok, L., Kuş, M., Ürer, B. N., Türkmen, G., and Aksın Artok, Ö. (2010). Rhodium catalysed chemo- and stereoselective arylative and alkenylative cyclisation reactions of unsymmetric diynes containing a terminal alkyne moiety with organoboronic acids. Organic and Biomolecular Chemistry, 8(9), 2060-2067. doi:10.1039/b926553h
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OpenCitations Citation Count
16
Volume
8
Issue
9
Start Page
2060
End Page
2067
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CrossRef : 16
Scopus : 14
PubMed : 1
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