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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BRONZE

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Yes

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7

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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.

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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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16

Volume

8

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9

Start Page

2060

End Page

2067
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Scopus : 14

PubMed : 1

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Mendeley Readers : 7

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