Journal article

Catalytic enantioselective intermolecular hydroacylation: rhodium-catalyzed combination of beta-S-aldehydes and 1,3-disubstituted allenes.

Abstract:: A rhodium(I) catalyst incorporating the Me-DuPhos ligand promotes enantioselective intermolecular hydroacylation between beta-S-aldehydes and 1,3-disubstituted allenes. The nonconjugated enone products are obtained in good yields and with high enantioselectivities.

Publication status:: Published

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APA Style

Osborne, J., Randell-Sly, H., Currie, G., Cowley, A., & Willis, M. (2008). Catalytic enantioselective intermolecular hydroacylation: rhodium-catalyzed combination of beta-S-aldehydes and 1,3-disubstituted allenes. Journal of the American Chemical Society, 130(51), 17232–17233.

MLA Style

Osborne, J, et al. “Catalytic Enantioselective Intermolecular Hydroacylation: Rhodium-Catalyzed Combination of Beta-S-Aldehydes and 1,3-Disubstituted Allenes.” Journal of the American Chemical Society, vol. 130, no. 51, 2008, pp. 17232–33.

Chicago Style

Osborne, J, H Randell-Sly, G Currie, A Cowley, and M Willis. 2008. “Catalytic Enantioselective Intermolecular Hydroacylation: Rhodium-Catalyzed Combination of Beta-S-Aldehydes and 1,3-Disubstituted Allenes.” Journal of the American Chemical Society 130 (51): 17232–33.
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Publisher copy:: 10.1021/ja8069133

Authors

+ Osborne, J More by this author

Role:: Author

+ Randell-Sly, H More by this author

Role:: Author

+ Currie, G More by this author

Role:: Author

+ Cowley, A More by this author

Role:: Author

+ Willis, M More by this author

Role:: Author

Journal:: Journal of the American Chemical Society More from this journal
Volume:: 130
Issue:: 51
Pages:: 17232-17233
Publication date:: 2008-12-01
DOI:: 10.1021/ja8069133
EISSN:: 1520-5126
ISSN:: 0002-7863

Language:: English
Keywords:: Models, Chemical

Rhodium

Molecular Structure

Aldehydes

Carbon

Catalysis

Alkenes

Metals

Stereoisomerism

Ligands

Temperature

Chemistry
Pubs id:: pubs:52478
UUID:: uuid:f363cfbf-dc83-4aa6-b5e7-720e60d8c343
Local pid:: pubs:52478
Source identifiers:: 52478
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_f363cfbfdc834aa6b5e7720e60d8c343

Terms of use

Copyright date:: 2008

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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