Electronically Dissymmetric DIPHOS Derivatives Give Higher n:i Regioselectivity in Rhodium-Catalyzed Hydroformylation Than Either of Their Symmetric Counterparts-Reference-Cited by-同舟云学术

Electronically Dissymmetric DIPHOS Derivatives Give Higher n:i Regioselectivity in Rhodium-Catalyzed Hydroformylation Than Either of Their Symmetric Counterparts

Published:1998-12-19 Issue:1 Volume:121 Page:63-70
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Casey Charles P.¹,Paulsen Evelyn Lin¹,Beuttenmueller Eckart W.¹,Proft Bernd R.¹,Matter Brock A.¹,Powell Douglas R.¹

Affiliation:

1. Contribution from the Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53706

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja982117h

Reference40 articles.

1. (a) Parshall, G. W.Homogeneous Catalysis: The Applications and Chemistry ofCatalysis by Soluble Transition Metal Complexes; Wiley: New York, 1980.

2. (c) Tolman, C. A.; Faller, J. W. InHomogeneous Catalysis withMetal Phosphine Complexes; Pignolet, L. H., Ed.; Plenum: New York, 1983; pp 81−109.

3. (d) Pino, P.; Piacenti, F.; Bianchi, M. InOrganic Syntheses viaMetal Carbonyls; Wender, I., Pino, P., Eds.; Wiley-Interscience: New York, 1977; Vol. 2, pp 136−197.

4. Asymmetric hydroformylation

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