Diastereoselective and Branched-Aldehyde-Selective Tandem Hydroformylation–Hemiaminal Formation: Synthesis of Functionalized Piperidines and Amino Alcohols-Reference-Cited by-同舟云学术

Diastereoselective and Branched-Aldehyde-Selective Tandem Hydroformylation–Hemiaminal Formation: Synthesis of Functionalized Piperidines and Amino Alcohols

Published:2017-05-17 Issue:11 Volume:19 Page:2845-2848
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pittaway Rachael¹,Fuentes José A.¹,Clarke Matthew L.¹^ORCID

Affiliation:

1. School of Chemistry, University of St Andrews, Purdie Building, North Haugh, St Andrews, Fife KY16 9ST, United Kingdom

Funder

Engineering and Physical Sciences Research Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01049

Reference60 articles.

1. avan Leeuwen, P. W. N. M.; Claver, C.Rhodium Catalyzed Hydroformylation.James, B. R., van Leeuwen, P. W. N. M., Ed.Kluwer Academic Publishers, 2000; p22.

2. Applied Hydroformylation

3. Hydroformylation

4. Diphosphines with natural bite angles near 120.degree. increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation

5. New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle

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