Diastereo- and Enantioselective anti-Alkoxyallylation Employing Allylic gem-Dicarboxylates as Allyl Donors via Iridium-Catalyzed Transfer Hydrogenation-Reference-Cited by-同舟云学术

Diastereo- and Enantioselective anti-Alkoxyallylation Employing Allylic gem-Dicarboxylates as Allyl Donors via Iridium-Catalyzed Transfer Hydrogenation

Published:2010-01-25 Issue:6 Volume:132 Page:1760-1761
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Han Soo Bong¹,Han Hoon¹,Krische Michael J.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, Texas 78712

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9097675

Reference48 articles.

1. Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones

2. Regulation of Stereoselectivity and Reactivity in the Inter- and Intramolecular Allylic Transfer Reactions

3. Creation of quaternary stereocenters in carbonyl allylation reactions

4. Lewis and Brønsted Acid Catalyzed Allylboration of Carbonyl Compounds: From Discovery to Mechanism and Applications

5. α-Hydroxyallylation Reaction of Carbonyl Compounds

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