Asymmetric Direct Aldol Reactions Catalyzed by a Simple Chiral Primary Diamine–Br⊘nsted Acid Catalyst in/on Water-Reference-Cited by-同舟云学术

Asymmetric Direct Aldol Reactions Catalyzed by a Simple Chiral Primary Diamine–Br⊘nsted Acid Catalyst in/on Water

Published:2009-01-29 Issue:5 Volume:39 Page:764-774
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Li Li¹,Xu Li-Wen¹²,Ju Ya-Dong¹,Lai Guo-Qiao¹

Affiliation:

1. a Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Educations, College of Chemistry and Chemical Engineering, Hangzhou Normal University , Hangzhou, China

2. b State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences , Lanzhou, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910802431131

Reference13 articles.

1. Enzymes in organic synthesis: recent developments in aldol reactions and glycosylations

2. Diastereoselection in Lewis-Acid-Mediated Aldol Additions

3. Proline-Catalyzed Direct Asymmetric Aldol Reactions

4. The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysts

5. Polymer-Supported Organic Catalysts

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