Highly enantioselective aldol reaction of acetone with β,γ-unsaturated α-keto esters promoted by simple chiral primary–tertiary diamine catalysts-Reference-Cited by-同舟云学术

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Highly enantioselective aldol reaction of acetone with β,γ-unsaturated α-keto esters promoted by simple chiral primary–tertiary diamine catalysts

Published:2011 Issue:13 Volume:9 Page:4774
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Peng Lin,Wang Liang-Liang,Bai Jian-Fei,Jia Li-Na,Guo Yun-Long,Luo Xi-Ya,Wang Fei-Ying,Xu Xiao-Ying,Wang Li-Xin

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/OB/C1OB05607G

Reference59 articles.

1. Oxidation of propene and 1-butene byMethylococcus capsulatus andMethylosinus trichosporium

2. Aromatic biotransformations 2: production of novel chiral fluorinated 3,5-cyclohexadiene- -1,2-diol-1-carboxylates

3. Chemistry of dioxiranes. 12. Dioxiranes

4. Microbial Transformation Processes of Aliphatic Hydrocarbons

5. Catalytic Asymmetric Dihydroxylation

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1. Enantioselective vinylogous Mukaiyama aldol reaction of α-ketoesters under bifunctional organocatalysis;Chemical Communications;2021

2. Tripeptide-Catalyzed Direct Asymmetric Aldol Reaction of Activated Ketones;Journal of Synthetic Organic Chemistry, Japan;2020-12-01

3. New Application of β,γ-Unsaturated α-Ketoesters in Asymmetric Catalysis;Chinese Journal of Organic Chemistry;2020

4. Synthesis of Chiral Six-Membered Carbocyclic Purine Nucleosides via Organocatalytic Enantioselective [3 + 3] Annulation;Organic Letters;2018-08-23

5. An Efficient and Improved Process for the Scale-up Preparation of cis- Cyclopropanediamine Dihydrochloride;Letters in Organic Chemistry;2015-11-02

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