Issue 15, 2020
From the journal:

Organic & Biomolecular Chemistry

Catalytic enantioselective decarboxylative nucleophilic addition reactions using chiral organocatalysts

Kengo Hyodo*a  and  Shuichi Nakamura ORCID logo *b  

* Corresponding authors

a Department of Chemistry, School of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan
E-mail: hyodo@chem.kindai.ac.jp
Tel: +81-6-4307-3047

b Department of Frontier Materials, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan
E-mail: snakamur@nitech.ac.jp
Fax: +81-52-735-5245
Tel: +81-52-735-5245

Abstract

Catalytic decarboxylative reactions are attractive as biomimetic and environmentally friendly reaction processes. This review summarizes the recent results of organocatalytic enantioselective decarboxylative reactions of malonic acid half oxy- or thioesters, β-ketoacids, and related compounds from October 2013 to December 2019.

Graphical abstract: Catalytic enantioselective decarboxylative nucleophilic addition reactions using chiral organocatalysts

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Article information

DOI
https://doi.org/10.1039/D0OB00127A
Article type
Review Article
Submitted
20 Jan 2020
Accepted
19 Mas 2020
First published
20 Mas 2020

Org. Biomol. Chem., 2020,18, 2781-2792

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Catalytic enantioselective decarboxylative nucleophilic addition reactions using chiral organocatalysts

K. Hyodo and S. Nakamura, Org. Biomol. Chem., 2020, 18, 2781 DOI: 10.1039/D0OB00127A

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