Accessing unnatural α-amino acids with tetrasubstituted stereogenic centers<i>via</i>catalytic enantioselective reactions of ketimine-type α-iminoesters/α-iminoamides-Reference-Cited by-同舟云学术

Accessing unnatural α-amino acids with tetrasubstituted stereogenic centersviacatalytic enantioselective reactions of ketimine-type α-iminoesters/α-iminoamides

Published:2023 Issue:54 Volume:59 Page:8343-8374
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yasukawa Naoki¹^ORCID,Nakamura Shuichi¹^ORCID

Affiliation:

1. Department of Life Science and Applied Chemistry, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

Abstract

Feature article on catalytic enantioselective reactions of ketimine-type α-iminoesters with the aim of accessing unnatural α-tertiary amino acids (ATAAs), which are highly valuable chemical molecules for natural products and functional materials.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC02236F

Reference204 articles.

1. Probing Protein Structure and Function with an Expanded Genetic Code

2. Expanding the Genetic Code

3. Unusual Amino Acids in Medicinal Chemistry

4. Organocatalysts Derived from Unnatural α-Amino Acids: Scope and Applications

5. Reprogramming natural proteins using unnatural amino acids

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