Synlett
DOI: 10.1055/a-2508-4824
account

Straightforward synthesis of unnatural α,α-disubstituted α-amino acid derivatives using readily accessible building blocks

1   Faculty of Pharmaceutical Sciences, Kyoto Pharmaceutical University, Kyoto, Japan (Ringgold ID: RIN12916)
,
Takeru Nose
2   Faculty of Arts and Science, Kyushu University, Fukuoka, Japan (Ringgold ID: RIN12923)
,
Hisanori Nambu
3   Pharmaceutical Manufacturing Chemistry, Kyoto Pharmaceutical University, Kyoto, Japan (Ringgold ID: RIN12916)
› Author Affiliations
Supported by: Society of Synthetic Organic Chemistry
Supported by: Ube Foundation
Supported by: Kanamori Foundation
Supported by: JSPS KAKENHI JP26870217, JP17K17750, JP21K05290
Supported by: TOBE MAKI Scholarship Foundation
Supported by: JST Adaptable and Seamless Technology transfer Program through Target-driven R&D (A-STEP) JPMJTM22EA
Supported by: Tamura Science and Technology Foundation

Unnatural α,α-disubstituted α-amino acids have played a privileged role in drug discovery campaign, and the development of their efficient synthetic methods has thus received continuous attention. This review describes our originally developed synthetic methods of α,α-disubstituted α-amino acid derivatives using readily accessible building blocks. 1 Introduction 2 Asymmetric synthesis of α,α-disubstituted α-aryl α-amino acid derivatives from L-α-amino acids via “Memory of Chirality” 3 Synthesis of natural product-derived α,α-disubstituted α-amino acid derivatives by chemical engineering of natural product extracts 4 One-pot synthesis of α,α-disubstituted α-amino acid derivatives by ammonia-Ugi reaction



Publication History

Received: 22 November 2024

Accepted after revision: 27 December 2024

Accepted Manuscript online:
27 December 2024

© . Thieme. All rights reserved.

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany