An efficient enantioselective synthesis of (S)-α-methyl-serine methyl ester hydrochloride via asymmetrically catalyzed amination-Reference-Cited by-同舟云学术

An efficient enantioselective synthesis of (S)-α-methyl-serine methyl ester hydrochloride via asymmetrically catalyzed amination

Published:2019-07-16 Issue:1 Volume:22 Page:61-68
ISSN:1028-6020
Container-title:Journal of Asian Natural Products Research
language:en
Short-container-title:Journal of Asian Natural Products Research

Author:

Xiao Qiong¹,Tang Yi-Fan²,Xie Ping¹

Affiliation:

1. Department of Medicinal Chemistry, Beijing Key Laboratory of Active Substances Discovery and Druggability Evaluation & State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100050, China;

2. Department of Synthetic Medicinal Chemistry, Beijing Union Pharmaceutical Factory, Beijing 102600, China

Funder

Drug Innovation Major Project

National Key R&D Program of China

CAMS Innovation Fund for Medical Sciences

Publisher

Informa UK Limited

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10286020.2019.1634058

Reference16 articles.

1. Recent developments in the stereoselective synthesis of α-aminoacids

2. Peptidomimetics—Tailored Enzyme Inhibitors

3. New Strategies toα-Alkylatedα-Amino Acids

4. Solvent Effects on the 310-/α-Helix Equilibrium in Short Amphipathic Peptides Rich in α,α-Disubstituted Amino Acids

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