Mannich-Type Reaction of α-Sulfanyl N-tert-Butanesulfinylimidates: Diastereoselective Access to α-Mercapto-β-amino Acid Derivatives-Reference-Cited by-同舟云学术

Mannich-Type Reaction of α-Sulfanyl N-tert-Butanesulfinylimidates: Diastereoselective Access to α-Mercapto-β-amino Acid Derivatives

Published:2021-01-28 Issue:3 Volume:86 Page:3049-3058
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Feng Jie¹²,Liu Hui¹,Yao Yun³,Lu Chong-Dao³^ORCID

Affiliation:

1. Key Laboratory of Plant Resources and Chemistry of Arid Zones, Xinjiang Technical Institute of Physics & Chemistry, Chinese Academy of Sciences, Urumqi 830011, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

3. School of Chemical Science and Technology, Yunnan University, Kunming 650091, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02583

Reference53 articles.

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2. Investigation of Subsite Preferences in Aminopeptidase A (EC 3.4.11.7) Led to the Design of the First Highly Potent and Selective Inhibitors of This Enzyme

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4. Development of Potent Inhibitors of Botulinum Neurotoxin Type B

5. Thio-derived disulfides as potent inhibitors of botulinum neurotoxin type B: implications for zinc interaction

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