Organocatalytic enantio- and diastereoselective synthesis of trifluoro-ethylamine allenoate derivatives containing axial and central chiralities-Reference-Cited by-同舟云学术

Organocatalytic enantio- and diastereoselective synthesis of trifluoro-ethylamine allenoate derivatives containing axial and central chiralities

Published:2024 Issue: Volume: Page:
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Shi Siyu¹,Gu Mengyun¹,Chen Danna²,Li Ruya³,Shen Zhiqiang¹⁴,Huang Jinqi²,Yan Wenjin¹^ORCID

Affiliation:

1. The Institute of Pharmacology, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China

2. Department of Hematology, Guangzhou First People's Hospital, Institute of Blood Transfusion and Hematology, Guangzhou Medical University, Guangzhou, Guangdong, China

3. The Affiliated Hospital of Guangdong Medical University, Guangdong, China

4. Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou Gansu, 730000, China

Abstract

An organocatalytic enantio- and diastereoselective synthesis of trifluoro-ethylamine allenoate derivatives containing axial and central chiralities has been achieved.

Funder

Natural Science Foundation of Gansu Province

National Natural Science Foundation of China

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC03297G

Reference42 articles.

1. Synthesis and Properties of Allenic Natural Products and Pharmaceuticals

2. Chiral Allene-Containing Phosphines in Asymmetric Catalysis

3. Allenes in Molecular Materials

4. Enantioselective Synthesis of Atropisomers with Multiple Stereogenic Axes

5. Highly atroposelective synthesis of nonbiaryl naphthalene-1,2-diamine N-C atropisomers through direct enantioselective C-H amination

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1. Organocatalytic enantio- and diastereoselective synthesis of trifluoro-ethylamine allenoate derivatives containing axial and central chiralities;Chemical Communications;2024