Ru-Catalyzed Asymmetric Reductive Amination of Aryl-Trifluoromethyl Ketones for Synthesis of Primary α-(Trifluoromethyl)arylmethylamines-Reference-Cited by-同舟云学术

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Ru-Catalyzed Asymmetric Reductive Amination of Aryl-Trifluoromethyl Ketones for Synthesis of Primary α-(Trifluoromethyl)arylmethylamines

Published:2023-07-03 Issue:27 Volume:25 Page:5033-5037
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Yuan-Zheng¹,Hu Le’an¹,Bai Shao-Tao¹²^ORCID,Zhang Xumu¹^ORCID

Affiliation:

1. Department of Chemistry and Shenzhen Key Laboratory of Small Molecule Drug Discovery and Synthesis, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen 518055, China

2. Institute of Carbon-Neutral Technology and Center for Carbon-Neutrality Catalysis and Engineering, Shenzhen Polytechnic, No. 7098 Liuxian Avenue, Nanshan District, Shenzhen 518055, China

Funder

National Key Research and Development Program of China

Basic and Applied Basic Research Foundation of Guangdong Province

Shenzhen Polytechnic

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01734

Reference41 articles.

1. Solution/solid-phase synthesis of partially modified retro- ψ [NHCH(CF 3 )]-peptidyl hydroxamates

2. Stereocontrolled Synthesis of ψ[CH(CF3)NH]Gly-Peptides

3. The Trifluoroethylamine Function as Peptide Bond Replacement

4. Asymmetric Construction of Stereogenic Carbon Centers Featuring a Trifluoromethyl Group from Prochiral Trifluoromethylated Substrates

5. Advances in Catalytic Enantioselective Fluorination, Mono-, Di-, and Trifluoromethylation, and Trifluoromethylthiolation Reactions

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