Selectively Tunable Synthesis of α-Trifluoromethyl Ketones-Reference-Cited by-同舟云学术

Selectively Tunable Synthesis of α-Trifluoromethyl Ketones

Published:2023-03-23 Issue:13 Volume:25 Page:2344-2348
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhou Pan¹,Lu Shanya¹,Wu Xiaoqiang¹,Zhong Wei²^ORCID,XU Tao¹^ORCID

Affiliation:

1. Shanghai Key Laboratory of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, 1239 Siping Road, Shanghai, 200092, P. R. of China

2. College of Biological, Chemical Sciences and Engineering, Jiaxing University, 118 Jiahang Road, Jiaxing, 314001, P. R. of China

Funder

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c00725

Reference36 articles.

1. Organic fluorine compounds: a great opportunity for enhanced materials properties

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

3. Catalytic Asymmetric Synthesis of Enantioenriched Heterocycles Bearing a CCF3Stereogenic Center

4. Recent advances in transition metal-mediated trifluoromethylation reactions

5. Electrophilic Trifluoromethylation by Use of Hypervalent Iodine Reagents

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