Cu-catalyzed direct C1–H trifluoromethylation of pyrrolo[1,2-a]quinoxalines-Reference-Cited by-同舟云学术

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Cu-catalyzed direct C1–H trifluoromethylation of pyrrolo[1,2-a]quinoxalines

Published:2022-01 Issue: Volume:105 Page:132610
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Li Yang,Liu Yali,Hao Di,Li Chuntian,Liu Yan,Gu Yanlong,Vaccaro Luigi,Liu Ping

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference80 articles.

1. Fluorine in medicinal chemistry

2. Catalysis for fluorination and trifluoromethylation

3. Amide Bond Bioisosteres: Strategies, Synthesis, and Successes

4. Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K

5. Fluorine and Fluorinated Motifs in the Design and Application of Bioisosteres for Drug Design

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1. Recent Advances in Trifluoromethylation of Olefins, Aldehydes, and Ketones;Current Organic Chemistry;2024-09

2. Transition‐Metal‐Free (Hetero)arylsulfonylation of 1‐Iodopyrrolo[1,2‐a]quinoxalines;ChemistrySelect;2024-07-10

3. C1 − H morpholinomethylation and formylation of pyrrolo[1,2- a ]quinoxalines;Synthetic Communications;2024-06-09

4. Synthesis of 1-arylsulfonyl pyrrolo[1,2-a]quinoxalines: Scope and limitation;Tetrahedron Letters;2023-09

5. K2S2O8-promoted C3-thiocyanation of pyrazole [1,5-a] pyrimidine-7-amines;Tetrahedron;2023-04

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