2,3-Difunctionalization of quinones: a gold-catalyzed cascade approach for trifluoromethyl-amination or sulfoximination-Reference-Cited by-同舟云学术

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2,3-Difunctionalization of quinones: a gold-catalyzed cascade approach for trifluoromethyl-amination or sulfoximination

Published:2024 Issue:71 Volume:60 Page:9598-9601
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Sharma Alpa¹²,Govande Vijaya¹,Mahajan Shivangani¹²,Sawant Sanghapal D.¹³²^ORCID

Affiliation:

1. Natural Products and Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu-180001, India

2. Academy of Scientific and Industrial Research, Ghaziabad-201002, India

3. Organic Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune-411008, India

Abstract

A one-pot domino protocol employing gold(i) catalysis has been developed for the cascade trifluoromethyl-amination/sulfoximination of quinones.

Funder

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC01891E

Reference20 articles.

1. Drug specific, tuning of an ionic liquid's hydrophilic–lipophilic balance to improve water solubility of poorly soluble active pharmaceutical ingredients

2. Contribution of Organofluorine Compounds to Pharmaceuticals

3. Quinone-Based Drugs: An Important Class of Molecules in Medicinal Chemistry

4. Visible light–initiated radical 1,3-difunctionalization of β,γ-unsaturated ketones

5. Copper-mediated C–H trifluoromethylation of quinones

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