The synthetic versatility of fluoroiodomethane: recent applications as monofluoromethylation platform-Reference-Cited by-同舟云学术

The synthetic versatility of fluoroiodomethane: recent applications as monofluoromethylation platform

Published:2022 Issue:23 Volume:20 Page:4669-4680
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Colella Marco¹^ORCID,Musci Pantaleo¹,Andresini Michael¹^ORCID,Spennacchio Mauro¹,Degennaro Leonardo¹^ORCID,Luisi Renzo¹^ORCID

Affiliation:

1. FLAME-Lab, Flow Chemistry and Microreactor Technology Laboratory, Department of Pharmacy – Drug Sciences, University of Bari “A. Moro” Via E. Orabona 4, 70125 Bari, Italy

Abstract

This minireview covers the recent relevant literature updates on the use of CH2FI as readily available platform for monofluoromethylation strategies.

Funder

Universita degli Studi di Bari Aldo Moro

Ministero dell'Università e della Ricerca

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00670G

Reference78 articles.

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

2. Introduction of Fluorine and Fluorine-Containing Functional Groups

3. Good Partnership between Sulfur and Fluorine: Sulfur-Based Fluorination and Fluoroalkylation Reagents for Organic Synthesis

4. Fluorinated Carbonyl and Olefinic Compounds: Basic Character and Asymmetric Catalytic Reactions

5. Electrophilic Trifluoromethylation by Use of Hypervalent Iodine Reagents

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