Methylsulfenylation of Electrophilic Carbon Atoms: Reaction Development, Scope, and Mechanism-Reference-Cited by-同舟云学术

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Methylsulfenylation of Electrophilic Carbon Atoms: Reaction Development, Scope, and Mechanism

Published:2017-01-27 Issue:12 Volume:2017 Page:1578-1582
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Pereira Adriane A.¹,Pereira Amanda S.¹,de Mello Amanda C.¹,Carpanez Arthur G.¹,Horta Bruno A. C.²,Amarante Giovanni W.¹

Affiliation:

1. Chemistry Department; Federal University of Juiz de Fora, Cidade Universitária; 36036-900 São Pedro, Juiz de Fora Brazil

2. Chemistry Institute; Federal University of Rio de Janeiro; Cidade Universitária, CT Centro de Tecnologia; 21941-909 Rio de Janeiro Brazil

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference74 articles.

1. Catalyst-Free Insertion of Sulfoxonium Ylides into Aryl Thiols. A Direct Preparation of β-Keto Thioethers

2. Batch and Flow Synthesis of Disulfides by Visible-Light-Induced TiO2Photocatalysis

3. Copper(I)-Catalyzed Interrupted Click Reaction: Synthesis of Diverse 5-Hetero-Functionalized Triazoles

4. Copper(I)-Catalyzed Interrupted Click Reaction: Synthesis of Diverse 5-Hetero-Functionalized Triazoles

5. A Reaction of Triazoles with Thioesters to Produce β‐Sulfanyl Enamides by Insertion of an Enamine Moiety into the Sulfur–Carbonyl Bond

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4. Diverse 3-Methylthio-4-Substituted Maleimides through a Novel Rearrangement Reaction: Synthesis and Selective Cell Imaging;The Journal of Organic Chemistry;2022-02-02

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