Eosin‐Y‐Catalyzed Photoredox C−S Bond Formation: Easy Access to Thioethers

An operationally simple Eosin Y catalyzed sulfenylation of hydrazones has been realized to afford a range of thioethers under visible light. The methodology provides high yields of thioethers under ambient conditions employing readily available and inexpensive starting materials. The reaction has br...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry, an Asian journal an Asian journal, 2019-12, Vol.14 (24), p.4712-4716
Main Authors: Chand, Shiv, Pandey, Anand Kumar, Singh, Rahul, Kumar, Saurabh, Singh, Krishna Nand
Format: Article
Language:English
Subjects:
Chemistry
Eosin Y
Functional groups
Hydrazones
photoredox catalysis
Substrates
sulfenylation
thioethers
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:An operationally simple Eosin Y catalyzed sulfenylation of hydrazones has been realized to afford a range of thioethers under visible light. The methodology provides high yields of thioethers under ambient conditions employing readily available and inexpensive starting materials. The reaction has broad substrate scope and is compatible with various functional groups. Photoredox sulfenylation: An operationally simple and efficient photoredox strategy has been realised for the C−S bond formation, employing organic dye Eosin Y as catalyst. The methodology offers a broad substrate scope and functional group tolerance.
ISSN:1861-4728
1861-471X
DOI:10.1002/asia.201901060