The photoredox-catalyzed Meerwein addition reaction: intermolecular amino-arylation of alkenes

Durga Prasad Hari, Thea Hering, Burkhard König

Research output: Contribution to journalArticle (Academic Journal)peer-review

10 Downloads (Pure)

Abstract

A variety of amides are efficiently accessible under mild conditions by intermolecular amino-arylation using a photo Meerwein addition with visible light. The reaction has a broad substrate scope, tolerates a large range of functional groups, and was applied to the synthesis of a 3-aryl-3,4-dihydroisoquinoline.

Original languageEnglish
Pages (from-to)725-728
Number of pages4
JournalAngewandte Chemie - International Edition
Volume53
Issue number3
Early online date4 Dec 2013
DOIs
Publication statusPublished - 13 Jan 2014

Bibliographical note

Acceptance date is provisional and based on date of publication.

Keywords

  • amino-arylation
  • aryl radicals
  • Meerwein addition
  • photocatalysis
  • visible light

Fingerprint Dive into the research topics of 'The photoredox-catalyzed Meerwein addition reaction: intermolecular amino-arylation of alkenes'. Together they form a unique fingerprint.

Cite this