The Photoredox‐Catalyzed Meerwein Addition Reaction: Intermolecular Amino‐Arylation of Alkenes | Zendy

Prasad Hari Durga | Zendy; Hering Thea | Zendy; König Burkhard | Zendy

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The Photoredox‐Catalyzed Meerwein Addition Reaction: Intermolecular Amino‐Arylation of Alkenes

Author(s) -

Prasad Hari Durga,

Hering Thea,

König Burkhard

Publication year - 2014

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201307051

Subject(s) - intermolecular force , photoredox catalysis , chemistry , catalysis , aryl , combinatorial chemistry , substrate (aquarium) , functional group , scope (computer science) , photochemistry , organic chemistry , molecule , photocatalysis , computer science , biology , polymer , alkyl , ecology , programming language

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.

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