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Photoredox-catalyzed multicomponent Petasis reaction in batch and continuous flow with alkyl boronic acids.


ABSTRACT: Multicomponent reactions (MCRs) are ideal platforms for the generation of a wide variety of organic scaffolds in a convergent and atom-economical manner. Many strategies for the generation of highly substituted and diverse structures have been developed and among these, the Petasis reaction represents a viable reaction manifold for the synthesis of substituted amines via coupling of an amine, an aldehyde and a boronic acid (BA). Despite its synthetic utility, the inherent drawbacks associated with the traditional two-electron Petasis reaction have stimulated continuous research towards more facile and tolerant methodologies. In this regard, we present the use of free alkyl BAs as effective radical precursors in this MCR through a single-electron transfer mechanism under mild reaction conditions. We have further demonstrated its applicability to photo-flow reactors, facilitating the reaction scale-up for the rapid assembly of complex molecular structures.

SUBMITTER: Oliva M 

PROVIDER: S-EPMC8487034 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Photoredox-catalyzed multicomponent Petasis reaction in batch and continuous flow with alkyl boronic acids.

Oliva Monica M   Ranjan Prabhat P   Pillitteri Serena S   Coppola Guglielmo Attilio GA   Messina Monica M   Van der Eycken Erik V EV   Sharma Upendra Kumar UK  

iScience 20210915 10


Multicomponent reactions (MCRs) are ideal platforms for the generation of a wide variety of organic scaffolds in a convergent and atom-economical manner. Many strategies for the generation of highly substituted and diverse structures have been developed and among these, the Petasis reaction represents a viable reaction manifold for the synthesis of substituted amines <i>via</i> coupling of an amine, an aldehyde and a boronic acid (BA). Despite its synthetic utility, the inherent drawbacks associ  ...[more]

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