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Facile Synthesis of 2H-Benzo[h]Chromenes via an Arylamine-Catalyzed Mannich Cyclization Cascade Reaction.


ABSTRACT: A simple arylamine-catalyzed Mannich-cyclization cascade reaction was developed for facile synthesis of substituted 2H-benzo[h]chromenes. The notable feature of the process included the efficient generation of ortho-quinone methides (o-QMs) catalyzed by a simple aniline. The mild reaction conditions allowed for a broad spectrum of 1- and 2-naphthols and trans-cinnamaldehydes to engage in the cascade sequence with high efficiency.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC8231631 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Facile Synthesis of 2<i>H</i>-Benzo[<i>h</i>]Chromenes via an Arylamine-Catalyzed Mannich Cyclization Cascade Reaction.

Zhang Yueteng Y   Ji Peng P   Meng Xiang X   Gao Feng F   Zeng Fanxun F   Wang Wei W  

Molecules (Basel, Switzerland) 20210612 12


A simple arylamine-catalyzed Mannich-cyclization cascade reaction was developed for facile synthesis of substituted 2<i>H</i>-benzo[<i>h</i>]chromenes. The notable feature of the process included the efficient generation of <i>ortho</i>-quinone methides (<i>o</i>-QMs) catalyzed by a simple aniline. The mild reaction conditions allowed for a broad spectrum of 1- and 2-naphthols and <i>trans</i>-cinnamaldehydes to engage in the cascade sequence with high efficiency. ...[more]

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