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Rhodium(III)-Catalyzed Redox-Neutral [3+3] Annulation of N-nitrosoanilines with Cyclopropenones: A Traceless Approach to Quinolin-4(1H)-One Scaffolds.


ABSTRACT: A traceless approach to quinolin-4(1H)-one scaffolds through Rh(III)-catalyzed redox-neutral [3+3] cyclization of N-nitrosoanilines with cyclopropenones has been achieved. This protocol features short reaction time and atom-economical combination without extra additives, which can be further applied in the construction of privileged heterocyclic compounds in pharmaceutical chemistry.

SUBMITTER: Liu L 

PROVIDER: S-EPMC7024356 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Rhodium(III)-Catalyzed Redox-Neutral [3+3] Annulation of <i>N</i>-nitrosoanilines with Cyclopropenones: A Traceless Approach to Quinolin-4(1<i>H</i>)-One Scaffolds.

Liu Lingjun L   Li Jiyuan J   Dai Wenhao W   Gao Feng F   Chen Kaixian K   Zhou Yu Y   Liu Hong H  

Molecules (Basel, Switzerland) 20200109 2


A traceless approach to quinolin-4(1<i>H</i>)-one scaffolds through Rh(III)-catalyzed redox-neutral [3+3] cyclization of <i>N</i>-nitrosoanilines with cyclopropenones has been achieved. This protocol features short reaction time and atom-economical combination without extra additives, which can be further applied in the construction of privileged heterocyclic compounds in pharmaceutical chemistry. ...[more]

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