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A New, Convenient Way to Fully Substituted α,β-Unsaturated γ-Hydroxy Butyrolactams.


ABSTRACT: The synthesis of novel, highly functionalized 5-hydroxy 3-pyrrolin-2-ones via a two-step procedure involving an addition reaction between KCN and corresponding chalcones, followed by ring condensation of the obtained β-cyano ketones with het(aryl)aldehydes under basic conditions is described. This protocol enables the preparation of various 3,5-di-aryl/heteroaryl-4-benzyl substituted α,β-unsaturated γ-hydroxy butyrolactams, which are subjects of significant interest to synthetic organic and medicinal chemistry.

SUBMITTER: Aksenov AV 

PROVIDER: S-EPMC10299564 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature

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A New, Convenient Way to Fully Substituted α,β-Unsaturated γ-Hydroxy Butyrolactams.

Aksenov Alexander V AV   Aksenov Dmitrii A DA   Kurenkov Igor A IA   Leontiev Alexander V AV   Aksenov Nicolai A NA  

International journal of molecular sciences 20230616 12


The synthesis of novel, highly functionalized 5-hydroxy 3-pyrrolin-2-ones via a two-step procedure involving an addition reaction between KCN and corresponding chalcones, followed by ring condensation of the obtained β-cyano ketones with het(aryl)aldehydes under basic conditions is described. This protocol enables the preparation of various 3,5-di-aryl/heteroaryl-4-benzyl substituted α,β-unsaturated γ-hydroxy butyrolactams, which are subjects of significant interest to synthetic organic and medi  ...[more]

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