Preparation of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams <i>via</i> a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation

An efficient synthesis of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams has been developed through a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation of functionalized nitriles and 2-arylketones for the first time.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob01300c
Primary Topic
Chemical Synthesis and Reactions
Type
article
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article

Preparation of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams via a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation

Yue‐Hong Hu, Zhang‐Yan Gan, Chengcheng Yu, Xiao‐Ming Zhang et al.
Organic & Biomolecular Chemistry
Chemical Synthesis and Reactions
article

Preparation of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams via a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation

Yue‐Hong Hu, Zhang‐Yan Gan, Chengcheng Yu, Xiao‐Ming Zhang, Fu‐Min Zhang, Meng-En Chen, Yuting Chen, J. Mo
article en

Abstract

An efficient synthesis of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams has been developed through a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation of functionalized nitriles and 2-arylketones for the first time.

Organic & Biomolecular ChemistryVol. 23(42)
Lanzhou University (CN)
Openalex Percentile: Top 80%
Chemical Synthesis and Reactions
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Preparation of α,β,γ,γ-tetrasubstituted α,β-unsaturated γ-lactams <i>via</i> a tandem or one-pot oxidative Ritter reaction/Knoevenagel condensation — Yue‐Hong Hu, Zhang‐Yan Gan, et al. · Organic & Biomolecular Chemistry (2025) | TGRS Research Map | TGRS