A two-step Kinugasa/Conia-ene-type sequential reaction for the asymmetric synthesis of 8-methylene-2,6-diazaspiro[3.4]octane-1,5-diones

A two-step Kinugasa/Conia-ene-type sequential reaction is developed. The process provided a simple and efficient access to chiral 8-methylene-2,6-diazaspiro[3.4]octane-1,5-diones.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-10-28
DOI
https://doi.org/10.1039/d4qo01388c
Citations
4
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.83
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article

A two-step Kinugasa/Conia-ene-type sequential reaction for the asymmetric synthesis of 8-methylene-2,6-diazaspiro[3.4]octane-1,5-diones

Shanyue Li, Haowen Ma, Wei Zhou, Bohua Wu et al.
4 citations
Organic Chemistry Frontiers
Fluorine in Organic Chemistry
0.83
article

A two-step Kinugasa/Conia-ene-type sequential reaction for the asymmetric synthesis of 8-methylene-2,6-diazaspiro[3.4]octane-1,5-diones

Shanyue Li, Haowen Ma, Wei Zhou, Bohua Wu, Qian Cai, Qicai Ma
article en
4 citations

Abstract

A two-step Kinugasa/Conia-ene-type sequential reaction is developed. The process provided a simple and efficient access to chiral 8-methylene-2,6-diazaspiro[3.4]octane-1,5-diones.

Organic Chemistry FrontiersVol. 12(1)
Zhejiang Normal University (CN), Jinan University (CN)
Openalex Percentile: Top 31%
Fluorine in Organic Chemistry
0.83
DOISourceOpenAlex
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