Stable sulfonate esters as C1-synthons for cyclopropanation reaction to access antimicrobial active 3,3′-spirocyclopropyloxindoles

A NaH-mediated formal [2 + 1] annulation using stable while reactive 4-nitrophenyl sulfonates as C1 synthons for the efficient synthesis of spirocyclopropyloxindoles with promising antibacterial activity against plant pathogens was disclosed.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00153f
Citations
1
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.94
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article

Stable sulfonate esters as C1-synthons for cyclopropanation reaction to access antimicrobial active 3,3′-spirocyclopropyloxindoles

Yijie Long, Xingxing Wu, Hongyan Long, Yi‐Wen Huang et al.
1 citations
Organic Chemistry Frontiers
Cyclopropane Reaction Mechanisms
0.94
article

Stable sulfonate esters as C1-synthons for cyclopropanation reaction to access antimicrobial active 3,3′-spirocyclopropyloxindoles

Yijie Long, Xingxing Wu, Hongyan Long, Yi‐Wen Huang, Pan Feng
article en
1 citations

Abstract

A NaH-mediated formal [2 + 1] annulation using stable while reactive 4-nitrophenyl sulfonates as C1 synthons for the efficient synthesis of spirocyclopropyloxindoles with promising antibacterial activity against plant pathogens was disclosed.

Organic Chemistry FrontiersVol. 12(13)
Guizhou University (CN)
Openalex Percentile: Top 28%
Cyclopropane Reaction Mechanisms
0.94
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