Nucleophilic addition of sulfoxonium ylides to hypervalent iodine diazo compounds as N-terminal electrophiles: direct access to novel functionalized hydrazones

The nucleophilic addition of sulfoxonium ylides to hypervalent Iodine diazo reagents as N-terminal electrophiles leads to highly functionalized hydrazones. The operational simplicity, wide scope, high product yields and mild conditions are notable features of the methodology.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00885a
Citations
1
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.94
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article

Nucleophilic addition of sulfoxonium ylides to hypervalent iodine diazo compounds as N-terminal electrophiles: direct access to novel functionalized hydrazones

Ruchir Kant, Namrata Rastogi, Varun Anand
1 citations
Organic Chemistry Frontiers
Cyclopropane Reaction Mechanisms
0.94
article

Nucleophilic addition of sulfoxonium ylides to hypervalent iodine diazo compounds as N-terminal electrophiles: direct access to novel functionalized hydrazones

Ruchir Kant, Namrata Rastogi, Varun Anand
article en
1 citations

Abstract

The nucleophilic addition of sulfoxonium ylides to hypervalent Iodine diazo reagents as N-terminal electrophiles leads to highly functionalized hydrazones. The operational simplicity, wide scope, high product yields and mild conditions are notable features of the methodology.

Organic Chemistry FrontiersVol. 12(24)
Central Drug Research Institute (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 22%
Cyclopropane Reaction Mechanisms
0.94
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