Synthesis of Fused Isoxazoles via Intramolecular Nitrile Oxide Cycloaddition

Abstract We report an efficient and straightforward strategy for the synthesis of substituted dihydrofuro[3,4‐c]isoxazoles and dihydro‐4H‐pyrano[4,3‐c]isoxazoles via intramolecular nitrile oxide cycloaddition (INOC) reactions of aldoximes, employing (diacetoxyiodo)benzene (PIDA/DIB/PhI(OAc)₂) as a single, cost‐effective oxidizing agent. This method enables the practical and economical synthesis of structurally diverse and highly functionalized oxygen‐bridged isoxazole derivatives under mild reaction condition with short reaction time.

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Journal
ChemistrySelect
Published
2025-04-29
DOI
https://doi.org/10.1002/slct.202501315
Citations
2
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Synthesis of Fused Isoxazoles via Intramolecular Nitrile Oxide Cycloaddition

Rohit Maurya, Mahender Khatravath, Ashutosh Dey, Megha Kumari et al.
2 citations
ChemistrySelect
Synthesis and Catalytic Reactions
1.87
article

Synthesis of Fused Isoxazoles via Intramolecular Nitrile Oxide Cycloaddition

Rohit Maurya, Mahender Khatravath, Ashutosh Dey, Megha Kumari, Vikash Kumar
article en
2 citations

Abstract

Abstract We report an efficient and straightforward strategy for the synthesis of substituted dihydrofuro[3,4‐c]isoxazoles and dihydro‐4H‐pyrano[4,3‐c]isoxazoles via intramolecular nitrile oxide cycloaddition (INOC) reactions of aldoximes, employing (diacetoxyiodo)benzene (PIDA/DIB/PhI(OAc)₂) as a single, cost‐effective oxidizing agent. This method enables the practical and economical synthesis of structurally diverse and highly functionalized oxygen‐bridged isoxazole derivatives under mild reaction condition with short reaction time.

ChemistrySelectVol. 10(17)
Central University of South Bihar (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Science and Engineering Research Board
Openalex Percentile: Top 16%
Synthesis and Catalytic Reactions
1.87
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