Iron(III) Triflate‐Assisted Skeletal Rearrangement of Warfarin Framework: A Direct Synthetic Route to a Diverse Series of Biorelevant Flavone‐Coumarin Molecular Hybrids

Abstract We herein disclose a new synthetic strategy for a diverse series of biologically interesting flavone‐coumarin molecular hybrids based on iron(III) triflate‐assisted direct and straightforward skeletal rearrangement of warfarin framework upon heating warfarin analogs in N , N‐ dimethylformamide (DMF). Good yields, reasonable reaction time, broad substrate scope and tolerance of various functional groups, scalability, and operational simplicity are the key features of this newly developed method.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2024-11-25
DOI
https://doi.org/10.1002/ajoc.202400676
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.25
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article

Iron(III) Triflate‐Assisted Skeletal Rearrangement of Warfarin Framework: A Direct Synthetic Route to a Diverse Series of Biorelevant Flavone‐Coumarin Molecular Hybrids

Anindita Bhowmick, Goutam Brahmachari
1 citations
Asian Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
0.25
article

Iron(III) Triflate‐Assisted Skeletal Rearrangement of Warfarin Framework: A Direct Synthetic Route to a Diverse Series of Biorelevant Flavone‐Coumarin Molecular Hybrids

Anindita Bhowmick, Goutam Brahmachari
article en
1 citations

Abstract

Abstract We herein disclose a new synthetic strategy for a diverse series of biologically interesting flavone‐coumarin molecular hybrids based on iron(III) triflate‐assisted direct and straightforward skeletal rearrangement of warfarin framework upon heating warfarin analogs in N , N‐ dimethylformamide (DMF). Good yields, reasonable reaction time, broad substrate scope and tolerance of various functional groups, scalability, and operational simplicity are the key features of this newly developed method.

Asian Journal of Organic ChemistryVol. 14(2)
Visva-Bharati University (IN)
Openalex Percentile: Top 46%
Oxidative Organic Chemistry Reactions
0.25
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