AgNO<sub>3</sub>‐Catalyzed Regio‐selective Bis‐heteroannulation of <i>o</i>‐Hydroxyphenyl Enaminones and Yne‐enones: A Facile synthesis of Functionalized 3‐(Furan‐3‐ylmethyl) Chromones

Abstract An efficient AgNO 3 ‐catalyzed regio‐selective bis‐heteroannulation of o ‐hydroxyphenyl enaminones with yne‐enones for the synthesis of highly functionalized 3‐(furan‐3‐ylmethyl) chromones has been developed. The protocol enables the simultaneous construction of chromone and furan skeleton in one‐step cascade reaction. Furthermore, high easily accessible starting materials, regioselectivity, room temperature, good to excellent yields, broad substituent tolerance, further gram‐scale synthesis and derivatization make this strategy potential synthetic application value in synthetic and medicinal chemistry.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-11
DOI
https://doi.org/10.1002/adsc.202500172
Citations
4
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
3.74
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article

AgNO3‐Catalyzed Regio‐selective Bis‐heteroannulation of o‐Hydroxyphenyl Enaminones and Yne‐enones: A Facile synthesis of Functionalized 3‐(Furan‐3‐ylmethyl) Chromones

Mingshuai Zhang, Zhilai Zhang, Fuchao Yu, Ying Xu et al.
4 citations
Advanced Synthesis & Catalysis
Catalytic Alkyne Reactions
3.74
article

AgNO3‐Catalyzed Regio‐selective Bis‐heteroannulation of o‐Hydroxyphenyl Enaminones and Yne‐enones: A Facile synthesis of Functionalized 3‐(Furan‐3‐ylmethyl) Chromones

Mingshuai Zhang, Zhilai Zhang, Fuchao Yu, Ying Xu, Xiaohong Wang, Yongchao Wang, Meichen Liu, Yijin Wang, Menglin Peng
article en
4 citations

Abstract

Abstract An efficient AgNO 3 ‐catalyzed regio‐selective bis‐heteroannulation of o ‐hydroxyphenyl enaminones with yne‐enones for the synthesis of highly functionalized 3‐(furan‐3‐ylmethyl) chromones has been developed. The protocol enables the simultaneous construction of chromone and furan skeleton in one‐step cascade reaction. Furthermore, high easily accessible starting materials, regioselectivity, room temperature, good to excellent yields, broad substituent tolerance, further gram‐scale synthesis and derivatization make this strategy potential synthetic application value in synthetic and medicinal chemistry.

Advanced Synthesis & CatalysisVol. 367(10)
Kunming University of Science and Technology (CN), Yunnan Normal University (CN)
Openalex Percentile: Top 8%
Catalytic Alkyne Reactions
3.74
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