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.
Authors
- Mingshuai Zhang
- Zhilai Zhang (ORCID: https://orcid.org/0009-0007-4070-3674)
- Fuchao Yu (ORCID: https://orcid.org/0000-0001-5557-3824)
- Ying Xu (ORCID: https://orcid.org/0000-0001-9994-9889)
- Xiaohong Wang (ORCID: https://orcid.org/0009-0006-0732-9871)
- Yongchao Wang (ORCID: https://orcid.org/0000-0003-2248-6630)
- Meichen Liu (ORCID: https://orcid.org/0000-0003-4536-5444)
- Yijin Wang (ORCID: https://orcid.org/0000-0001-5488-3089)
- Menglin Peng
Institutions
- Kunming University of Science and Technology (CN)
- Yunnan Normal University (CN)
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