Iron‐Catalyzed Silylation and Spirocyclization of Biaryl‐Ynones: A Radical Cascade Process toward Silylated Spiro[5.5]trienones-Reference-Cited by-同舟云学术

Iron‐Catalyzed Silylation and Spirocyclization of Biaryl‐Ynones: A Radical Cascade Process toward Silylated Spiro[5.5]trienones

Published:2022-03-22 Issue:9 Volume:364 Page:1537-1542
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv Synth Catal

Author:

Chen Fei¹^ORCID,Zheng Yang¹,Yang Hao¹,Yang Qing‐Yun¹,Wu Lu‐Yan¹,Zhou Nengneng²^ORCID

Affiliation:

1. Henan Provincial Engineering and Technology Research Center for Precise Synthesis of Fluorine-Containing Drugs Anyang Key Laboratory of New Functional Complex Materials College of Chemistry and Chemical Engineering Anyang Normal University Anyang 455000 People's Republic of China

2. Key Laboratory of Functionalized Molecular Solids, Ministry of Education Anhui Key Laboratory of Molecule-Based Materials College of Chemistry and Materials Science Anhui Normal University Wuhu 241000 People's Republic of China

Funder

National Natural Science Foundation of China

Foundation of Henan Educational Committee

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200049

Reference124 articles.

2. Construction of spiro[5.5]undecanes containing a quaternary carbon atom adjacent to a spirocentre via an Ireland ester Claisen rearrangement and RCM reaction sequence. Total syntheses of (±)-α-chamigrene, (±)-β-chamigrene and (±)-laurencenone C

3. Cinnamylphenols from Phyllodium pulchellum

5. ICl-Induced Intramolecular Electrophilic Cyclization of 1-[4′-Methoxy(1,1′-biphenyl)2-yl]alkynones-A Facile Approach to Spiroconjugated Molecules

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