tert-Butyl Nitrite-Induced Radical Nitrile Oxidation Cycloaddition: Synthesis of Isoxazole/Isoxazoline-Fused Benzo 6/7/8-membered Oxacyclic Ketones

Author:

Cao Jian-Kang1,Cao Tian-Zheng1,Yue Qian-Wen1,Ma Ying1,Yang Chuan-Ming1,Zhang Hong-Xi1,Li Ya-Chen1,Dong Qiao-Ke1,Zhu Yan-Ping12ORCID,Sun Yuan-Yuan1

Affiliation:

1. Key Laboratory of Molecular Pharmacology and Drug Evaluation, Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, School of Pharmacy, Yantai University, Yantai 264005, China

2. Anhui Laboratory of Molecule-Based Materials, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, China

Abstract

A practical metal-free and additive-free approach for the synthesis of 6/7/8-membered oxacyclic ketone-fused isoxazoles/isoxazolines tetracyclic or tricyclic structures is reported through Csp3–H bond radical nitrile oxidation and the intramolecular cycloaddition of alkenyl/alkynyl-substituted aryl methyl ketones. This convenient approach enables the simultaneous formation of isoxazole/isoxazoline and 6/7/8-membered oxacyclic ketones to form polycyclic architectures by using tert-butyl nitrite (TBN) as a non-metallic radical initiator and N–O fragment donor.

Funder

Yantai’s “Double Hundred Plan”

Talent Induction Program for Youth Innovation Teams in Colleges and Universities of Shandong Province

Foundation of Anhui Laboratory of Molecule-Based Materials

The Graduate Innovation Foundation of Yantai University

Publisher

MDPI AG

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