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![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Synthesis of C(CF3)Me2 Tetrahydropyridazines and Dihydropyrazoles via Radical Cascade and Mechanistic Studies by DFT
Shijie Zhang1, Yujie Huang1, Lu'er Jin2
1Zhejiang Key Laboratory of Advanced Chemical Engineering Manufacture Technology, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou310058, P. R. China.
Abstract:
Herein, we report a metal-free radical cascade cyclization initiated by 1,1-dimethyl-2,2,2-trifluoroethyl radicals. Readily available trifluoromethyl-substituted carboxylic acids were used as radical precursors and reacted with N-homoallyl or N-allyl aldehyde hydrazones to afford 1,1-dimethyl-2,2,2-trifluoroethylated tetrahydropyridazine and dihydropyrazole derivatives. Under the optimized conditions, 25 examples were obtained in moderate to good yields. The reaction proceeds without metal catalysts, highlighting its operational simplicity and practical utility in the synthesis of fluorinated nitrogen heterocycles. Density functional theory calculations were performed to elucidate the radical reaction mechanism.
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