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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Redox-Annulations of Cyclic Amines with 2-(2-Oxoethyl)malonates
Zhengbo Zhu1,2, Hemant S Chandak2, Daniel Seidel1,2
1Center for Heterocyclic Compounds, Department of Chemistry , University of Florida , Gainesville , Florida 32611 , United States.
Abstract:
Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-(2-oxoethyl)malonates in the presence of catalytic amounts of benzoic acid. These reactions install a fully saturated five-membered ring and provide access to structures closely related to the natural products crispine A and harmicine.
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