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Cascade N-Alkylation/Hemiacetalization for Facile Construction of the Spiroketal Skeleton of Acortatarin Alkaloids with Therapeutic Potentiality in Diabetic Nephropathy |
Pei Cao1, Zhen-Jie Li1, Wen-Wu Sun1,2, Shashwat Malhotra3,4, Yuan-Liang Ma1, Bin Wu1, Virinder S. Parmar3 |
1. State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, People's Republic of China; 2. University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China; 3. Bioorganic Laboratory, Department of Chemistry, University of Delhi, Delhi 110007, India; 4. Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustrasse 3, 14195 Berlin, Germany |
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Abstract The concise building of the spiroketal core of acortatarin-type alkaloids as potential therapeutic agents in diabetic nephropathy was established in four steps, through a tandem N-alkylation/hemiacetalization between pyrrole units and the corresponding halo alcohols generated by convenient halomethylation of chiral lactones from natural aldoses.
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Keywords
Acortatarin alkaloids
Diabetic nephropathy
N-alkylation/hemiacetalization
Halomethylation
Chiral lactones
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Fund:This research was supported by grants from the "Hundred Talents Project" of Chinese Academy of Science and "High-end Science and Technology Talents Program" of Yunnan Province(2011HA008). |
Issue Date: 11 February 2018
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