Synthesis of the Spermidine Alkaloids (−)-(2R,3R)- and (−)-(2R,3S)-3-Hydroxycelacinnine: Macrocyclization with Oxirane-Ring Opening and Inversion via Cyclic Sulfamidates
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The untapped potential of spermidine alkaloids: Sources, structures, bioactivities and syntheses;European Journal of Medicinal Chemistry;2022-10
2. Stereoselective synthesis of cis-2,6-disubstituted piperidines from 1,2-cyclic sulfamidates;Tetrahedron;2019-03
3. Natural Occurrence, Synthesis and Biological Applications of Spermidine Alkaloids;Current Organic Chemistry;2017-01-27
4. Diastereoselective Synthesis and Configurational Assignment of Novel Functionalized Cyclic Sulfamidites Precursors of Cyclic Sulfamidates;Heteroatom Chemistry;2016-02-12
5. Concise Preparation of a Stable Cyclic Sulfamidate Intermediate in the Synthesis of a Enantiopure Chiral Active Diamine Derivative;Organic Process Research & Development;2015-03-31
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