Synthesis of 6,16,22,32-tetrahydroxy[3.3.3.3]metacyclophane with the aid of a new copper catalyst
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Complexation of Neutral Molecules by Cyclophane Hosts
2. Synthesis and characterization of [3.3.3.3]metacyclophane
3. Molecular recognition in water: new receptors for adenine derivatives
4. Molecular recognition in aqueous media. New binding studies provide further insights into the cation-.pi. interaction and related phenomena
Cited by 4 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. Formation of Alkanes and Arenes by Coupling Reactions;Comprehensive Organic Transformations;2018-02-28
2. ChemInform Abstract: Synthesis of 6,16,22,32-Tetrahydroxy(3.3.3.3)metacyclophane with the Aid of a New Copper Catalyst.;ChemInform;2010-08-18
3. Synthesis, Modification, and Characterization of a Family of Homologues of exo-Calix[4]arene: exo-[n.m.n.m]Metacyclophanes, n,m ≥ 3;The Journal of Organic Chemistry;2000-08-01
4. Scope and Utility of a New Soluble Copper Catalyst [CuBr−LiSPh−LiBr−THF]: A Comparison with Other Copper Catalysts in Their Ability to Couple One Equivalent of a Grignard Reagent with an Alkyl Sulfonate;Journal of the American Chemical Society;1997-03-01
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