Abstract
Ketocalix[ n ]arenes can be prepared via oxidation of the methylene groups of protected calix[ n ]arenes. The presence of carbonyl groups at the bridges alters the preferred conformation and reactivity of the macrocycle and provides an entry point (via nucleophilic additions reactions) to a wide array of methylene-substituted derivatives as well as calix[ n ]radialenes. 1 Introduction 2 Synthesis of Ketocalix[ n ]arenes 2.1 Ketocalix[4]arene Derivatives 2.2 Systems Possessing both Carbonyl and Bromomethane Bridges 2.3 Pentaoxoketocalix[5]arene and Hexaoxoketocalix[6]arene Derivatives 2.4 Monooxo- and Dioxoketocalix[6]arenes 3 Conformation of Ketocalixarenes 4 Reactions of Ketocalixarenes 4.1 Alkylation of the OH Groups 4.2 Intramolecular Aromatic Nucleophilic Substitution 4.3 Reduction of the Carbonyl Groups 4.4 Reaction of 5c with PhLi 4.5
Original language | English |
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Pages (from-to) | 216-225 |
Number of pages | 10 |
Journal | Synlett |
Volume | 36 |
Issue number | 3 |
DOIs | |
State | Published - 12 Aug 2024 |
Bibliographical note
Publisher Copyright:© 2024. The Author(s).
Keywords
- calixarenes
- cyclophanes
- macrocycles
- nucleophilic substitution
- stereochemistry