Ketocalixarenes: Versatile yet still Unexplored Macrocycles

Ori Shalev, Silvio E. Biali*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)216-225
Number of pages10
JournalSynlett
Volume36
Issue number3
DOIs
StatePublished - 12 Aug 2024

Bibliographical note

Publisher Copyright:
© 2024. The Author(s).

Keywords

  • calixarenes
  • cyclophanes
  • macrocycles
  • nucleophilic substitution
  • stereochemistry

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