Abstract
A bis-ferrocene macrocycle was synthesized by reversible acylhydrazone formation under thermodynamic control, starting from a ferrocene functionalized with hydrazide and protected aldehyde moieties. A hydrogen sulfate anion acts as a template to direct the synthesis specifically toward the macrocyclic dimer, due to a weak but selective binding interaction. This work highlights the utility of dynamic combinatorial chemistry as an approach to macrocycle synthesis.
| Original language | English |
|---|---|
| Article number | ST-2023-09-0406-L |
| Journal | Synlett |
| Volume | 34 |
| Pages (from-to) | A-F |
| ISSN | 0936-5214 |
| DOIs | |
| Publication status | Published - 2023 |
Keywords
- Dynamic combinatorial chemistry
- Ferrocene
- Host-guest systems
- Hydrazones
- Macrocycles
- Supramolecular chemistry
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