BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers
- 1 January 2011
- journal article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 47 (46) , 12488-12490
Abstract
We report here, for the first time, the BOP-mediated one-pot macrocyclization that is facilitated and guided by internally placed intramolecular H-bonds to allow for the highly selective formation of five-residue cation-binding macrocycles.Keywords
This publication has 38 references indexed in Scilit:
- Efficient Kinetic MacrocyclizationJournal of the American Chemical Society, 2009
- A Proline-based Macrocyclic Amide with S4 SymmetryChemistry Letters, 2007
- Shape‐Persistent Aromatic Amide Oligomers: New Tools for Supramolecular ChemistryChemistry – An Asian Journal, 2006
- [6 + 6] Schiff-base macrocycles with 12 imines: giant analogues of cyclohexaneChemical Communications, 2006
- Aromatic Oligoureas: Enforced Folding and Assisted CyclizationOrganic Letters, 2006
- Hydrogen bond directed synthesis of pyridazine and naphthyridine containing macrocyclesChemical Communications, 2005
- Highly Efficient, One-Step Macrocyclizations Assisted by the Folding and Preorganization of Precursor OligomersJournal of the American Chemical Society, 2004
- Strained Aromatic Oligoamide Macrocycles as New Molecular ClipsOrganic Letters, 2004
- Evolution of Helical FoldamersCurrent Organic Chemistry, 2003
- Directed macrocyclisation reactionsJournal of the Chemical Society, Chemical Communications, 1994