Shape-persistent H-bonded macrocyclic aromatic pentamers
Authors:
- 12 December 2012
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 49 (39) , 4127-4144
Abstract
The use of multiple-center intramolecular H-bonds for the efficient construction of macrocycles of varying structures and functions is among the newest and the most noteworthy additions to the toolbox for macrocycle synthesis. This strategy has allowed the creation of sizable interior cavities as small as 2.8 Å and as large as 15 Å in radius in these H-bonded macrocycles with a number of them expressing tailor-made functions. While concentrating on our recent contributions to this fast-growing field, we will further summarize the latest advances on the design, synthesis, structure and function of these shape-persistent H-bonded macrocyclic foldamers that have helped to create a whole new dimension of scientific research, markedly expanding both the structural and functional repertoires of shape-persistent macrocycles.Keywords
This publication has 85 references indexed in Scilit:
- Aromatic Amide Foldamers: Structures, Properties, and FunctionsChemical Reviews, 2012
- BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamersChemical Communications, 2011
- Macrocyclic and Helical Oligoamides as a New Class of G-Quadruplex LigandsJournal of the American Chemical Society, 2007
- Fit To Be Tied: Conformation-Directed Macrocyclization of Peptoid FoldamersOrganic Letters, 2007
- Macrocyclic scaffolds derived from p-aminobenzoic acidChemical Communications, 2007
- Shape-persistent macrocyclic aromatic tetrasulfonamides: Molecules with nanosized cavities and their nanotubular assemblies in solid stateProceedings of the National Academy of Sciences, 2006
- Phenanthroline Dicarboxamide-Based Helical Foldamers: Stable Helical Structures in MethanolThe Journal of Organic Chemistry, 2006
- Hydrogen bond directed synthesis of pyridazine and naphthyridine containing macrocyclesChemical Communications, 2005
- Aromatic δ-PeptidesJournal of the American Chemical Society, 2003
- CaCl3- or Ca2Cl4 Complexing Cyclic Aromatic Amide. Template Effect on CyclizationJournal of the American Chemical Society, 1996