Transition-metal-free coupling reactions
CL Sun, ZJ Shi - Chemical reviews, 2014 - ACS Publications
Transition-metal-catalyzed reactions have been studied since the very beginning of the past
century and represent a great success in organic chemistry, along with the birth and growth …
century and represent a great success in organic chemistry, along with the birth and growth …
[HTML][HTML] Macrocyclization reactions: the importance of conformational, configurational, and template-induced preorganization
V Marti-Centelles, MD Pandey, MI Burguete… - Chemical …, 2015 - ACS Publications
Macrocyclic structures are common synthetic targets in drug discovery,(1, 2) and therefore,
interest in their study is continuously increasing in this field.(3, 4) A classic example is …
interest in their study is continuously increasing in this field.(3, 4) A classic example is …
Aromatic amide foldamers: structures, properties, and functions
DW Zhang, X Zhao, JL Hou, ZT Li - Chemical reviews, 2012 - ACS Publications
The past several decades have witnessed great progress in the understanding of the high-
order structure of biomacromolecules. Currently, it is well-recognized that folding of proteins …
order structure of biomacromolecules. Currently, it is well-recognized that folding of proteins …
[HTML][HTML] A pentagonal cyanostar macrocycle with cyanostilbene CH donors binds anions and forms dialkylphosphate [3] rotaxanes
S Lee, CH Chen, AH Flood - Nature chemistry, 2013 - nature.com
Since the discovery of crown ethers, macrocycles have been recognized as powerful
platforms for supramolecular chemistry. Although their numbers and variations are now …
platforms for supramolecular chemistry. Although their numbers and variations are now …
Self-assembled macrocycles: design strategies and emerging functions
D Talukdar, JM Kumar, B Gole - Crystal Growth & Design, 2023 - ACS Publications
Molecular self-assembly is an essential process in biological systems to perform
sophisticated functions. Along the same line, development of artificial self-assembled …
sophisticated functions. Along the same line, development of artificial self-assembled …
Pyridine/Oxadiazole‐Based Helical Foldamer Ion Channels with Exceptionally High K+/Na+ Selectivity
Protein channels are characterized by high transport selectivity, which is essential for
maintaining cellular function. Efforts to reproduce such high selectivity over the past four …
maintaining cellular function. Efforts to reproduce such high selectivity over the past four …
Hybrid Pyridine–Pyridone Foldamer Channels as M2‐Like Artificial Proton Channels
Currently, completely abiotic channel systems that concurrently reproduce the high
selectivity and high permeation rate of natural protein channels are rare. Here, we provide …
selectivity and high permeation rate of natural protein channels are rare. Here, we provide …
Proton gradient-induced water transport mediated by water wires inside narrow aquapores of aquafoldamer molecules
H Zhao, S Sheng, Y Hong, H Zeng - Journal of the American …, 2014 - ACS Publications
Hollow tubular aquapores inside aquafoldamers can be created via the “sticky” end-
mediated formation of 1D chiral helical stacks involving same-handed helices, and are …
mediated formation of 1D chiral helical stacks involving same-handed helices, and are …
Cavity-containing aromatic oligoamide foldamers and macrocycles: progress and future perspectives
As a major class of foldamers, aromatic oligoamide foldamers have attracted intense
interest. The rigidity of aromatic residues and amide linkages allows the development of …
interest. The rigidity of aromatic residues and amide linkages allows the development of …
A macrocyclic aromatic pyridone pentamer as a highly efficient organocatalyst for the direct arylations of unactivated arenes
H Zhao, J Shen, J Guo, R Ye, H Zeng - Chemical Communications, 2013 - pubs.rsc.org
A macrocyclic aromatic pyridone pentamer as a highly efficient organocatalyst for the direct
arylations of unactivated arenes - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC00019B …
arylations of unactivated arenes - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC00019B …