<div><p>Two macrocyclic compounds containing propargylamine backbone have been synthesised via Mannich three-component reaction. The macrocycle <b>3a</b> shows the intramolecular self-folding conformation. The macrocycle <b>3b</b> self-assembles via multiple weak interactions to form a multiple double-helical system, which shows the alternate helical handedness.</p></div
N-Substituted aromatic cyclooligoamides composed of different combinations of ortho-, meta-, and/or ...
The self-assembling abilities of several pseudopeptidic macrocycles have been thoroughly studied bot...
Oligoamide macrocycles with a backbone partially constrained by hydrogen bonds have been prepared. T...
Naphthyridine-based macrocycles with urea and formamidine linkages and pyridazine-based macrocyclic ...
In the absence of preorganization, macrocyclization reactions are often plagued by oligomeric and po...
The formation of well-defined, discrete self-assembled architectures relies on the interplay between...
New 18-membered hexaaza (3 and 4) and 24-membered octaaza (7 and 8) macrocycles with 2-hydroxy-3,5-d...
With the long term aim of preparing synthetic macromolecules that mimic the folding actions of natur...
The alkylation of some secondary amide functions with a dimethoxybenzyl (DMB) group in oligomers of ...
Transannular hydrogen bonding stabilizes a left-handed double helical conformation in the tryptophan...
Enantiomorphic right- and left-handed polyproline type I helices in four cyclic dodecapeptoids with ...
The alkylation of some secondary amide functions with a dimethoxybenzyl (DMB) group in oligomers of ...
Abstract. The design and synthesis of figure–eight macrocycles are very scarce owing to the intricac...
A new synthetic strategy for macrocycles bearing multiple coordination moieties was developed. A sel...
10.1007/s10847-012-0243-4Journal of Inclusion Phenomena and Macrocyclic Chemistry761-21-11JIPC
N-Substituted aromatic cyclooligoamides composed of different combinations of ortho-, meta-, and/or ...
The self-assembling abilities of several pseudopeptidic macrocycles have been thoroughly studied bot...
Oligoamide macrocycles with a backbone partially constrained by hydrogen bonds have been prepared. T...
Naphthyridine-based macrocycles with urea and formamidine linkages and pyridazine-based macrocyclic ...
In the absence of preorganization, macrocyclization reactions are often plagued by oligomeric and po...
The formation of well-defined, discrete self-assembled architectures relies on the interplay between...
New 18-membered hexaaza (3 and 4) and 24-membered octaaza (7 and 8) macrocycles with 2-hydroxy-3,5-d...
With the long term aim of preparing synthetic macromolecules that mimic the folding actions of natur...
The alkylation of some secondary amide functions with a dimethoxybenzyl (DMB) group in oligomers of ...
Transannular hydrogen bonding stabilizes a left-handed double helical conformation in the tryptophan...
Enantiomorphic right- and left-handed polyproline type I helices in four cyclic dodecapeptoids with ...
The alkylation of some secondary amide functions with a dimethoxybenzyl (DMB) group in oligomers of ...
Abstract. The design and synthesis of figure–eight macrocycles are very scarce owing to the intricac...
A new synthetic strategy for macrocycles bearing multiple coordination moieties was developed. A sel...
10.1007/s10847-012-0243-4Journal of Inclusion Phenomena and Macrocyclic Chemistry761-21-11JIPC
N-Substituted aromatic cyclooligoamides composed of different combinations of ortho-, meta-, and/or ...
The self-assembling abilities of several pseudopeptidic macrocycles have been thoroughly studied bot...
Oligoamide macrocycles with a backbone partially constrained by hydrogen bonds have been prepared. T...