Coordination chemistry of oxazoline ligands

doi:10.1016/S0010-8545(99)00086-7

Paper

Coordination chemistry of oxazoline ligands

Published Oct 1, 1999 · M. Gómez, G. Muller, Mercè Rocamora

Coordination Chemistry Reviews

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170

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Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

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Study Snapshot

Oxazoline ligands offer versatility in ligand design, straightforward synthesis, and modulation of chiral centers for transition metal-catalyzed asymmetric organic syntheses.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Paper

Coordination chemistry of oxazoline ligands

References

Citations

Doubly Metathetic NiCl2-Catalyzed Coupling Between Bis(2-oxazolines) and Aldehydes: A Novel Access to Bis(ester-imine) Derivatives

NiCl2-catalyzed coupling between bis(2-oxazolines) and aromatic aldehydes produces useful bis(ester-imine) derivatives in synthetically useful yields.

Heteroaromatic N-Oxides Modified with a Chiral Oxazoline Moiety, Synthesis and Catalytic Applications

Chiral oxazoline substituted pyridine N-oxides show potential as catalysts for allylation of benzaldehyde and nitroaldol reaction, with up to 79% effective efficiency.

4,4-Bis(hydroxymethyl)-2-phenyl-2-oxazoline

This study successfully resynthesised 4,4-bis(hydroxymethyl)-2-phenyl-2-oxazoline in high yields, revealing its structure and interactions through H-bonds.

Self-Healing and Moldable Poly(2-isopropenyl-2-oxazoline) Supramolecular Hydrogels Based on a Transient Metal Coordination Network

Self-healing and moldable poly(2-isopropenyl-2-oxazoline) supramolecular hydrogels with metal coordination show potential for applications in robotics, coatings, and wound healing.

Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes

This study successfully prepared tetraorganotin tin(IV) compounds with flexible or rigid oxazoline functionality, leading to stable polystannanes and oligostannanes through dihydride conversion and DFT studies.

KOt-Bu-promoted selective ring-opening N-alkylation of 2-oxazolines to access 2-aminoethyl acetates and N-substituted thiazolidinones

This study presents a simple and efficient method for synthesis of versatile 2-aminoethyl acetates and N-substituted thiazolidinones with good functional group tolerance and selectivity using KOt-Bu as an oxygen donor.