Journal
CHEMICAL COMMUNICATIONS
Volume 57, Issue 60, Pages 7414-7417Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc02602j
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An azopyridine-based oxazoline ligand was developed for utilizing azo group coordination and isomerization as a photoswitchable ligand, enabling modulation of the enantioselectivity of an RE-catalyzed aminal forming reaction through efficient E/Z photoisomerization.
An azopyridine-based oxazoline was developed for utilizing azo group coordination and isomerization as a photoswitchable ligand. The ligand coordinated to rare-earth metal (RE) catalyst underwent efficient E/Z photoisomerization, suggesting tri- and bidentate coordination switching. The photoisomerization of the ligand enabled modulation of the enantioselectivity of an RE-catalyzed aminal forming reaction.
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