Divergent g-C3N4-catalyzed Reactions of Quinoxalin-2(1H)-ones with N-Aryl Glycines under Visible Light: Solvent-Controlled Hydroaminomethylation and Annulation
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DOI: 10.1021/acssuschemeng.0c02289
Abstract: An effective and simple visible light-induced heterogeneous g-C3N4-catalyzed decarboxylative reaction of quinoxalin-2(1H)-ones with N-aryl glycines was developed. When the reaction was performed in... read more here.
Keywords: c3n4 catalyzed; ones aryl; aryl glycines; visible light ... See more keywords
Visible-light-promoted decarboxylative addition cyclization of N-aryl glycines and azobenzenes to access 1,2,4-triazolidines
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DOI: 10.1039/d1gc02272e
Abstract: Direct synthesis of 1,2,4-triazolidines have been readily achieved by the visible-light-promoted reaction of N-aryl glycines and azobenzenes under mild conditions. read more here.
Keywords: aryl glycines; visible light; glycines azobenzenes; promoted decarboxylative ... See more keywords
N-Aryl glycines as versatile initiators for various polymerizations
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DOI: 10.1039/d1py00030f
Abstract: The design and development of versatile initiators for various types of polymerization reactions, i.e. thermal-/photo-crosslinked/controlled polymerizations, is highly interesting to fabricate high-performance polymer materials. Herein, we synthesized two N-aryl glycine-based initiators, N-(1-naphthyl)glycine (NNG) and N-(1-pyrenyl)glycine… read more here.
Keywords: aryl glycines; glycines versatile; various polymerizations; versatile initiators ... See more keywords
A mild and efficient synthesis of N-aryl glycines by the rearrangement of 2-chloro-N-aryl acetamides
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DOI: 10.1039/d5ra02497h
Abstract: A mild and efficient one-pot procedure was developed for the synthesis of substituted N-aryl glycines from 2-chloro-N-aryl acetamides by intermolecular cyclization in the presence of CuCl2ยท2H2O and KOH under reflux condition in acetonitrile medium. The… read more here.
Keywords: aryl glycines; aryl acetamides; mild efficient; chloro aryl ... See more keywords