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[21][24] We wish to report herein our synthetic approach toward -hydroxyamino ketones, which involves the radical acylation of nitrone with 2-acylbenzothiazolene under organophotoredox catalysis (route C). Metal- and Additive-Free Synthesis of -Hydroxyamino Ketones Enabled by Organophotocatalyst Hydroxyamino ketone, hydroxylamine, nitrone, benzothiazoline, metal-free, organophotocatalyst Keywords: hydroxyamino ketone; hydroxylamine; nitrone; benzothiazoline; organophotocatalyst; metal-free EN hydroxyamino ketone hydroxylamine nitrone benzothiazoline organophotocatalyst metal-free 1391 1394 4 07/11/23 20230725 NES 230725 Graph Nitrogen-containing compounds are prevalent in organic compounds, and a range of novel catalytic approaches have been extensively explored. [Extracted from the article]

The high-yield reduction of aromatic ketimines into amines by using a novel catalyst based on a metallacarborane structure, 8,8'-μ-phosphate[(1,2-dicarba-closo-undecaborane)-3,3'-cobalt(- 1)(1',2'-dicarba-closo-undecaborane)] acid, is described. [ABSTRACT FROM AUTHOR]

A novel chiral phosphoric acid bearing a biphenol backbone was synthesized and its catalytic activity was investigated in the enantioselective Mannich-type reaction of ketene silyl acetals with aldimines. [ABSTRACT FROM AUTHOR]

A novel chiral phosphoric acid bearing a biphenol backbone was synthesized and its catalytic activity was investigated in the enantioselective Mannich-type reaction of ketene silyl acetals with aldimines. [ABSTRACT FROM AUTHOR]

A new approach is described for the asymmetric synthesis of 1-substituted 1,2,3,4-tetrahydroisoquinolines that is based on the enantioselective 1,3-dipolar cycloaddition reaction of a nitrone and a vinyl ether in the presence of a chiral phosphoric acid that gives the chiral tetrahydroisoquinolines in high yields and with high enantioselectivities.1 H and31 P NMR analyses of the mixture of nitrone and chiral phosphoric acid suggest the formation of a 1:1 complex. [ABSTRACT FROM AUTHOR]

The metal-free reduction of nitroarenes to aniline derivatives was accomplished in a short time by using a benzothiazoline as the hydrogen donor in combination with a Brønsted acid. An enantioselective synthesis of 2-arylquinolines was achieved by using 1-aryl-3-(2-nitrophenyl)propan-1-ones as starting materials and a combination of a benzothiazoline and a chiral phosphoric acid. [ABSTRACT FROM AUTHOR]