Fig. 1: Background and new strategy to access S-chirogenic sulfinamides. | Nature Communications

Fig. 1: Background and new strategy to access S-chirogenic sulfinamides.

From: Asymmetric reductive arylation and alkenylation to access S-chirogenic sulfinamides

Fig. 1

a Reaction diversity of S-chirogenic sulfinamides. b Asymmetric synthesis of chiral sulfinyl compounds by organocatalysts. c Metal-catalysed synthesis of S-chirogenic sulfinamides using arylboron compounds. d Reported results on asymmetric reductive addition for constructing chiral C − C bonds. e Asymmetric reductive addition of aryl and alkenyl halides to sulfinylamines to form C − S bonds.

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