Enantioselective Rh-Catalyzed Arylation of N-Tosylarylimines with Arylboronic Acids
摘要:
The asymmetric arylation of N-tosylarylimines with arylboronic acids was realized by using rhodium/(S)-ShiP as catalyst. The reaction proceeded in aqueous toluene to give diarylmethylamines in good yields with up to 96% ee.
Annunziata, Rita; Cinquini, Mauro; Cozzi, Franco, Journal of the Chemical Society. Perkin transactions I, 1982, p. 339 - 344
作者:Annunziata, Rita、Cinquini, Mauro、Cozzi, Franco
DOI:——
日期:——
Lead Tetraacetate Cleavage of Chiral Phenylglycinol Derived Secondary Amines Without Racemization
作者:Mohamed K. Mokhallalati、Lendon N. Pridgen
DOI:10.1080/00397919308009866
日期:1993.7
Diastereomerically enriched N-(1,1-disubstituted methyl)(2-hydroxy-1'-phenylethyl)amines were oxidatively converted to enantiomerically enriched primary disubstituted methylamines in excellent yields without racemization, using an improved lead tetraacetate (LTA) procedure.
Asymmetric Synthesis of Diarylmethyl Amines by Rhodium-Catalyzed Asymmetric Addition of Aryl Titanium Reagents to Imines
作者:Tamio Hayashi、Masahiro Kawai、Norihito Tokunaga
DOI:10.1002/anie.200461338
日期:2004.11.19
Enantioselective Rh-Catalyzed Arylation of <i>N</i>-Tosylarylimines with Arylboronic Acids
The asymmetric arylation of N-tosylarylimines with arylboronic acids was realized by using rhodium/(S)-ShiP as catalyst. The reaction proceeded in aqueous toluene to give diarylmethylamines in good yields with up to 96% ee.