1313872-22-8Relevant academic research and scientific papers
Highly functional group compatible Rh-catalyzed addition of arylboroxines to activated N-tert-butanesulfinyl ketimines
Jung, Hyung Hoon,Buesking, Andrew W.,Ellman, Jonathan A.
supporting information; experimental part, p. 3912 - 3915 (2011/09/16)
The rhodium-catalyzed addition of readily accessible arylboroxines to N-tert-butanesulfinyl ketimines derived from oxetan-3-one, N-Boc-azetidin-3-one, and isatins proceeds in high yields with excellent functional group compatibility. Moreover, high diastereoselectivities are observed for the additions to the N-sulfinyl ketimines derived from isatins.
Grignard addition to imines derived from isatine: A method for the asymmetric synthesis of quaternary 3-aminooxindoles
Lesma, Giordano,Landoni, Nicola,Pilati, Tullio,Sacchetti, Alessandro,Silvani, Alessandra
experimental part, p. 4537 - 4541 (2009/09/30)
(Chemical Equation Presented) Addition of Grignard reagents to chiral imines derived from isatine afforded chiral, optically enriched 3-substituted 3-aminooxindoles in satisfactory yields and diastereoisomeric ratios. A general protocol is described for t
