Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bin-Hua Yuan"'
Publikováno v:
Journal of Saudi Chemical Society, Vol 22, Iss 6, Pp 654-664 (2018)
An Efficient method for the syntheses of N-tert-butanesulfinyl aldimines in water was developed using Amberlyst-15 as catalyst. Subsequently, chiral homoallylic amines were synthesized in one pot from aldehydes by combining with In-promoted allylatio
Externí odkaz:
https://doaj.org/article/343df1b4cab040efb8b17d502784923f
Publikováno v:
Tetrahedron Letters. 57:2147-2151
The first access to chiral homoallylic–homopropargylic amine bearing two contiguous stereocenters has been well accomplished via zinc-promoted aza-Barbier reaction. N-tert-Butanesulfinyl ketimines are well-tolerated substrates, providing the tertia
Publikováno v:
Organicbiomolecular chemistry. 16(1)
Highly stereoselective syntheses of chiral indolines and tetrahydroquinolines are achieved by combining the asymmetric Zn-mediated allylation of chiral N-tert-butanesulfinyl imines with efficient intramolecular C–N cross-coupling. Herein, the advan
Publikováno v:
Chemical communications (Cambridge, England). 53(25)
Highly diastereoselective palladium catalyzed cinnamylation of N-tert-butanesulfinyl imines with cinnamyl acetates has been established to provide enantioenriched β-aryl homoallylic amines. The synthetic application of this stragety has been success
Publikováno v:
ChemInform. 47
The first access to chiral homoallylic–homopropargylic amine bearing two contiguous stereocenters has been well accomplished via zinc-promoted aza-Barbier reaction. N-tert-Butanesulfinyl ketimines are well-tolerated substrates, providing the tertia
Publikováno v:
ChemInform. 44
A highly efficient method for the asymmetric synthesis of chiral quaternary carbon-containing homoallylic and homopropargylic amines under mild conditions was achieved with good yields and high diastereoselectivities.
Publikováno v:
Chinese Journal of Organic Chemistry. 36:1308
Publikováno v:
Chemical Communications. 49:5402
A highly efficient method for the asymmetric synthesis of chiral quaternary carbon-containing homoallylic and homopropargylic amines under mild conditions was achieved with good yields and high diastereoselectivities.