Axially Dissymmetric Chiral (R)‐N,W‐Bis(2‐hydroxy‐3,5‐ditert‐butyl‐arylmethyl)‐1, 1′‐binaphthalene‐2,2′‐diamine as Chiral Ligands in the Reaction of Diethylzinc to Aldehydes† |
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Authors: | Min Shi Wei‐Liang Duan Guo‐Bin Rong |
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Abstract: | Chiral ligand (A)‐N,N′‐Bis(2‐hydroxy‐3,5‐di‐tert‐butyl‐arylmethyl)‐1,1′‐binaphthalene‐2,2′‐diamine derived from the reduction of Schiff base (R)‐2,2′‐bis (3,5‐di‐tert‐butyl‐2‐hydroxybenzylideneamino)‐1, 1′‐binaphthyl with LiAlH4, is fairly effective in the asymmetric addition reaction of diethylzinc to aldehydes by which good yields (46%‐94%) of the corresponding sec‐alcohols can be obtained in moderate ee (51%‐79%) with R configuration for a variety of aldehydes. |
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Keywords: | axially dissymmetric chiral ligand (R)‐N N′ ‐bis(2‐hydroxy‐3,5‐di‐tert‐butyl‐arylmethyl)‐1 1′ ‐binaphthalene‐2,2′ ‐diamine diethylzinc asymmetric addition reaction |
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