ASYMMETRIC SYNTHESIS XXⅧ:ENANTIOSELECTIVE REDUCTION OF AROMATIC KETONES CATALYZED BY NEW CHIRAL CATALYST-(4R,8R,9S)-CAMPHANE[8,9-b]-1,3,2-OXATHIOBOROLIDINE

Yao Zhong Jiang Xiao Ming Feng Liu Zhu Gong Zhi Li Gui Su Yang Ai Qiao Mi

引用本文: Yao Zhong Jiang,  Xiao Ming Feng,  Liu Zhu Gong,  Zhi Li,  Gui Su Yang,  Ai Qiao Mi. ASYMMETRIC SYNTHESIS XXⅧ:ENANTIOSELECTIVE REDUCTION OF AROMATIC KETONES CATALYZED BY NEW CHIRAL CATALYST-(4R,8R,9S)-CAMPHANE[8,9-b]-1,3,2-OXATHIOBOROLIDINE[J]. Chinese Chemical Letters, 1996, 7(5): 415-418. shu
Citation:  Yao Zhong Jiang,  Xiao Ming Feng,  Liu Zhu Gong,  Zhi Li,  Gui Su Yang,  Ai Qiao Mi. ASYMMETRIC SYNTHESIS XXⅧ:ENANTIOSELECTIVE REDUCTION OF AROMATIC KETONES CATALYZED BY NEW CHIRAL CATALYST-(4R,8R,9S)-CAMPHANE[8,9-b]-1,3,2-OXATHIOBOROLIDINE[J]. Chinese Chemical Letters, 1996, 7(5): 415-418. shu

ASYMMETRIC SYNTHESIS XXⅧ:ENANTIOSELECTIVE REDUCTION OF AROMATIC KETONES CATALYZED BY NEW CHIRAL CATALYST-(4R,8R,9S)-CAMPHANE[8,9-b]-1,3,2-OXATHIOBOROLIDINE

摘要: (4R,8R,9S)-Camphane[8,9-b]-1,3,2-oxathioborolidine prepared from (1R,2S,3R)-3-mercapto-camphol with borane was used as catalyst in the enantioselective reduction of aromatic ketones:moderate enantioselectivities with e.e.7.44%-51.04% have been obtained for aromatic ketones with 20% mol catalyst,73.78% e.e for ω-bromo acetophenone with 100% mol catalyst.

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  • 收稿日期:  1995-10-13
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