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Acetophenone chloroborane

The nopol derivative (5) has advantages in some cases but the most striking advance has been the introduction of commercially available chloroborane (6). Compound (6) is a stronger Lewis acid than (4) or (5) and also less subject to steric hindrance. It readily reduces acetophenone (98% ee),... [Pg.603]

Girard, C., Kagan, H. B. 1995. Nonlinear effects in the reduction of acetophenone by diisopinocampheyl chloroborane Influence of the reagent preparation. Tetrahedron Asymmetry 6 1881-1884. [Pg.619]

See other pages where Acetophenone chloroborane is mentioned: [Pg.194]    [Pg.25]   
See also in sourсe #XX -- [ Pg.603 ]

See also in sourсe #XX -- [ Pg.603 ]

See also in sourсe #XX -- [ Pg.7 , Pg.603 ]

See also in sourсe #XX -- [ Pg.7 , Pg.603 ]

See also in sourсe #XX -- [ Pg.603 ]



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