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Cinnamyl alcohol solid support

The relatively inexpensive and safe sodium borohydride (NaBH4) has been extensively used as a reducing agent because of its compatibility with protic solvents. Varma and coworkers reported a method for the expeditious reduction of aldehydes and ketones that used alumina-supported NaBH4 and proceeded in the solid state accelerated by microwave irradiation (Scheme 7) [50]. The chemoselectivity was apparent from the reduction of frarcs-cinnamaldehyde to afford cinnamyl alcohol. [Pg.210]

Solid-support-bound 1-aminoimidazolium chlorochromate 82 proved to be a selective oxidant for benzylic and cinnamylic alcohols <01S382>. Imidazolyl-A -difluoromethyltrimethylsilanes 83 are versatile sources of heteroaryl-A -difluoromethyl anions in reactions with carbonyl compounds <01SL374>. [Pg.189]

See other pages where Cinnamyl alcohol solid support is mentioned: [Pg.281]   
See also in sourсe #XX -- [ Pg.841 ]

See also in sourсe #XX -- [ Pg.841 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.841 ]



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Alcohol, solid

Alcohols solid support

Cinnamyl alcohol

Solid support

Solid-supported

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