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Cyclopentylmagnesium bromide

CuHtsNOj 13118-11-1) see Glycopyrronium bromide cyclopentylideneacetonitrile (C7H9N 5732-88-7) see Cyclopentamine cyclopentylmagnesium bromide... [Pg.2341]

The last step of the synthesis is a reductive amination of a ketone that is formed by oxidation of the corresponding alcohol. The alcohol results from the Grignard reaction between cyclopentylmagnesium bromide and propylene oxide. [Pg.673]

Using cyclopentylmagnesium bromide, cyclohexylmagnesium bromide, cycloheptyl-magnesium bromide, benzylmagnesium bromide, or 2-phenylethylmagnesium bromide rather than isopropylmagnesium bromide in this sequence led to a variety of... [Pg.215]

See other pages where Cyclopentylmagnesium bromide is mentioned: [Pg.57]    [Pg.76]    [Pg.4]    [Pg.20]    [Pg.834]    [Pg.1261]    [Pg.203]    [Pg.228]    [Pg.375]    [Pg.584]    [Pg.824]    [Pg.1265]    [Pg.1018]    [Pg.136]    [Pg.190]    [Pg.375]    [Pg.57]    [Pg.76]    [Pg.4]    [Pg.20]    [Pg.834]    [Pg.1261]    [Pg.203]    [Pg.228]    [Pg.375]    [Pg.584]    [Pg.824]    [Pg.1265]    [Pg.1018]    [Pg.136]    [Pg.190]    [Pg.375]    [Pg.185]    [Pg.29]    [Pg.22]    [Pg.22]    [Pg.582]    [Pg.616]    [Pg.240]   
See also in sourсe #XX -- [ Pg.190 ]



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