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Functionalized acyclic alkenes halides

Borabicyclo[3.3.1]nonane (9-BBN) has found use in the selective hydro-boration of alkenes in the presence of other reducible functional groups and its reaction with alkynylstannates has been studied. o-Stannyl- and a-silyl-substituted crotyl-9-BBN show promise as reagents for the stereo-regulated synthesis of acyclic systems. A series of papers covers the question of olefin-alkyl exchange in. 5-alkyl-9-BBN s, " the kinetics of reduction of substituted benzaldehydes with 9-BBN, and the kinetics and mechanism of hydroboration of alkynes with 9-BBN dimers. Selective dehalogenation of tertiary alkyl, benzyl, and allyl halides in the presence of secondary or primary alkyl or aryl halides is possible with (165). The... [Pg.465]


See other pages where Functionalized acyclic alkenes halides is mentioned: [Pg.1116]    [Pg.1116]    [Pg.131]    [Pg.131]    [Pg.16]    [Pg.382]    [Pg.424]    [Pg.452]    [Pg.43]    [Pg.1887]    [Pg.184]    [Pg.383]   
See also in sourсe #XX -- [ Pg.145 ]




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