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Acetylene haloboration

Stereoselective addition of B-Br across a terminal acetylene (haloboration) was first reported by Blackborow (66). Suzuki and coworkers examined the intermediate obtained from the haloboration of alkynes with B-bromo and 5-iodo-9-borabicyclo[3.3.1]nonanes for various organoborane reactions. Suzuki has reviewed the applications of haloboration for organic syntheses (67-69). A recent application involving the 1,4-addition of a halovinyl-9-BBN to methyl vinyl ketone (70) for the synthesis of a promising anti-cancer agent, 12,13-desoxyepothilone B due to Danishefsky and coworkers is shown in Figure 19 (77). [Pg.14]

B-Bromo and B-iodo-9-borabicyclo[3.3.1]nonane add similarly in a cis fashion to terminal triple bonds 471 They do not react, however, with alkenes and internal acetylenic bonds. In contrast to the results mentioned above, phenyl-substituted chloroboranes (PhBCl2, Ph2BCl) do not participate in haloboration. Instead, the C—B bond adds across the multiple bond to form phenylalkyl-(alkenyl) boranes.466,468... [Pg.328]

Haloboranes add to terminal alkynes in a cis /in-Markovnikov manner however, the bromoboration of acetylene itself exceptionally provides a trans adduct [28] (eq (17)). A sequence of haloboration with boron tribromide and then cross-coupling with organozincs is useful for a formal carboboration of alkynes with various organic groups. Addition of boron triboromide to allene is convenient for the synthesis of (2-bromo-2-propeny])borate [29] (eq (18)). [Pg.349]

Boron tribromide has also been used as a haloboration reagent, in particular by Suzuki and CO workers For instance, they reacted it with terminal acetylenes and subsequently converted the monoaddition product to a 1,2-dihalo-1 -alkene. Since the addition proceeds regio- and stereoselectively and the halogenation occurs with retention, the 1,2-dihalo products have the (Z)-configuration. Oxidation of the addition product by 30% hydrogen peroxide in a solution buffered at pH 5 and in the presence of potassium acetate afforded a 2-bromoalkanaE A combination of halo- and hydroboration was applied in a one-pot... [Pg.903]


See other pages where Acetylene haloboration is mentioned: [Pg.156]    [Pg.157]    [Pg.285]    [Pg.272]    [Pg.61]    [Pg.54]    [Pg.611]    [Pg.48]    [Pg.410]   
See also in sourсe #XX -- [ Pg.328 ]




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