Does 9-BBN not act on internal alkynes or alkenes?

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9-BBN's steric hindrance raises questions about its reactivity with internal alkynes and alkenes for hydroboration. While some sources suggest that 9-BBN can react with internal alkenes, it is anticipated that the reaction rate would be slower compared to terminal alkenes. The design of 9-BBN, featuring larger substituents, aims to promote boron addition at less hindered sites, enhancing regioselectivity. Compared to borane-THF, 9-BBN is noted for its greater regioselectivity, and its availability in solid form offers practical advantages over gaseous B2H6.
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Organic Chemistry question! Is 9-BBN too sterically hindered to even react with internal alkynes or alkenes? (to do hydroboration)
 
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I've seen claims that 9-BBN can react with internal alkenes, but I haven't attempted it myself. I imagine the reaction would take longer than a reaction with a terminal alkene. The goal of the big substituents is to favor boron addition at less sterically hindered sites with high regioselectivity. 9-BBN generally tends to be more regioselective than something like borane-THF. You can also get it in solid form, which is easier to use than gaseous B2H6.
 
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