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Carbon polyboranes

While alkynes, nitriles, and isocyanides have long been known to insert a cage carbon into polyboranes (COMC (1982) 5.4.2.6.1 and 5.4.2.6.2), the use of aldehydes to insert a cage carbon was first reported by Bernd Brellochs in 1997 (Figure 5).86 Good yields of 10-vertex monocarbaboranes were obtained from B10H14 with KOH and many aldehydes and this reaction was thus coined the Brellochs reaction. 87... [Pg.53]

Diborane is not unique among the boron hydrides in its ability to form a carbonyl. High pressure reaction of either pentaborane-f / or tetra-borane-10 with carbon monoxide forms a substance which behaves like borane-carbonyl in its manner of decomposition. The formula of this polyborane-carbonyl has recently been established as OC B Hg (mp, — 114.5° bp, 59.6°) 41a). It reacts with trimethylamine without release of carbon monoxide. [Pg.301]


See other pages where Carbon polyboranes is mentioned: [Pg.156]    [Pg.458]    [Pg.203]    [Pg.272]    [Pg.497]    [Pg.21]    [Pg.124]    [Pg.160]    [Pg.234]    [Pg.270]    [Pg.171]    [Pg.172]    [Pg.215]    [Pg.497]    [Pg.24]    [Pg.43]    [Pg.23]    [Pg.68]    [Pg.22]    [Pg.850]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.5 , Pg.7 , Pg.10 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.5 , Pg.7 ]




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Polyborane

Polyboranes

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