All articles of this category Regioselective silaboration of 3-substituted 1,2-dienes was efficiently catalyzed by palladium/2,6-xylyl isocyanide complex, affording an adduct, in which the boryl and silyl groups were introduced at the central allenyl carbon and at the substituted allenyl carbon, respectively. silaboration - allenes - palladium/2,6-xylyl isocyanide - regioselectivity - 2-boryl allylsilane
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Suginome et al. (1999) studied this question.