Artigo Revisado por pares

Hindered organoboron groups in organic synthesis. 17 [1]. Synthesis of 2,4,6‐triisopropylphenylborane (TripBH 2 ) 2 , a useful alternative to thexylborane

1992; Wiley; Volume: 3; Issue: 3 Linguagem: Inglês

10.1002/hc.520030313

ISSN

1098-1071

Autores

Andrew Pelter, Keith Smith, D. BUSS, Jin Zhao,

Tópico(s)

Chemical Synthesis and Reactions

Resumo

Abstract 2,4,6‐Triisopropylphenylborane (tripylborane, TripBH 2 ) resembles thexylborane in having a single, bulky organic group attached to boron, but the group is aromatic rather than aliphatic. The compound has been synthesized by two alternative routes, one involving direct reduction of dimethoxytripylborane and the other involving redistribution between ditripylborane and borane. It is a solid which is considerably more stable than thexylborane.

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