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Alkali metal catalyzed dehydro-coupling of boranes and amines leading to the formation of a B–N bond

机译:碱金属催化硼烷和胺的脱氢偶联,导致B-N键的形成

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In this report we describe catalytic B–N bond formation via cross-dehydrocoupling (CDC) of boranes with amines to construct aminoboranes with a high degree conversion (>90%) and chemo-selectivity using alkali metal hexamethyldisilazides [MN(SiMe _(3) ) _(2) ] (M = Li, and K) as pre-catalysts. It was observed that the lithium and potassium hexamethyldisilazides proved to be an effective pre-catalyst for aliphatic primary, secondary amines, aromatic primary, and substituted amines. The catalyzed cross-dehydrocoupling reaction using [MN(SiMe _(3) ) _(2) ] (M = Li and K) as a pre-catalyst displayed a broad substrate scope. Pinacolborane smoothly reacted with a number of aliphatic and aromatic amines under ambient conditions whereas a prolonged reaction time of around 8–12 hours was required for 9-BBN to undergo CDC reactions.
机译:在本报告中,我们通过甘氨酸的交叉脱水耦合(CDC)描述催化B-N键形成,所述胺用高度转化(> 90%)和使用碱金属六甲基二酶[Mn(Sime _(3 ))_(2)](m = li,k)作为预催化剂。观察到锂和己酰基甲基二酶被证明是脂族初级,仲胺,芳族初级和取代胺的有效前催化剂。使用[Mn(SIME _(3))_(2)](M = Li和K)作为预催化剂的催化交叉脱氢耦合反应显示宽底物范围。 Pinacolborane在环境条件下与许多脂族和芳族胺平滑地反应,而9-BBN需要延长的反应时间约为8-12小时以进行CDC反应。

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