Organisch-Chemisches Institut der Universität Münster, Corrensstrasse 40, 48149 Münster (Germany).
Angew Chem Int Ed Engl. 2014 Jan 20;53(4):1118-21. doi: 10.1002/anie.201307551. Epub 2013 Dec 11.
Boranes R2 BH react with carbon monoxide by forming the respective borane carbonyl compounds R2 BH(CO). The formation of (C6 F5 )2 BH(CO) derived from the Piers borane, HB(C6 F5 )2 , is a typical example. Subsequent CO-hydroboration does not take place, since the formation of the formylborane is usually endothermic. However, an "η(2) -formylborane" was formed by CO-hydroboration with the Piers borane at vicinal phosphane/borane frustrated Lewis pair (FLP) templates. Subsequent treatment with pyridine liberated the intact formylborane from the FLP framework, and (pyridine)(C6 F5 )2 BCHO was then isolated as a stable compound. This product underwent typical reactions of carbonyl compounds, such as Wittig olefination.
硼烷 R2BH 与一氧化碳反应,形成相应的硼烷羰基化合物 R2BH(CO)。由 Piers 硼烷 HB(C6F5)2 衍生而来的 (C6F5)2BH(CO)的形成就是一个典型的例子。由于甲酰硼烷的形成通常是吸热的,因此不会发生随后的 CO 氢硼化反应。然而,在相邻膦/硼受阻路易斯对 (FLP)模板的作用下,用 Piers 硼烷进行 CO 氢硼化反应生成了“η(2)-甲酰硼烷”。随后用吡啶处理,将完整的甲酰硼烷从 FLP 骨架中释放出来,然后将 (吡啶)(C6F5)2BCHO 作为稳定化合物分离出来。该产物经历了羰基化合物的典型反应,如 Wittig 烯烃化反应。