Direct synthesis of a geminal zwitterionic phosphonium/hydridoborate system – developing an alternative tool for generating frustrated Lewis pair hydrogen activation systems†,10.1039/C5OB00634A

热搜：

Lactoyl-CoA 全氟丁基戊烷白叶藤碱全氟己基辛烷新白叶藤碱壳寡糖特色专题-生物多肽

Direct synthesis of a geminal zwitterionic phosphonium/hydridoborate system – developing an alternative tool for generating frustrated Lewis pair hydrogen activation systems†

Jiangang Yu,Gerald Kehr,Constantin G. Daniliuc,Christoph Bannwarth,Stefan Grimme,Gerhard Erker

Organic & Biomolecular Chemistry Pub Date : 04/15/2015 00:00:00 , DOI:10.1039/C5OB00634A

Abstract

A convenient way to a new class of geminal Mes₂PH⁺/B(C₆F₅)₂H⁻ pairs is presented. It utilizes triflic acid addition to trans-Mes₂PCH [double bond, length as m-dash] CHB(C₆F₅)₂ followed by triflate/hydride exchange. Thermally induced ring-closure gave a phosphonium/boratacyclopropane zwitterion 8 which formed the Mes₂PH(CHMe)B(C₆F₅)₂H P/B FLP-H₂ product 10 by subsequent treatment with triflic acid and a silane, or alternatively with dihydrogen at 90 °C. The product 10 is an active catalyst for the hydrogenation of a variety of unsaturated organic substrates, including a quinoline derivative. Treatment of compound 8 with HB(C₆F₅)₂ gave a bifunctional borane 14 which selectively reduced carbon monoxide to the formyl stage.