1247014-68-1Relevant academic research and scientific papers
Alkenylborane-derived frustrated Lewis pairs: Metal-free catalytic hydrogenation reactions of electron-deficient alkenes
Reddy, J. Sreedhar,Xu, Bao-Hua,Mahdi, Tayseer,Froehlich, Roland,Kehr, Gerald,Stephan, Douglas W.,Erker, Gerhard
, p. 5638 - 5649 (2012/11/13)
A series of alkenylboranes were prepared by 1,1-carboboration routes and used as Lewis acid components for the generation of frustrated Lewis pairs (FLPs). The reactions of 1-alkynes with B(C6F5) 3 gave the RCH=C(C6F5)B(C6F 5)2 systems 4a(R = n-C3H7), 4b (R = n-C4H9), 4c (R = Ph), and 4d (R = t-C4H 9), respectively. The alkenylborane/tBu3P FLPs derived from compounds 4a-d reacted rapidly with dihydrogen (2.5 bar) at ambient temperature. The bulky system 4d left the C=C double bond of the alkenylborane unsaturated and gave the dihydrogen cleavage product [tBu3PH][tBuCH= C(C6F5)BH(C6F5)2] (10d). In contrast, the less bulky systems 4a/tBu3P and 4b/tBu3P split dihydrogen under these conditions and had their C=C double bonds cleanly reduced to yield the corresponding 1-pentafluorophenylalkyl hydridoborate salts [tBu3PH][RCH2CH(C6F5)BH(C 6F5)2] 9a (R = n-C3H7) and 9b (R = n-C4H9), respectively. The 4c/tBu3P FLP gave a mixture of both product types (9c/10c). 1,1-Carboboration of symmetrical internal alkynes gave the alkenylboranes R2C=C(C 6F5)B(C6F5)24e (R = C2H5), 4f (R = n-C3H7), 4g (R = Ph), and 4h (R = p-MeC6H4), respectively. The 4e-h/tBu 3P FLPs cleaved dihydrogen under mild conditions but retained their C=C double bonds to give the respective [tBu3PH][R 2C=C(C6F5)BH(C6F5) 2] products (10e-h). Selected examples of these alkenylboranes undergo FLP reactions acting as catalysts for the hydrogenation of imines. Perhaps most remarkably, some of these alkenylboranes retain the C=C double bonds under FLP/H2 reaction conditions and heterolytically split dihydrogen in the presence of the Lewis base DABCO and catalyze the hydrogenation of the electron-poor C=C double bonds of diaryl-substituted enones.
Carbon-carbon bond activation by 1,1-carboboration of internal alkynes
Chen, Chao,Kehr, Gerald,Froehlich, Roland,Erker, Gerhard
supporting information; experimental part, p. 13594 - 13595 (2010/11/18)
Internal alkynes undergo 1,1-carboboration reactions upon treatment with boranes RB(C6F5)2 (R = C6F 5, CH3) to yield trisubstituted alkenylboranes. These products can be used as substrates
