143592-79-4Relevant academic research and scientific papers
Organosubstituted cis-1,2-Diborylalkenes as Electrophilic Chelates
Koester, Roland,Seidel, Guenter,Wagner, Klaus,Wrackmeyer, Bernd
, p. 305 - 318 (2007/10/02)
Triethylborane (1), 9-ethyl-9-borabicyclononane (9-ethyl-9-BBN) (2), and the cis-1,2-diborylalkenes (Z)-R2BC(R')=C(Et)BEt2 react with alkali metal salts MX in toluene to give the borates MX-1, MX-2, and the cyclic cis-1,2-diborates , resp., with BHB- and B(OR)B-bridges (IR, Multi NMR).Reaction of 1, 2, and 3 - 6 with KCN leads to the monoborates KCN-1, KCN-2, and to the acyclic cis-1,2-diborates KCN-3 to KCN-7. - The cis-2-Boryl-1-silylalkenes (E)-Me3SiC(R')=C(Et)BEt2 and KX form the acyclic borates K.The cyclic salts KOtBu-4 and KOSiEt3-4 undergo a B-substituent exchange to the acyclic cis-1,2-diborates K (K-10: R = tBu; K-11: R = OSiEt3).Key Words: cis-1,2-Diborylalkenes, electron acceptors, anion sponge / Diborates, hexaorgano, μ-hydro, μ-alkoxy, alkali metal salts / Borates, hydrotriorgano- / Substituent exchange, diborates
