23418-91-9Relevant articles and documents
DYNAMIC NMR SPECTROSCOPY OF THE TETRAVALENT ORGANOBORATE COMPOUNDS. SYNTHESIS AND SOME UNIQUE FEATURES OF ORGANOBORATES CONTAINING THE C6H4CH2NMe2-2 LIGAND
Kalbarczyk, E.,Pasynkiewicz, S.
, p. 119 - 132 (1985)
Novel borates (ArBMe3)Li*OEt2 (I), (ArBEt)Li*OEt2 (II) and (BArPh-9-BBn)Li*OEt2 (III) (Ar=C6H4NMe2-2, 9-BBN=9-borabicyclononyl) were synthesized in the reactions of ArLi with BMe3, BEt3 and BPh-9-BBN, respectively.Detailed studies were made of 1H,
Palladium-catalyzed 1,3-diol fragmentation: Synthesis of ω-dienyl aldehydes
Kimura, Masanari,Mori, Masahiko,Tamaru, Yoshinao
, p. 4504 - 4506 (2007)
2-(1′-Hydroxy-2′-propenyl)cycloalkan-1-ols 1 undergo dehydrative C1-C2 bond cleavage and provide ω-dienyl aldehydes 2 under the catalysis of Pd(0) and 9-phenyl-9-BBN. The Royal Society of Chemistry.
New Method for the Synthesis of Organoboranes
Whiteley, Chris G.
, p. 5 - 6 (1981)
Mixed organoboranes can be conveniently prepared in a single stage by treatment of a dialkylborane with various lithium dialkyl- or diaryl-cuprates.
Suzuki-miyaura cross-coupling reactions of unactivated alkyl halides catalyzed by a nickel pincer complex
Di Franco, Thomas,Boutin, Nicolas,Hu, Xile
, p. 2949 - 2958 (2013/11/06)
A nickel(II) pincer complex, [(MeN2N)Ni-Cl], was used to catalyze alkyl-alkyl and alkyl-aryl Suzuki-Miyaura coupling reactions of unactivated alkyl halides. The coupling of 9-alkyl-9-borabicyclo[3.3.1]nonane and 9-phenyl-9-borabicyclo[3.3.1]nonane reagents with alkyl halides was achieved in modest to good yields. The reactions tolerated a variety of useful functional groups including ester, ether, furan, thioether, acetal, and Boc groups. Georg Thieme Verlag Stuttgart, New York.