71089-15-1Relevant academic research and scientific papers
Nickel-catalyzed cross-coupling reactions of alkyl aryl sulfides and alkenyl alkyl sulfides with alkyl grignard reagents using (Z)-3,3-dimethyl-1,2- bis(diphenylphosphino)but-1-ene as ligand
Kanemura, Shigenari,Kondoh, Azusa,Yorimitsu, Hideki,Oshima, Koichiro
scheme or table, p. 2659 - 2664 (2009/04/05)
A combination of nickel(II) acetylacetonate and (Z)-3,3-dimethyl-1,2- bis(diphenylphosphino)but-1-ene catalyzes cross-coupling reactions of alkyl aryl sulfides and alkenyl alkyl sulfides with alkyl Grignard reagents. Not only primary but also secondary alkyl Grignard reagents can be employed. Georg Thieme Verlag Stuttgart.
Mildly and highly selective reductive deoxygenation of para-di- and monoalkylaminophenyl ketones by borane
Wei, Tiezheng,Lan, Yu,Xu, Jiaxi
, p. 2 - 5 (2007/10/03)
Para-di- and monoalkylaminophenyl ketones were reduced selectively to para-alkyl N, N-di- and N-monoalkylanilines in good to excellent yields by borane under mild, convenient, and neutral conditions.
Benzotriazole-mediated synthesis of α-di- and α-trisubstituted ethers and sulfides
Katritzky,Jurczyk,Szajda,Shcherbakova,Lam
, p. 499 - 504 (2007/10/02)
Ethylaryl- and diethylaryl(benzotriazol-1-yl)methanes, obtained by mono- or dialkylation of substituted (benzotriazol-1-ylmethyl)benzenes, react with sodium alkoxides, phenol and thiophenol to yield the corresponding α-di- and α-trisubstituted ethers and
