733810-61-2Relevant academic research and scientific papers
Amino alcohols as ligands for nickel-catalyzed Suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids
Gonzalez-Bobes, Francisco,Fu, Gregory C.
, p. 5360 - 5361 (2007/10/03)
Suzuki cross-coupling reactions of an unprecedented array of unactivated primary and secondary alkyl halides (including challenging alkyl chlorides) can be accomplished through the use of nickel/amino alcohol-based catalysts. Both the nickel precatalyst and the amino alcohols (prolinol or trans-2-aminocyclohexanol) are commercially available and air-stable. In view of the remarkable diversity of amino alcohols that are readily accessible, this discovery may open the door to the rapid development of versatile catalysts for a wide range of cross-coupling processes. Copyright
Nickel-catalyzed cross-couplings of organosilicon reagents with unactivated secondary alkyl bromides
Powell, David A.,Fu, Gregory C.
, p. 7788 - 7789 (2007/10/03)
A metal-catalyzed cross-coupling of organosilicon compounds with alkyl halides has been developed. Noteworthy attributes of the method are its scope (secondary electrophiles), its high functional-group compatibility, and the air stability of the catalyst components. Copyright
