1131004-45-9Relevant articles and documents
Copper-catalyzed cross-coupling reaction of organoboron compounds with primary alkyl halides and pseudohalides
Yang, Chu-Ting,Zhang, Zhen-Qi,Liu, Yu-Chen,Liu, Lei
, p. 3904 - 3907 (2011/05/15)
Non-activated alkyl electrophiles, including alkyl iodides, bromides, tosylates, mesylates, and even chlorides, underwent copper-catalyzed cross-coupling with aryl boron compounds and alkyl 9-BBN reagents (see scheme; 9-BBN=9-borabicyclo[3.3.1]nonane). The reactions proceed with practically useful reactivities and thus complement palladium- and nickel-catalyzed Suzuki-Miyaura coupling reactions of alkyl halides.
Domino iron catalysis: Direct aryl-alkyl cross-coupling
Czaplik, Waldemar Maximilian,Mayer, Matthias,Von Wangelin, Axel Jacobi
supporting information; experimental part, p. 607 - 610 (2009/04/14)
(Chemical Equation Presented) Striking while the iron is hot: Cheap FeCl3 serves as the precatalyst for the direct cross-coupling of aryl and alkyl halides that is based on the sequence of Grignard formation and subsequent cross-coupling. This