Palladium-catalyzed cross-coupling of cyclopropylmagnesium bromide with aryl bromides mediated by zinc halide additives.
Chutian Shu, Kanwar Sidhu, Li Zhang, Xiao-Jun Wang, Dhileepkumar Krishnamurthy, Chris H Senanayake
Index: J. Org. Chem. 75(19) , 6677-80, (2010)
Full Text: HTML
Abstract
The key Pd-catalyzed cross-coupling of aryl bromides or triflates and cyclopropylmagnesium bromide in the presence of substoichiometric amounts of zinc bromide produces cyclopropyl arenes in good to excellent yields. The cross-coupling of other alkyl, cycloalkyl, and aryl Grignard reagents with aryl bromides under the same conditions gives the corresponding substituted arenes in good yields.
Related Compounds
Related Articles:
Asymmetric Rh-catalyzed intermolecular hydroacylation of 1,5-hexadiene with salicylaldehyde.
2009-10-01
[Chem. Pharm. Bull. 57(10) , 1158-60, (2009)]
2011-08-16
[Chemistry 17(34) , 9385-94, (2011)]
Stereoselective glycosylations using benzoylated glucosyl halides with inexpensive promoters.
2008-06-09
[Carbohydr. Res. 343(8) , 1297-308, (2008)]
[Halogenated anesthetic vaporizers: importance of maintenance regulations].
1998-01-01
[Ann. Fr. Anesth. Reanim. 17(7) , 747-9, (1998)]
2000-07-01
[Chem. Pharm. Bull. 48(7) , 1097-100, (2000)]