References
- Sahakitpichan , P. , Thasana , N. and Ruchirawat , S. 2005 . Efficient synthesis of diospyrol via Suzuki–Miyaura and modified in situ cross‐coupling . Synthesis , 17 : 2934 – 2938 .
- Roschangar , F. , Brown , J. C. , Cooley , B. E. , Sharp , M. J. and Matsuoka , R. T. 2002 . Use of lithium N,O‐dimethylhydroxylamide as an efficient in situ protecting agent for aromatic aldehydes . Tetrahedron , 58 ( 9 ) : 1657 – 1666 .
- McClure , M. S. , Roschangar , F. , Hodson , S. J. , Millar , A. and Osterhout , M. H. 2001 . A practical one‐pot synthesis of 5‐aryl‐2‐furaldehydes . Synthesis , 11 : 1681 – 1685 .
- Ferreira , I. C. F. R. , Queiroz , M.‐J. R. P. and Kirsch , G. 2001 . Synthesis of new methylated thieno[2,3‐a] and [3,2‐b]carbazoles by reductive cyclization of 6‐(2′‐nitrophenyl)benzo[b]thiophenes obtained by palladium‐catalyzed cross‐coupling . J. Heterocycl. Chem. , 38 ( 3 ) : 749 – 754 .
- Passafaro , M. S. and Keay , B. A. 1996 . A one pot in situ combined Shapiro‐Suzuki reaction . Tetrahedron Lett. , 37 ( 4 ) : 429 – 432 .
- Baudoin , O. , Guénard , D. and Guéritte , F. 2000 . Palladium‐catalyzed borylation of ortho‐substituted phenyl halides and application to the one‐pot synthesis of 2,2′‐disubstituted biphenyls . J. Org. Chem. , 65 : 9268 – 9271 .
- Ferreira , I. C. F. R. , Queiroz , M.‐J. R. P. and Kirsch , G. 2003 . Tandem palladium‐catalyzed borylation and Suzuki coupling (BSC) to thienocarbazole precursors . Tetrahedron Lett. , 44 ( 23 ) : 4327 – 4329 .
- Giroux , A. , Han , Y. and Prasit , P. 1997 . One pot biaryl synthesis via in situ boronate formation . Tetrahedron Lett. , 38 : 3841 – 3844 .
- Ishiyama , T. , Itoh , Y. , Kitano , T. and Miyaura , N. 1997 . Synthesis of arylboronates via the palladium(0)‐catalyzed cross‐coupling reaction of tetra(alkoxo)diborons with aryl triflates . Tetrahedron Lett. , 38 : 3447 – 3450 .
- Miura , M. , Koike , T. , Ishihara , T. , Hirayama , F. , Sakamoto , S. , Okada , M. , Ohta , M. and Tsukamoto , S. 2006 . A one‐pot synthetic procedure for 2,2′‐disubstituted biaryls via Suzuki coupling reaction of aryl triflates in a biphasic solvent system . Synth. Commun. , 36 : 3809 – 3820 .
- Castanet , A.‐S. , Colobert , F. , Desmurs , J.‐R. and Schlama , S. J. 2002 . Biaryl synthesis via Suzuki coupling promoted by catalytic amounts of quaternary ammonium salts . J. Mol. Catal. , 182–183 : 481 – 487 .
- Paetzold , E. , Jovel , I. and Oehme , G. 2004 . Suzuki reactions in aqueous multi‐phase systems promoted by supported detergents . J. Mol. Catal. A: Chem. , 214 ( 2 ) : 241 – 247 .
- Christoforou , I. C. , Koutentis , P. A. and Rees , C. W. 2003 . Regiospecific Suzuki coupling of 3,5‐dichloroisothiazole‐4‐carbonitrile . Org. Biomol. Chem. , 1 ( 16 ) : 2900 – 2907 .
- Segelstein , B. E. , Butler , T. W. and Chenard , B. L. 1995 . Equilibration of the oxidative addition product of tetrakis(triphenylphosphine)palladium and electron‐donating aryl halides leads to product scrambling in the Stille reaction . J. Org. Chem. , 60 ( 1 ) : 12 – 13 .
- Grifftiths , C. and Leadbeater , N.E. 2004 . Palladium and nickel catalysed Suzuki cross‐coupling of sterically hindered aryl bromides with phenylboronic acid . Tetrahedron Lett. , 41 : 2487 – 2490 . For the cross‐coupling of sterically hindered aryl halides, see, for example
- Lourak , M. , Vanderesse , R. , Fort , Y. and Caubere , P. 1989 . Activation of reducing agents: Sodium hydride containing complex reducing agents, 32: NiCRALs as very efficient agents in promoting cross‐coupling of aryl halides . J. Org. Chem. , 54 ( 20 ) : 4844 – 4848 .
- Burawoy , A. and Spinner , E. 1955 . Electronic spectra of organic molecules and their interpretation, part I. Effect of terminal methyl and substituted methyl groups of conjugated systems on K‐bands . J. Chem. Soc. , : 2557 – 2563 .
- Denmark , S. E. and Ober , M. H. 2003 . Cross‐coupling reactions of arylsilanols with substituted aryl halides . Org. Lett. , 5 ( 8 ) : 1357 – 1360 .