Advances in functional-group-tolerant metal-catalyzed alkyl-alkyl cross-coupling reactions

Angewandte Chemie - International Edition

Volumn 42, Issue 4, 2003, Pages 384-387

  Càrdenas, Diego J ^a  

^a UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

Alkanes; Boranes; Cross coupling; Nickel; Palladium

Indexed keywords

CARBON; CATALYST ACTIVITY; CHEMICAL BONDS; REACTION KINETICS;

CROSS-COUPLING REACTIONS;

ORGANOMETALLICS;

1,3 BUTADIENE; AMIDE; BORANE DERIVATIVE; BROMIDE; ETHER DERIVATIVE; HALIDE; ISOPRENE; KETONE DERIVATIVE; METAL COMPLEX; NICKEL COMPLEX; NITRILE; ORGANOMETALLIC COMPOUND; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON; STYRENE DERIVATIVE; SULFONIC ACID DERIVATIVE; TOLUENESULFONIC ACID DERIVATIVE; ZINC COMPLEX;

ALKYLATION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL BOND; CHEMICAL REACTION; CROSS COUPLING REACTION; LOW TEMPERATURE; OXIDATION REDUCTION REACTION;

EID: 0037468071     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200390123     Document Type: Article

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34. The oxidative addition mechanism involved in this case is different. Some leading references on aryl chlorides functionalization: a) J. P. Wolfe, R. A. Singer, B. H. Yang, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9550-9561; b) A. F. Littke, L. Schwarz, G. C. Fu, J. Am. Chem. Soc. 2002, 124, 6343-6348; c) A. F. Littke, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 6989-7000; d) A. Furstner, A. Leitner, Synlett 2001, 290-292.
35. The oxidative addition mechanism involved in this case is different. Some leading references on aryl chlorides functionalization: a) J. P. Wolfe, R. A. Singer, B. H. Yang, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9550-9561; b) A. F. Littke, L. Schwarz, G. C. Fu, J. Am. Chem. Soc. 2002, 124, 6343-6348; c) A. F. Littke, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 6989-7000; d) A. Furstner, A. Leitner, Synlett 2001, 290-292.
36. The oxidative addition mechanism involved in this case is different. Some leading references on aryl chlorides functionalization: a) J. P. Wolfe, R. A. Singer, B. H. Yang, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9550-9561; b) A. F. Littke, L. Schwarz, G. C. Fu, J. Am. Chem. Soc. 2002, 124, 6343-6348; c) A. F. Littke, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 6989-7000; d) A. Furstner, A. Leitner, Synlett 2001, 290-292.
37. The oxidative addition mechanism involved in this case is different. Some leading references on aryl chlorides functionalization: a) J. P. Wolfe, R. A. Singer, B. H. Yang, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9550-9561; b) A. F. Littke, L. Schwarz, G. C. Fu, J. Am. Chem. Soc. 2002, 124, 6343-6348; c) A. F. Littke, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 6989-7000; d) A. Furstner, A. Leitner, Synlett 2001, 290-292.