Banert, K. et al.: 2013 Science of Synthesis, 2013/2: Knowledge Updates 2013/2 DOI: 10.1055/sos-SD-101-00153
Knowledge Updates 2013/2

1.2.6 High-Valent Palladium in Catalysis

More Information

Book

Editors: Banert, K.; Drabowicz, J.; Oestreich, M.; Plietker, B. J.; Ramsden, C.; Schaumann, E.; Stoltz, B. M.; Weinreb, S. M.

Authors: Baumgartner, J.; Chen, P.; Durand, A.; Engle, K. M.; Hayashi, M.; Hemeon, I.; Kawachi, A.; Liu, G.; Louie, J.; Marschner, C.; Nahra, F.; Pietrusiewicz, K. M.; Podlech, J.; Riant, O.; Santi, C.; Scammells, P. J.; Shimada, K.; Singer, R. D.; Stankevič, M.; Stolley, R. M.; Yu, J.-Q.; Zhang, J.

Title: Knowledge Updates 2013/2

Print ISBN: 9783131727619; Online ISBN: 9783132401440; Book DOI: 10.1055/b-003-128236

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry

Science of Synthesis Knowledge Updates



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Carreira, E. M.; Decicco, C. P.; Fürstner, A.; Molander, G. A.; Reider, P. J.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.

Type: Multivolume Edition

 


Abstract

This chapter documents recent studies of palladium-catalyzed organic transformations in which a high-valent palladium intermediate is involved in the formation of a new chemical bond. The interest in these reactions has focused mainly on C—H activation and the difunctionalization of alkenes.

 
  • 1 Tsuji J. Palladium Reagents and Catalysis: New Perspectives for the 21st Century. Wiley; Chichester, UK 2004
  • 3 Metal-Catalyzed Cross-Coupling Reactions. de Meijere A, Diederich F. Wiley-VCH; Weinheim, Germany 2004
  • 9 Racowski JM, Sanford MS, Topics in Organometallic Chemistry. Canty AJ. Springer; Berlin 2011. 35. 61
  • 11 Eberson L, Jönsson L. Justus Liebigs Ann. Chem. 1977; 233
  • 13 Byers PK, Canty AJ, Skelton BW, White AH. J. Chem. Soc., Chem. Commun. 1986; 1722
  • 15 Canty AJ. Dalton Trans. 2009; 10 409
  • 27 Oloo W, Zavalij PY, Zhang J, Khaskin E, Vedernikov AN. J. Am. Chem. Soc. 2010; 132: 14 400
  • 29 Penno D, Lillo V, Koshevoy IO, Sanaú M, Ubeda MA, Lahuerta P, Fernández E. Chem.–Eur. J. 2008; 14: 10 648
  • 32 Cotton FA, Koshevoy IO, Lahuerta P, Murillo CA, Sanaú M, Ubeda MA, Zhao Q. J. Am. Chem. Soc. 2006; 128: 13 674
  • 35 Powers DC, Benitez D, Tkatchouk E, Goddard III WA, Ritter T. J. Am. Chem. Soc. 2010; 132: 14 092
  • 36 Powers DC, Lee E, Ariafard A, Sanford MS, Yates BF, Canty AJ, Ritter T. J. Am. Chem. Soc. 2012; 134: 12 002
  • 50 Catellani M, Motti E, Minari M. Chem. Commun. (Cambridge) 2000; 157
  • 51 Catellani M. Synlett 2003; 298
  • 54 Maestri G, Motti E, Della Ca’ N, Malacria M, Derat E, Catellani M. J. Am. Chem. Soc. 2011; 133: 8574
  • 61 Zhao Y.-B, Mariampillai B, Candito DA, Laleu B, Li MZ, Lautens M. Angew. Chem. Int. Ed. 2009; 48: 1849
  • 89 Jordan-Hore JA, Johansson CCC, Gulias M, Beck EM, Gaunt MJ. J. Am. Chem. Soc. 2008; 130: 16 184
  • 96 Giri R, Maugel N, Li J.-J, Wang D.-H, Breazzano SP, Saunders LB, Yu J.-Q. J. Am. Chem. Soc. 2007; 129: 3510
  • 99 Constable AG, McDonald WS, Sawkins LC, Shaw BL. J. Chem. Soc., Chem. Commun. 1978; 1061
  • 100 Baldwin JE, Nájera C, Yus M. J. Chem. Soc., Chem. Commun. 1985; 126
  • 106 Zhang J, Khaskin E, Anderson NP, Zavalij PY, Vedernikov AN. Chem. Commun. (Cambridge) 2008; 3625
  • 107 Giri R, Liang J, Lei J.-G, Li J.-J, Wang D.-H, Chen X, Naggar IC, Cuo C, Foxman BM, Yu J.-Q. Angew. Chem. Int. Ed. 2005; 44: 7420
  • 118 Hövelmann CH, Streuff J, Brelot L, Muñiz K. Chem. Commun. (Cambridge) 2008; 2334
  • 122 Chen S, Wu T, Liu G, Zhen X. Synlett 2011; 891
  • 132 Stangl H, Jira R. Tetrahedron Lett. 1970; 3589
  • 146 Tsujihara T, Takenaka K, Onitsuka K, Hatanaka M, Sasai H. J. Am. Chem. Soc. 2009; 131: 3452
  • 148 Jaegli S, Dufour J, Wei H.-L, Piou T, Duan X.-H, Vors J.-P, Neuville L, Zhu J. Org. Lett. 2010; 12: 4498