1.3 C—H Bond Functionalization
Book
Editors: Cazin, C. ; Nolan, S.
Title: N-Heterocyclic Carbenes in Catalytic Organic Synthesis 1
Print ISBN: 9783132012813; Online ISBN: 9783132407633; Book DOI: 10.1055/b-004-132254
1st edition © 2017. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry
Science of Synthesis Reference Libraries
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: Carreira, E. M.; Decicco, C. P.; Fürstner, A.; Koch, G.; Molander, G.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.
Type: Multivolume Edition
Abstract
This chapter deals with C—H bond functionalization catalyzed by N-heterocyclic carbene transition-metal complexes. The C—H bond functionalizations have been classified with respect to the hybridization of the carbon atom and the reaction type.
Key words
C—H bonds - metal–carbene complexes - ligands - imidazoles - imidazolylidenes - N-heterocyclic carbenes- 7 Fructos, MR, de Frémont, P, Nolan, SP, Díaz-Requejo, MM, Pérez, PJ. Organometallics. 2006; 25: 2237
- 9 Hashmi, ASK, Braun, I, Nösel, P, Schädlich, J, Wieteck, M, Rudolph, M, Rominger, F. Angew. Chem. Int. Ed.. 2012; 51: 4456
- 10 Wieteck, M, Tokimizu, Y, Rudolph, M, Rominger, F, Ohno, H, Fujii, N, Hashmi, ASK. Chem.–Eur. J.. 2014; 20: 16331
- 11 Barluenga, J, Sigüeiro, R, Vicente, R, Ballesteros, A, Tomás, M, Rodríguez, MA. Angew. Chem. Int. Ed.. 2012; 51: 10377
- 20 Marion, N, Ecarnot, EC, Navarro, O, Amoroso, D, Bell, A, Nolan, SP. J. Org. Chem.. 2006; 71: 3816
- 24 Lavallo, V, Canac, Y, Präsang, C, Donnadieu, B, Bertrand, G. Angew. Chem. Int. Ed.. 2005; 44: 5705
- 34 Jia, Y.-X, Hillgren, JM, Watson, EL, Marsden, SP, Kündig, EP. Chem. Commun. (Cambridge). 2008; 4040
- 44 To, W.-P, Tong, GS.-M, Lu, W, Ma, C, Liu, J, Chow, AL.-F, Che, C.-M. Angew. Chem. Int. Ed.. 2012; 51: 2654
- 46 Renaudat, A, Jean-Gérard, L, Jazzar, R, Kefalidis, CE, Clot, E, Baudoin, O. Angew. Chem. Int. Ed.. 2010; 49: 7261
- 50 Fructos, MR, Belderrain, TR, de Frémont, P, Scott, NM, Nolan, SP, Díaz-Requejo, MM, Pérez, PJ. Angew. Chem. Int. Ed.. 2005; 44: 5284
- 51 Rivilla, I, Gómez-Emeterio, BP, Fructos, MR, Díaz-Requejo, MM, Pérez, PJ. Organometallics. 2011; 30: 2855
- 55 Hoshimoto, Y, Hayashi, Y, Suzuki, H, Ohashi, M, Ogoshi, S. Angew. Chem. Int. Ed.. 2012; 51: 10812
- 75 Azpíroz, R, Di Giuseppe, A, Castarlenas, R, Pérez-Torrente, JJ, Oro, LA. Chem.–Eur. J.. 2013; 19: 3812
- 76 Azpíroz, R, Rubio-Pérez, L, Di Giuseppe, A, Passarelli, V, Lahoz, FJ, Castarlenas, R, Pérez-Torrente, JJ, Oro, LA. ACS Catal.. 2014; 4: 4244
- 77 Rubio-Pérez, L, Azpíroz, R, Di Giuseppe, A, Polo, V, Castarlenas, R, Pérez-Torrente, JJ, Oro, LA. Chem.–Eur. J.. 2013; 19: 15304
- 81 Brown, JA, Irvine, S, Kennedy, AR, Kerr, WJ, Andersson, S, Nilsson, GN. Chem. Commun. (Cambridge). 2008; 1115
- 82 Cochrane, AR, Idziak, C, Kerr, WJ, Mondal, B, Paterson, LC, Tuttle, T, Andersson, S, Nilsson, GN. Org. Biomol. Chem.. 2014; 12: 3598
- 83 Brown, JA, Cochrane, AR, Irvine, S, Kerr, WJ, Mondal, B, Parkinson, JA, Paterson, LC, Reid, M, Tuttle, T, Andersson, S, Nilsson, GN. Adv. Synth. Catal.. 2014; 356: 3551