Cazin, C.  et al.: 2017 Science of Synthesis, 2016/5a: N-Heterocyclic Carbenes in Catalytic Organic Synthesis 1 DOI: 10.1055/sos-SD-223-00179
N-Heterocyclic Carbenes in Catalytic Organic Synthesis

1.4.5 Hydroamination

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Book

Editors: Cazin, C. ; Nolan, S.

Authors: Albrecht, M.; Baudrenghien, L.; Bielawski, C.; Biffis, A.; Cavallo, L.; Cazin, C. ; César, V.; Chetcuti, M.; Cuenca, A.; de Frémont, P.; Elie, M.; Fairlamb, I.; Falivene, L.; Fernandez Gutierrez, M. E.; Gagné, M. R.; Gaillard, S.; Huynh, H.; Kalck, P.; Kuwano, R.; Lastovickova, D.; Lavigne, G.; Makida, Y.; Marko, I.; Martin, A.; Nahra, F. ; Nakao, Y.; Ogasawara, M. ; Payne, P.; Renaud, J.; Ronson, T.; Ruamps, M.; Segarra Almela, C.; Teator, A.; Trzeciak, A.; Tubaro, C.; Urrutigoity, M.; Vummaleti, S.; Whittlesey, M.; Yuan, D.

Title: N-Heterocyclic Carbenes in Catalytic Organic Synthesis 1

Print ISBN: 9783132012813; Online ISBN: 9783132407633; Book DOI: 10.1055/b-004-132254

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

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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

Hydroamination, the addition of an N—H moiety across carbon–carbon unsaturation, is an attractive, atom-economical methodology for the synthesis of nitrogen-containing compounds. N-Heterocyclic and cyclic (alkyl)(amino)carbenes have been applied as supporting ligands for the synthesis of catalysts capable of mediating both inter- and intramolecular (cyclization) reactions with alkynes, allenes, and activated alkenes.

 
  • 2 Müller, TE, Hultzsch, KC, Yus, M, Foubelo, F, Tada, M. Chem. Rev.. 2008; 108: 3795
  • 3 Severin, R, Doye, S. Chem. Soc. Rev.. 2007; 36: 1407
  • 4 Yim, JC.-H, Schafer, LL. Eur. J. Org. Chem.. 2014; 6825
  • 5 Aillaud, I, Collin, J, Hannedouche, J, Schulz, E. Dalton Trans.. 2007; 5105
  • 6 Hannedouche, J, Schulz, E. Chem.–Eur. J.. 2013; 19: 4972
  • 7 Reznichenko, AL, Hultzsch, KC, In Chiral Amine Synthesis. Nugent, TC, ED. Wiley-VCH Weinheim, Germany 2010; p 341
  • 10 Hong, S, Marks, TJ. Acc. Chem. Res.. 2004; 37: 673
  • 11 Reznichenko, AL, Hultzsch, KC. Top. Organomet. Chem.. 2013; 43: 51
  • 13 Bytschkov, I, Doye, S. Eur. J. Org. Chem.. 2003; 935
  • 14 Huang, L, Arndt, M, Gooßen, K, Heydt, H, Gooßen, LJ. Chem. Rev.. 2015; 115: 2596
  • 15 Nishina, N, Yamamoto, Y. Top. Organomet. Chem.. 2013; 43: 115
  • 16 Hesp, KD, Stradiotto, M. ChemCatChem. 2010; 2: 1192
  • 17 Kumar, A, Ghosh, P. Eur. J. Inorg. Chem.. 2012; 3955
  • 18 Walsh, PJ, Baranger, AM, Bergman, RG. J. Am. Chem. Soc.. 1992; 114: 1708
  • 19 Senn, HM, Blöchl, PE, Togni, A. J. Am. Chem. Soc.. 2000; 122: 4098
  • 20 Casalnuovo, AL, Calabrese, JC, Milstein, D. J. Am. Chem. Soc.. 1988; 110: 6738
  • 21 Widenhoefer, RA, Han, X. Eur. J. Org. Chem.. 2006; 4555
  • 22 Seligson, AL, Trogler, WC. Organometallics. 1993; 12: 744
  • 23 Pouy, MJ, Delp, SA, Uddin, J, Ramdeen, VM, Cochrane, NA, Fortman, GC, Gunnoe, TB, Cundari, TR, Sabat, M, Myers, WH. ACS Catal.. 2012; 2: 2182
  • 24 Gray, K, Page, MJ, Wagler, J, Messerle, BA. Organometallics. 2012; 31: 6270
  • 25 Schaper, L.-A, Wei, X, Hock, SJ, Pöthig, A, Öfele, K, Cokoja, M, Herrmann, WA, Kühn, FE. Organometallics. 2013; 32: 3376
  • 26 Field, LD, Messerle, BA, Vuong, KQ, Turner, P. Organometallics. 2005; 24: 4241
  • 27 Ackermann, L, Sandmann, R, Schinkel, M, Kondrashov, MV. Tetrahedron. 2009; 65: 8930
  • 28 Michon, C, Medina, F, Abadie, M.-A, Agbossou-Niedercorn, F. Organometallics. 2013; 32: 5589
  • 29 Li, H, Widenhoefer, RA. Org. Lett.. 2009; 11: 2671
  • 30 Clark, WD, Cho, J, Valle, HU, Hollis, TK, Valente, EJ. J. Organomet. Chem.. 2014; 751: 534
  • 31 Arrowsmith, M, Hill, MS, Kociok-Köhn, G. Organometallics. 2009; 28: 1730
  • 32 Zhang, R, Xu, Q, Mei, L.-Y, Li, S.-K, Shi, M. Tetrahedron. 2012; 68: 3172
  • 33 Bender, CF, Widenhoefer, RA. Org. Lett.. 2006; 8: 5303
  • 34 Lavallo, V, Frey, GD, Donnadieu, B, Soleilhavoup, M, Bertrand, G. Angew. Chem. Int. Ed.. 2008; 47: 5224
  • 35 Zeng, X, Frey, GD, Kousar, S, Bertrand, G. Chem.–Eur. J.. 2009; 15: 3056
  • 36 Dash, C, Shaikh, MM, Butcher, RJ, Ghosh, P. Inorg. Chem.. 2010; 49: 4972
  • 37 López-Gómez, MJ, Martin, D, Bertrand, G. Chem. Commun. (Cambridge). 2013; 49: 4483
  • 38 Manzano, R, Wurm, T, Rominger, F, Hashmi, ASK. Chem.–Eur. J.. 2014; 20: 6844
  • 39 Chen, Q, Lv, L, Yu, M, Shi, Y, Li, Y, Pang, G, Cao, C. RSC Adv.. 2013; 3: 18359
  • 40 Guo, P, Zeng, X, Chen, S, Luo, M. J. Organomet. Chem.. 2014; 751: 438
  • 41 Liu, X.-Y, Ding, P, Huang, J.-S, Che, C.-M. Org. Lett.. 2007; 9: 2645
  • 42 Zeng, X, Frey, GD, Kinjo, R, Donnadieu, B, Bertrand, G. J. Am. Chem. Soc.. 2009; 131: 8690
  • 43 Kinder, RE, Zhang, Z, Widenhoefer, RA. Org. Lett.. 2008; 10: 3157
  • 44 Zeng, X, Soleilhavoup, M, Bertrand, G. Org. Lett.. 2009; 11: 3166
  • 45 Munro-Leighton, C, Delp, SA, Blue, ED, Gunnoe, TB. Organometallics. 2007; 26: 1483
  • 46 Houghton, J, Dyson, G, Douthwaite, RE, Whitwood, AC, Kariuki, BM. Dalton Trans.. 2007; 3065
  • 47 Gischig, S, Togni, A. Eur. J. Inorg. Chem.. 2005; 4745
  • 48 Dash, C, Shaikh, MM, Butcher, RJ, Ghosh, P. Dalton Trans.. 2010; 39: 2515
  • 49 Cao, P, Cabrera, J, Padilla, R, Serra, D, Rominger, F, Limbach, M. Organometallics. 2012; 31: 921