FULL PAPERS
c) Comprehensive Asymmetric Catalysis; (Eds.: E. N.
Jacobsen, A. Pfaltz, H. Yamamoto), Springer-Verlag,
Berlin, 1999; d) Asymmetric Catalysis in Organic Syn-
thesis, (Ed.: R. Noyori),Wiley, New York, 1994; e) Ap-
plied Homogeneous Catalysis with Organometallic
Compounds, 2nd edn., (Eds.: B. Cornils, W. A. Herr-
mann), Wiley-VCH, Weinheim, 2002.
5817; b) S. Zhou, S. Fleischer, K. Junge, S. Das, D.
Addis, M. Beller, Angew. Chem. 2010, 122, 8298–8302;
Angew. Chem. Int. Ed. 2010, 49, 8121–8125; c) A. A.
Mikhailine, R. H. Morris, Inorg. Chem. 2010, 49,
11039–11044; d) A. Naik, T. Maji, O. Reiser, Chem.
Commun. 2010, 46, 4475–4477; e) A. Mikhailine, A. L.
Lough, R. H. Morris, J. Am. Chem. Soc. 2009, 131,
1394–1395.
[2] a) Modern Reduction Methods, (Eds.: P. G. Andersson,
I. J. Munslow), Wiley-VCH, Weinheim, 2008; b) X. Wu,
C. Wang, J. Xiao, Platinum Met. Rev. 2010, 54, 3–19;
c) C. Wang, X. Wu, J. Xiao, Chem. Asian J. 2008, 3,
1750–1770; d) T. Ikariya, A. J. Blacker, Acc. Chem. Res.
2007, 40, 1300–1308; e) S. Gladiali, E. Alberico, Chem.
Soc. Rev. 2006, 35, 226–236; f) K. Everaere, A. Mor-
treux, J.-F. Carpentier, Adv. Synth. Catal. 2003, 345, 67–
77; g) T. Ohkuma, R. Noyori, in: Comprehensive Asym-
metric Catalysis, Vol. 1, (Eds.: E. N. Jacobsen, A. Pfaltz,
H. Yamamoto), Springer, Berlin, 1999, p 199; h) M. J.
Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10,
2045–2061; i) R. Noyori, S. Hashiguchi, Acc. Chem.
Res. 1997, 30, 97–102; j) G. Zassinovich, G. Mestroni, S.
Gladiali, Chem. Rev. 1992, 92, 1051–1069; k) J. S. M.
Samec, J.-E. Bꢈckvall, P. G. Andersson, P. Brandt,
Chem. Soc. Rev. 2006, 35, 237–248; l) J. Margalef, O.
Pꢂmies, M. Diꢁguez, Tetrahedron Lett. 2016, 57, 1301–
1308; m) F. Foubelo, C. Najera, M. Yus, Tetrahedron:
Asymmetry 2015, 26, 769–790; n) D. Wang, D. Astruc,
Chem. Rev. 2015, 115, 6621–6686.
[3] For example, see: a) S. Hashiguchi, A. Fujii, J. Take-
hara, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995,
117, 7562–7563; b) A. Fujii, S. Hashiguchi, H. Uematsu,
T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1996, 118,
2521–2522; c) D. A. Alonso, D. Guijarro, P. Pinho, O.
Temme, P. G. Andersson, J. Org. Chem. 1998, 63, 2749–
2751; d) J. Hannedouche, G. J. Clarkson, M. Wills, J.
Am. Chem. Soc. 2004, 126, 986–987; e) W. Baratta, G.
Chelucci, E. Herdtweck, S. Magnolia, K. Siega, P. Rigo,
Angew. Chem. 2007, 119, 7795–7798; Angew. Chem.
Int. Ed. 2007, 46, 7651–7654; f) T. C. Johnson, W. G.
Totty, M. Wills, Org. Lett. 2012, 14, 5230–5233; g) W.
Baratta, F. Benedetti, A. Del Zotto, L. Fanfoni, F. Fell-
uga, S. Magnolia, E. Putignano, P. Rigo, Organometal-
lics 2010, 29, 3563–3570.
[8] For example, see: a) S. J. Nordin, P. Roth, T. Tarnai,
D. A. Alonso, P. Brandt, P. G. Andersson, Chem. Eur. J.
2001, 7, 1431–1436; b) D. A. Alonso, S. J. Nordin, P.
Roth, T. Tarnai, P. G. Andersson, M. Thommen, U. Pit-
telkow, J. Org. Chem. 2000, 65, 3116–3122; c) A. Schlat-
ter, W.-D. Woggon, Adv. Synth. Catal. 2008, 350, 995–
1000; d) A. Schlatter, M. K. Kundu, W.-D. Woggon,
Angew. Chem. 2004, 116, 6899–6902; Angew. Chem.
Int. Ed. 2004, 43, 6731–6734; e) D. S. Matharu, D. J.
Morris, A. M. Kawamoto, G. J. Clarkson, M. Wills, Org.
Lett. 2005, 7, 5489–5491; f) F. K. Cheung, C. Lin, F.
Minissi, A. L. Crivillꢁ, M. A. Graham, D. J. Fox, M.
Wills, Org. Lett. 2007, 9, 4659–4662; g) V. Parekh, J. A.
Ramsden, M. Wills, Catal. Sci. Technol. 2012, 2, 406–
414.
[9] M. T. Reetz, X. Li, J. Am. Chem. Soc. 2006, 128, 1044–
1051.
[10] W. Ye, M. Zhao, Z. Yu, Chem. Eur. J. 2012, 18, 10843–
10846.
[11] a) I. M. Pastor, P. Vꢈstilꢈ, H. Adolfsson, Chem. Eur. J.
2003, 9, 4031–4045; b) A. Bøgevig, I. M. Pastor, H.
Adolfsson, Chem. Eur. J. 2004, 10, 294–300; c) P. Vꢈsti-
lꢈ, J. Wettergren, H. Adolfsson, Chem. Commun. 2005,
4039–4041; d) J. Wettergren, A. Bøgevig, M. Portier, H.
Adolfsson, Adv. Synth. Catal. 2006, 348, 1277–1282;
e) P. Vꢈstilꢈ, A. B. Zaitsev, J. Wettergren, T. Privalov,
H. Adolfsson, Chem. Eur. J. 2006, 12, 3218–3225; f) J.
Wettergren, A. B. Zaitsev, H. Adolfsson, Adv. Synth.
Catal. 2007, 349, 2556–2562; g) J. Wettergren, E. Buitra-
go, P. Ryberg, H. Adolfsson, Chem. Eur. J. 2009, 15,
5709–5713; h) K. Ahlford, J. Ekstrçm, A. B. Zaitsev, P.
Ryberg, L. Eriksson, H. Adolfsson, Chem. Eur. J. 2009,
15, 11197–11205; i) F. Tinnis, H. Adolfsson, Org.
Biomol. Chem. 2010, 8, 4536–4539; j) K. Ahlford, M.
Livendahl, H. Adolfsson, Tetrahedron Lett. 2009, 50,
6321–6324; k) M. Coll, K. Ahlford, O. Pꢂmies, H.
Adolfsson, M. Diꢁguez, Adv. Synth. Catal. 2012, 354,
415–427; l) I. M. Pastor, P. Vꢈstilꢈ, H. Adolfsson,
Chem. Commun. 2002, 2046–2047; m) A. B. Zaitsev, H.
Adolfsson, Org. Lett. 2006, 8, 5129–5132.
[4] For example, see: a) K. Murata, T. Ikariya, R. Noyori,
J. Org. Chem. 1999, 64, 2186–2187; b) T. Thorpe, J.
Blacker, S. M. Brown, C. Bubert, J. Crosby, S. Fitzjohn,
J. P. Muxworthy, J. M. J. Williams, Tetrahedron Lett.
2001, 42, 4041–4043; c) G. Dyson, J.-C. Frison, A. C.
Whitwood, R. E. Douthwaite, Dalton Trans. 2009,
7141–7151; d) A. Aupoix, C. Bournaud, G. Vo-Thanh,
Eur. J. Org. Chem. 2011, 2772–2776.
[5] See also: a) Z.-R. Dong, Y.-Y. Li, J.-S. Chen, B.-Z. Li,
Y. Xing, J.-X. Gao, Org. Lett. 2005, 7, 1043–1045;
b) D. G. I. Petra, P. C. J. Kamer, A. L. Spek, H. E.
Schoemaker, P. W. N. M. van Leeuwen, J. Org. Chem.
2000, 65, 3010–3017.
[12] M. Coll, O. Pꢂmies, H. Adolfsson, M. Diꢁguez, Chem.
Commun. 2011, 47, 12188–12190.
[13] M. Coll, O. Pꢂmies, H. Adolfsson, M. Diꢁguez, Chem-
CatChem 2013, 5, 3821–3828.
[14] C. Matassini, S. Mirabella, A. Goti, F. Cardona, Eur. J.
Org. Chem. 2012, 3920–3924.
[15] a) T. Jerphagnon, R. Haak, F. Berthiol, A. J. A. Gayet,
V. Ritleng, A. Holuigue, N. Pannetier, M. Pfeffer, A.
Voelklin, L. Lefort, G. Verzijl, C. Tarabiono, D. B. Jans-
sen, A. J. Minnaard, B. L. Feringa, J. G. Vries, Top.
Catal. 2010, 53, 1002–1008; b) N. Pannetier, J.-B. Sor-
tais, J.-T. Issenhuth, L. Barloy, C. Sirlin, A. Holuigue,
L. Lefort, L. Panella, J. G. Vries, M. Pfeffer, Adv.
Synth. Catal. 2011, 353, 2844–2852.
[6] For example, see: a) J. W. Faller, A. R. Lavoie, Org.
Lett. 2001, 3, 3703–3706; b) W. Baratta, M. Ballico, A.
Del Zotto, K. Siega, S. Magnolia, P. Rigo, Chem. Eur. J.
2008, 14, 2557–2563.
[7] For examples of iron-based catalysts, see: a) C. P.
Casey, H. Guan, J. Am. Chem. Soc. 2007, 129, 5816–
Adv. Synth. Catal. 0000, 000, 0 – 0
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