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COMMUNICATION
Journal Name
data for compound (R)-4g. This data caDnObI:e1o0.b10ta3i9n/eCd6CfCre0e12o7f3F
charge from The Cambridge Crystallographic Data Centre via
We thank the National Natural Science Foundation of China, the
National Basic Research Program of China (2012CB821600), the
“111” project (B06005) of the Ministry of Education of China,
and the National Program for Support of Top-notch Young
Professionals for financial support.
11 H. Ohta, N. Kobayashi and K. Ozaki, J. Org. Chem., 1989, 54
,
1802.
Notes and references
1
For reviews, see: (a) N. Ono, The Nitro Group in Organic
Synthesis; Wiley-VCH: New York, 2001; (b) R. Ballini and M.
Petrini, Tetrahedron, 2004, 60, 1017.
2
For selected examples of conjugate addition, see: (a) A.
Alexakis, C. Benhaim, S. Rosset and M. Humam, J. Am. Chem.
Soc., 2002, 124, 5262; (b) T. Ishii, S. Fujioka, Y. Sekiguchi and
H. Kotsuki, J. Am. Chem. Soc., 2004, 126, 9558; (c) J. Wu, D. M.
Mampreian and A. H. Hoveyda, J. Am. Chem. Soc., 2005, 127
,
4584; (d) Y. Zhu, J. P. Malerich and V. H. Rawal, Angew. Chem.
Int. Ed., 2010, 49, 153; (e) Z.-Q. Wang, C.-G. Feng, S.-S. Zhang,
M.-H. Xu and G.-Q. Lin, Angew. Chem. Int. Ed., 2010, 49, 5780;
(f) C. Curti, G. Rassu, V. Zambrano, L. Pinna, G. Pelosi, A.
Sartori, L. Battistini, F. Zanardi and G. Casiraghi, Angew. Chem.
Int. Ed.; 2012, 51, 6200; for selected examples of transfer
hydrogenation, see: (g) C. Czekelius and E. M. Carreira, Angew.
Chem. Int. Ed.; 2003, 42, 4793; (h) N. J. A. Martin, L. Ozores
and B. List, J. Am. Chem. Soc., 2007, 129, 8976; (i) L.-A. Chen,
W. Xu, B. Huang, J. Ma, L. Wang, J. Xi, K. Harms, L. Gong and E.
Meggers, J. Am. Chem. Soc., 2013, 135, 10598.
3
For reviews on asymmetric hydrogenation, see: (a) W. Tang
and X. Zhang, Chem. Rev., 2003, 103, 3029; (b) J.-H. Xie, S.-F.
Zhu and Q.-L. Zhou, Chem. Rev., 2011, 111, 1713.
4
5
S. Li, K. Huang, B. Cao, J. Zhang, W. Wu and X. Zhang, Angew.
Chem. Int. Ed., 2012, 51, 8573.
(a) S. Li, K. Huang, J. Zhang, W. Wu and X. Zhang, Chem. Eur.
J., 2013, 19, 10840; (b) Q. Zhao, S. Li, K. Huang, R. Wang and
X. Zhang, Org. Lett., 2013, 15, 4014; (c) M. Liu, D. Kong, M. Li,
G. Zi and G. Hou, Adv. Synth. Catal., 2015, 357, 3875; for
asymmetric hydrogenation of β-amino or β-ester substituted
nitroalkenes: (d) M. Zhou, D. Dong, B. Zhu, H. Geng, Y. Wang
and X. Zhang, Org. Lett., 2013, 15, 5524; (e) Q. Yan, M. Liu, D.
Kong, G. Zi and G. Hou, Chem. Commun., 2014, 50, 12870; (f)
S. Li, T. Xiao, D. Li and X. Zhang, Org. Lett., 2015, 17, 3782; (g)
P. Li, M. Zhou, Q. Zhao, W. Wu, X. Hu, X.-Q. Dong and X. Zhang,
Org. Lett., 2016, 18, 40; for asymmetric hydrogenation of α,β-
disubstituted nitroalkenes: (h) S. Li, K. Huang and X. Zhang,
Chem. Commun., 2014, 50, 8878.
6
7
S. Song, S.-F. Zhu, Y.-B. Yu and Q.-L. Zhou, Angew. Chem. Int.
Ed., 2013, 52, 1556 and references therein.
(a) Y.-J. Jang, W.-W. Lin, Y.-K. Shih, J.-T. Liu, M.-H. Hwang and
C.-F. Yao, Tetrahedron, 2003, 59, 4979; (b) A. Fryszkowska, K.
Fisher, J. M. Gardiner and G. M. Stephens, J. Org. Chem., 2008,
73, 4295; (c) S. Maity, S. Manna, S. Rana, T. Naveen, A. Mallick
and D. Maiti, J. Am. Chem. Soc., 2013, 135, 3355.
8
9
(a) S.-F. Zhu, Y.-B. Yu, S. Li, L.-X. Wang and Q.-L. Zhou, Angew.
Chem. Int. Ed., 2012, 51, 8872; for reviews on chiral spiro
ligands, see: (b) S.-F. Zhu and Q.-L. Zhou, in Privileged Chiral
Ligands and Catalysts; Zhou, Q.-L. Ed.; Wiley-VCH: Weinheim,
2011; chapter 4, p 137; (c) J.-H. Xie and Q.-L. Zhou, Acc. Chem.
Res. 2008, 41, 581; (d) K. Ding, Z. Han and Z. Wang, Chem.
Asian J. 2009, 4, 32; (e) J.-H. Xie and Q.-L. Zhou, Acta Chim.
Sinica, 2014, 72, 778.
For the synthesis of compound 5, see: (a) S.-F. Zhu, J.-B. Xie,
Y.-Z. Zhang, S. Li and Q.-L. Zhou, J. Am. Chem. Soc., 2006, 128
,
12886; for the addition of organometallic reagents to nitriles,
see: (b) E. Ciganek, J. Org. Chem., 1992, 57, 4521; (c) O.
Tomashenko, V. Sokolov, A. Tomashevskiy and A. Meijere,
Synlett, 2007, 652.
4 | J. Name., 2012, 00, 1-3
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