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Organic & Biomolecular Chemistry
Page 4 of 4
COMMUNICATION
Journal Name
Lett., 2016, 18, 956; (e) A. Ponce, I. Alonso, J. Adrio and J. C.
Carretero, Chem. Eur. J., 2016, 22, 4952; (f) M. Ma, Y. Zhu, Q.
Sun, X. Li, J. Su, L. Zhao, Y. Zhao, S. Qiu, W. Yan, K. Wang, and
R. Wang, Chem. Commun., 2015, 51, 8789; (g) Q. Sun, X. Li, J.
Su, L. Zhao, M. Ma, Y. Zhu, Y. Zhao, R. Zhu, W. Yan, K. Wang,
and R. Wang, Adv. Synth. Catal., 2015, 357, 3187; (h) M. T.
Corbett, Q. Xu and J. S. Johnson, Org. Lett., 2014, 16, 2362; (i)
G. Huang, Z. Yin and X. Zhang, Chem. Eur. J., 2013, 19, 11992;
(j) H. Kawai, S. Okusu, Z. Yuan, E. Tokunaga, A. Yamano, M.
Shiro and N. Shibata, Angew. Chem. Int. Ed., 2013, 52, 2221;
(k) H. Kawai, Z. Yuan, T. Kitayama, E. Tokunaga and N.
Shibata, Angew. Chem. Int. Ed., 2013, 52, 5575; (l) Y. Su, J.-B.
Ling, S. Zhang and P.-F. Xu, J. Org. Chem., 2013, 78, 11053;
(m) H. Kawai, S. Okusu, E. Tokunaga, H. Sato, M. Shiro and N.
Shibata, Angew. Chem. Int. Ed., 2012, 51, 4959; (n) H. Kawai,
T. Kitayama, E. Tokunaga, T. Matsumoto, H. Sato, M. Shiro
and N. Shibata, Chem. Commun., 2012, 48, 4067; (o) H.
Kawai, Y. Sugita, E. Tokunaga, H. Sato, M. Shiro and N.
Shibata, Chem. Commun., 2012, 48, 3632; (p) Q.-H. Li, Z.-Y.
Catal., 2013, 355, 1989; (f) Z. X. Jia, DYO. IC: 1.0L.1u0o3,9/YC.7OWBa0n10g1,3LC.
Chen, P. F. Xu and B. Wang, Chem. Eur. J. , 2012, 18, 12958;
(g) L.-Q. Lu, J.-R. Chen and W.-J. Xiao, Acc. Chem. Res., 2012,
45, 1278; (h) C. Liu, X. Zhang, R. Wang and W. Wang, Org.
Lett., 2010, 12, 4948; (i) J. Wang, H. Xie, H. Li, L. Zu and W.
Wang, Angew. Chem. Int. Ed., 2008, 47, 4177; (j) R. Dodda, J.
J. Goldman, T. Mandel, C.-G. Zhao, G. A. Broker and E. R. T.
Tiekink, Adv. Synth. Catal., 2008, 350, 537; (k) L. Zu, J. Wang,
H. Li, H. Xie, W. Jiang and W. Wang, J. Am. Chem. Soc., 2007,
129, 1036;
7
For selected asymmetric reactions concerning β-CF3
nitroalkene, see: (a) X. Hou, H. Ma, Z. Zhang, L. Xie, Z. Qin
and B. Fu, Chem. Commun., 2016, 52, 1470; (b) Y. Zhao, X.-J.
Wang, Y. Lin, C.-X. Cai and J.-T. Liu, Tetrahedron, 2014, 70
2523; (c) J.-H. Lin and J.-C. Xiao, Eur. J. Org. Chem., 2011, 11
,
,
4536; (d) M. P. Lalonde, Y. Chen and E. N. Jacobsen, Angew.
Chem. Int. Ed., 2006, 45, 636.
Xue, H.-Y. Tao and C.-J. Wang, Tetrahedron Lett, 2012, 53
,
8
9
For selected reviews on organocatalysis, see: (a) A. G. Doyle
and E. N. Jacobsen, Chem. Rev., 2007, 107, 5713; (b) P. I.
Dalko and L. Moisan, Angew. Chem., Int. Ed., 2004, 43, 5138.
We also investigated N-Ac, N-Boc, N-Bz and N-Cbz protected
substrates, but no corresponding products were found under
the same reaction conditions.
3650; (q) Q.-H. Li, M.-C. Tong, J. Li, H.-Y. Tao and C.-J. Wang,
Chem. Commun., 2011, 47, 11110; (r) K. Matoba, H. Kawai, T.
Furukawa, A. Kusuda, E. Tokunaga, S. Nakamura, M. Shiro
and N. Shibata, Angew. Chem. Int. Ed., 2010, 49, 5762.
For selected synthesis of CF3-containing six-membered
heterocycles, see: (a) Y. Zhu, Z. Dong, X. Cheng, X. Zhong, X. 10 CCDC 1535828 contains the supplementary crystallographic
Liu, L. Lin, Z. Shen, P. Yang, Y. Li, H. Wang, W. Yan, K. Wang
and R. Wang, Org. Lett., 2016, 18, 3546; (b) Y. Zhu, X. Li, Q.
Chen, J. Su, F. Jia, S. Qiu, M. Ma, Q. Sun, W. Yan, K. Wang and
R. Wang, Org. Lett., 2015, 17, 3826; (c) Z.-P. Chen, S.-B. Hu, J.
Zhou and Y.-G. Zhou, ACS Catal., 2015, 5, 6086; (d) G. L. 11 CCDC 1535827 contains the supplementary crystallographic
Grunewald, J. Lu, K. R. Criscione and C. O. Okoro, Bioorg.
Med. Chem. Lett., 2005, 15, 5319.
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data for the compound 3oa reported in this paper. These
data can be obtained free of charge from The Cambridge
Crystallographic
Data
Centre
via
data for the compound 3ta reported in this paper. These
data can be obtained free of charge from The Cambridge
For selected reviews, see: (a) Y. Zhou, J. Wang, Z. Gu, S.
Wang, W. Zhu, J. L. Aceꢀa, V. A. Soloshonok, K. Izawa and H.
Liu, Chem. Rev., 2016, 116, 422; (b) X. Yang, T. Wu, R. J.
Phipps and F. D. Toste, Chem. Rev., 2015, 115, 826; (c) J.
Wang, M. Sánchez-Roselló, J. L. Aceña, C. D. del Pozo, A. E.
Sorochinsky, S. Fustero, V. A. Soloshonok and H. Liu, Chem.
Rev., 2014, 114, 2432; (d) W. Zhu, J. Wang, S. Wang, Z. Gu, J.
L. Aceña, K. Izawa, H. Liu and V. A. Soloshonok, J. Fluorine
Chem., 2014, 167, 37; (e) Y. Zheng and J.-A. Ma, Adv. Synth.
Catal., 2010, 352, 2745; (f) R. Smits, C. D. Cadicamo, K.
Burger and B. Koksch, Chem. Soc. Rev., 2008, 37, 1727; (g) S.
Purser, P. R. Moore, S. Swallow and V. Gouverneur, Chem.
Soc. Rev., 2008, 37, 320; (h) J.-A. Ma and D. Cahard, Chem.
Rev., 2008, 108, PR1-PR43; (i) M. Sani, A. Volonterio and M.
Crystallographic
Data
Centre
via
Zanda, Chem. Med-Chem., 2007, 2, 1693.
5
For selected reviews, see: (a) V. Sridharan, P. A. Suryavanshi
and J. C. Menéndez, Chem. Rev., 2011, 111, 7157. For
selected examples, see: (b) R. J. Pagliero, S. Lusvarghi, A. B.
Pierini, R. Brun and M. R. Mazzieri, Bioorganic Med. Chem.,
2010, 18, 142; (c) J. Liu, Y. Wang, Y. Sun, D. Marshall, S. Miao,
G. Tonn, P. Anders, J. Tocker, H. L. Tang and J. Medina,
Bioorganic Med. Chem. Lett., 2009, 19, 6840; (d) D. Enders, C.
Wang and J. X. Liebich, Chem. Eur. J., 2009, 15, 11058; (e) I.
Jacquemond-Collet, S. Benoit-Vical, V. Mustofa, A. alentin, E.
Stanislas, M. Mallié and I. Fourasté, Planta Med., 2002, 68
,
68; (f) I. Jacquemond-Collet, S. Hannedouche, N. Fabre, I.
Fourasté and C. Moulis, Phytochemistry, 1999, 51, 1167; (g) P.
J. Houghton, T. Z. Woldemariam, Y. Watanabe and M. Yates,
Planta Med., 1999, 65, 250; (h) A. R. Katritzky, S. Rachwal
and B. Rachwal, Tetrahedron, 1996, 52, 15031.
For selected cascade reactions, see: (a) P. Chauhan, S.
Mahajan, U. Kaya, D. Hack and D. Enders, Adv. Synth. Catal.,
2015, 357, 253; (b) Z.-X. Jia, Y.-C. Luo, X.-N. Cheng, P.-F. Xu
and Y.-C. Gu, J. Org. Chem., 2013, 78, 6488; (c) W. Yang, Y.
Yang and D.-M. Du, Org. Lett., 2013, 15, 1190; (d) W. Yang, H.
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4 | J. Name., 2012, 00, 1-3
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