-
1
-
-
84991836410
-
-
For selected reviews, see
-
For selected reviews, see
-
-
-
-
3
-
-
77954271846
-
-
F. Zhou, Y.-L. Liu, J. Zhou, Adv. Synth. Catal. 2010, 352, 1381;
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1381
-
-
Zhou, F.1
Liu, Y.-L.2
Zhou, J.3
-
5
-
-
84991871775
-
-
For reviews, see
-
For reviews, see
-
-
-
-
8
-
-
60749118899
-
-
Angew. Chem. 2007, 119, 8902;
-
(2007)
Angew. Chem.
, vol.119
, pp. 8902
-
-
-
9
-
-
84898873012
-
-
R. Narayan, M. Potowski, Z.-J. Jia, A. P. Antonchick, H. Waldmann, Acc. Chem. Res. 2014, 47, 1296.
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 1296
-
-
Narayan, R.1
Potowski, M.2
Jia, Z.-J.3
Antonchick, A.P.4
Waldmann, H.5
-
10
-
-
84991889155
-
-
Selected examples on bioactivities and synthetic applications, see
-
Selected examples on bioactivities and synthetic applications, see
-
-
-
-
11
-
-
22944473048
-
-
K. J. Ding, Y. Lu, Z. Nikolovska-Coleska, J. Am. Chem. Soc. 2005, 127, 10130;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10130
-
-
Ding, K.J.1
Lu, Y.2
Nikolovska-Coleska, Z.3
-
12
-
-
33745154819
-
-
K. J. Ding, Y. Lu, Z. Nikolovska-Coleska, J. Med. Chem. 2006, 49, 3432;
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3432
-
-
Ding, K.J.1
Lu, Y.2
Nikolovska-Coleska, Z.3
-
13
-
-
41649102468
-
-
S. Shangary, D. Qin, D. McEachern, Proc. Natl. Acad. Sci. USA 2008, 105, 3933;
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 3933
-
-
Shangary, S.1
Qin, D.2
McEachern, D.3
-
14
-
-
34247851027
-
-
C. Li, C. Chan, A. C. Heimann, S. J. Danishefsky, Angew. Chem. Int. Ed. 2007, 46, 1444;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1444
-
-
Li, C.1
Chan, C.2
Heimann, A.C.3
Danishefsky, S.J.4
-
15
-
-
84991864003
-
-
Angew. Chem. 2007, 119, 1466.
-
(2007)
Angew. Chem.
, vol.119
, pp. 1466
-
-
-
16
-
-
84991846756
-
-
Selected examples with organocatalysts, see
-
Selected examples with organocatalysts, see
-
-
-
-
17
-
-
70349742473
-
-
X.-H. Chen, Q. Wei, S.-W. Luo, H. Xiao, L.-Z. Gong, J. Am. Chem. Soc. 2009, 131, 13819;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 13819
-
-
Chen, X.-H.1
Wei, Q.2
Luo, S.-W.3
Xiao, H.4
Gong, L.-Z.5
-
18
-
-
80052833054
-
-
Y. Cao, X. Jiang, L. Liu, F. Shen, F. Zhang, R. Wang, Angew. Chem. Int. Ed. 2011, 50, 9124;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 9124
-
-
Cao, Y.1
Jiang, X.2
Liu, L.3
Shen, F.4
Zhang, F.5
Wang, R.6
-
19
-
-
84555211692
-
-
Angew. Chem. 2011, 123, 9290;
-
(2011)
Angew. Chem.
, vol.123
, pp. 9290
-
-
-
20
-
-
84555191597
-
-
B. Tan, X. Zeng, W. W. Y. Leong, Z. Shi, C. F. Barbas III, G. Zhong, Chem. Eur. J. 2012, 18, 63;
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 63
-
-
Tan, B.1
Zeng, X.2
Leong, W.W.Y.3
Shi, Z.4
Barbas, C.F.5
Zhong, G.6
-
21
-
-
84876530424
-
-
For related works, see
-
L. Wang, X.-M. Shi, W.-P. Dong, L.-P. Zhu, R. Wang, Chem. Commun. 2013, 49, 3458. For related works, see
-
(2013)
Chem. Commun.
, vol.49
, pp. 3458
-
-
Wang, L.1
Shi, X.-M.2
Dong, W.-P.3
Zhu, L.-P.4
Wang, R.5
-
22
-
-
84861544403
-
-
F. Shi, Z.-L. Tao, S.-W. Luo, S.-J. Tu, L.-Z. Gong, Chem. Eur. J. 2012, 18, 6885;
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 6885
-
-
Shi, F.1
Tao, Z.-L.2
Luo, S.-W.3
Tu, S.-J.4
Gong, L.-Z.5
-
23
-
-
84860376945
-
-
L.-L. Wang, J.-F. Bai, L. Peng, L.-W. Qi, L.-N. Jia, Y.-L. Guo, X.-Y. Luo, X.-Y. Xu, L.-X. Wang, Chem. Commun. 2012, 48, 5175;
-
(2012)
Chem. Commun.
, vol.48
, pp. 5175
-
-
Wang, L.-L.1
Bai, J.-F.2
Peng, L.3
Qi, L.-W.4
Jia, L.-N.5
Guo, Y.-L.6
Luo, X.-Y.7
Xu, X.-Y.8
Wang, L.-X.9
-
24
-
-
84872454361
-
-
Y.-M. Cao, F.-F. Shen, F.-T. Zhang, R. Wang, Chem. Eur. J. 2013, 19, 1184;
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 1184
-
-
Cao, Y.-M.1
Shen, F.-F.2
Zhang, F.-T.3
Wang, R.4
-
25
-
-
84906845813
-
-
J.-A. Xiao, Q. Liu, J.-W. Ren, J. Liu, R. G. Carter, X.-Q. Chen, H. Yang, Eur. J. Org. Chem. 2014, 5700.
-
(2014)
Eur. J. Org. Chem.
, pp. 5700
-
-
Xiao, J.-A.1
Liu, Q.2
Ren, J.-W.3
Liu, J.4
Carter, R.G.5
Chen, X.-Q.6
Yang, H.7
-
26
-
-
84991868135
-
-
Selected examples with chiral Lewis acids, see
-
Selected examples with chiral Lewis acids, see
-
-
-
-
27
-
-
77956042533
-
-
P. A. Antonchick, C. Gerfing-Reimers, M. Catarinella, M. Schürmann, H. Preut, S. Ziegler, D. Rauh, H. Waldmann, Nat. Chem. 2010, 2, 735;
-
(2010)
Nat. Chem.
, vol.2
, pp. 735
-
-
Antonchick, P.A.1
Gerfing-Reimers, C.2
Catarinella, M.3
Schürmann, M.4
Preut, H.5
Ziegler, S.6
Rauh, D.7
Waldmann, H.8
-
28
-
-
82255191940
-
-
P. A. Antonchick, H. Schuster, H. Bruss, M. Schürmann, H. Preut, D. Rauh, H. Waldmann, Tetrahedron 2011, 67, 10195;
-
(2011)
Tetrahedron
, vol.67
, pp. 10195
-
-
Antonchick, P.A.1
Schuster, H.2
Bruss, H.3
Schürmann, M.4
Preut, H.5
Rauh, D.6
Waldmann, H.7
-
29
-
-
79952182033
-
-
T.-L. Liu, Z.-Y. Xue, H.-Y. Tao, C.-J. Wang, Org. Biomol. Chem. 2011, 9, 1980;
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 1980
-
-
Liu, T.-L.1
Xue, Z.-Y.2
Tao, H.-Y.3
Wang, C.-J.4
-
31
-
-
84921532069
-
-
T. Arai, H. Ogawa, A. Awata, M. Sato, M. Watabe, M. Yamanaka, Angew. Chem. Int. Ed. 2015, 54, 1595;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 1595
-
-
Arai, T.1
Ogawa, H.2
Awata, A.3
Sato, M.4
Watabe, M.5
Yamanaka, M.6
-
32
-
-
84969676562
-
-
For a related work, see
-
Angew. Chem. 2015, 127, 1615. For a related work, see
-
(2015)
Angew. Chem.
, vol.127
, pp. 1615
-
-
-
33
-
-
84894095359
-
-
F. Salahi, M. J. Taghizadeh, H. Arvinnezhad, M. Moemeni, K. Jadidi, B. Notash, Tetrahedron Lett. 2014, 55, 1515.
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 1515
-
-
Salahi, F.1
Taghizadeh, M.J.2
Arvinnezhad, H.3
Moemeni, M.4
Jadidi, K.5
Notash, B.6
-
34
-
-
84991904256
-
-
For selected reviews, see
-
For selected reviews, see
-
-
-
-
37
-
-
84990192870
-
-
Angew. Chem. 2008, 120, 52;
-
(2008)
Angew. Chem.
, vol.120
, pp. 52
-
-
-
38
-
-
84880296641
-
-
W. R. J. D. Galloway, A. Isidro-Llobet, D. R. Spring, Nat. Commun. 2010, 1, 80;
-
(2010)
Nat. Commun.
, vol.1
, pp. 80
-
-
Galloway, W.R.J.D.1
Isidro-Llobet, A.2
Spring, D.R.3
-
39
-
-
84862008385
-
-
C. J. O′ Connor, H. S. G. Beckmannw, D. R. Spring, Chem. Soc. Rev. 2012, 41, 4444.
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 4444
-
-
O'Connor, C.A.1
Beckmannw, H.S.G.2
Spring, D.R.3
-
40
-
-
84991894756
-
-
For reviews, see
-
For reviews, see
-
-
-
-
42
-
-
84991908577
-
-
Ed.: A. K. Yudin, Wiley-VCH, Weinheim, Chapter
-
H. Ohno, in Aziridines and Epoxides in Asymmetric Synthesis (Ed.:, A. K. Yudin,), Wiley-VCH, Weinheim, 2006, Chapter 2;
-
(2006)
Aziridines and Epoxides in Asymmetric Synthesis
, vol.2
-
-
Ohno, H.1
-
44
-
-
84991908342
-
-
in (Eds: E. Schaumann, D. Enders), Georg Thieme, Stuttgart
-
J. B. Sweeney, in Science of Synthesis, Vol. 40a (Eds:, E. Schaumann, D. Enders,), Georg Thieme, Stuttgart, 2009, pp. 643;
-
(2009)
Science of Synthesis, Vol. 40a
, pp. 643
-
-
Sweeney, J.B.1
-
46
-
-
84991867483
-
-
Selected work, see
-
Selected work, see
-
-
-
-
47
-
-
0001219079
-
-
T. Ibuka, N. Mimura, H. Aoyama, M. Akaji, H. Ohno, Y. Miwa, T. Taga, K. Nakai, H. Tamamura, N. Fujii, J. Org. Chem. 1997, 62, 999;
-
(1997)
J. Org. Chem.
, vol.62
, pp. 999
-
-
Ibuka, T.1
Mimura, N.2
Aoyama, H.3
Akaji, M.4
Ohno, H.5
Miwa, Y.6
Taga, T.7
Nakai, K.8
Tamamura, H.9
Fujii, N.10
-
48
-
-
0037162742
-
-
K. Aoyagi, H. Nakamura, Y. Yamamoto, J. Org. Chem. 2002, 67, 5977;
-
(2002)
J. Org. Chem.
, vol.67
, pp. 5977
-
-
Aoyagi, K.1
Nakamura, H.2
Yamamoto, Y.3
-
49
-
-
23744509485
-
-
J. G. Knight, K. Tchabanenko, P. A. Stoker, S. J. Harwood, Tetrahedron Lett. 2005, 46, 6261;
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 6261
-
-
Knight, J.G.1
Tchabanenko, K.2
Stoker, P.A.3
Harwood, S.J.4
-
50
-
-
40649092510
-
-
J. G. Knight, P. A. Stoker, K. Tchabanenko, S. J. Harwood, K. W. Lawrie, Tetrahedron 2008, 64, 3744;
-
(2008)
Tetrahedron
, vol.64
, pp. 3744
-
-
Knight, J.G.1
Stoker, P.A.2
Tchabanenko, K.3
Harwood, S.J.4
Lawrie, K.W.5
-
51
-
-
74949090496
-
-
S. Baktharaman, N. Afagh, A. Vandersteen, A. K. Yudin, Org. Lett. 2010, 12, 240;
-
(2010)
Org. Lett.
, vol.12
, pp. 240
-
-
Baktharaman, S.1
Afagh, N.2
Vandersteen, A.3
Yudin, A.K.4
-
52
-
-
79959748114
-
-
M. A. Lowe, M. Ostovar, S. Ferrini, C. C. Chen, P. G. Lawrence, F. Fontana, A. A. Calabrese, V. K. Aggarwal, Angew. Chem. Int. Ed. 2011, 50, 6370;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 6370
-
-
Lowe, M.A.1
Ostovar, M.2
Ferrini, S.3
Chen, C.C.4
Lawrence, P.G.5
Fontana, F.6
Calabrese, A.A.7
Aggarwal, V.K.8
-
53
-
-
84864251469
-
-
Angew. Chem. 2011, 123, 6494;
-
(2011)
Angew. Chem.
, vol.123
, pp. 6494
-
-
-
54
-
-
84882778073
-
-
G. Arena, C. C. Chen, D. Leonori, V. K. Aggarwal, Org. Lett. 2013, 15, 4250.
-
(2013)
Org. Lett.
, vol.15
, pp. 4250
-
-
Arena, G.1
Chen, C.C.2
Leonori, D.3
Aggarwal, V.K.4
-
55
-
-
84921476976
-
-
C.-F. Xu, B.-H. Zheng, J.-J. Suo, C.-H. Ding, X.-L. Hou, Angew. Chem. Int. Ed. 2015, 54, 1604;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 1604
-
-
Xu, C.-F.1
Zheng, B.-H.2
Suo, J.-J.3
Ding, C.-H.4
Hou, X.-L.5
-
56
-
-
84983553167
-
-
For a related reaction of 5-vinyloxazolidinones, see
-
Angew. Chem. 2015, 127, 1624. For a related reaction of 5-vinyloxazolidinones, see
-
(2015)
Angew. Chem.
, vol.127
, pp. 1624
-
-
-
57
-
-
84890931766
-
-
K. Ohmatsu, N. Imagawa, T. Ooi, Nat. Chem. 2013, 6, 47.
-
(2013)
Nat. Chem.
, vol.6
, pp. 47
-
-
Ohmatsu, K.1
Imagawa, N.2
Ooi, T.3
-
58
-
-
84991893219
-
-
For our work on asymmetric heterocycle synthesis, see
-
For our work on asymmetric heterocycle synthesis, see
-
-
-
-
59
-
-
84865343822
-
-
L.-Q. Lu, J.-R. Chen, W.-J. Xiao, Acc. Chem. Res. 2012, 45, 1278;
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 1278
-
-
Lu, L.-Q.1
Chen, J.-R.2
Xiao, W.-J.3
-
60
-
-
84874904079
-
-
H.-G. Cheng, L.-Q. Lu, T. Wang, Q.-Q. Yang, X.-P. Liu, Y. Li, Q.-H. Deng, J.-R. Chen, W.-J. Xiao, Angew. Chem. Int. Ed. 2013, 52, 3250;
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 3250
-
-
Cheng, H.-G.1
Lu, L.-Q.2
Wang, T.3
Yang, Q.-Q.4
Liu, X.-P.5
Li, Y.6
Deng, Q.-H.7
Chen, J.-R.8
Xiao, W.-J.9
-
61
-
-
84956950296
-
-
Angew. Chem. 2013, 125, 3332;
-
(2013)
Angew. Chem.
, vol.125
, pp. 3332
-
-
-
62
-
-
84923239740
-
-
T.-R. Li, F. Tan, L.-Q. Lu, Y. Wei, Y.-N. Wang, Y.-Y. Liu, Q.-Q. Yang, J.-R. Chen, D.-Q. Shi, W.-J. Xiao, Nat. Commun. 2014, 5, 5500;
-
(2014)
Nat. Commun.
, vol.5
, pp. 5500
-
-
Li, T.-R.1
Tan, F.2
Lu, L.-Q.3
Wei, Y.4
Wang, Y.-N.5
Liu, Y.-Y.6
Yang, Q.-Q.7
Chen, J.-R.8
Shi, D.-Q.9
Xiao, W.-J.10
-
63
-
-
84957847718
-
-
Y. Wei, L.-Q. Lu, T.-R. Li, B. Feng, Q. Wang, W.-J. Xiao, H. Alper, Angew. Chem. Int. Ed. 2016, 55, 2200;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 2200
-
-
Wei, Y.1
Lu, L.-Q.2
Li, T.-R.3
Feng, B.4
Wang, Q.5
Xiao, W.-J.6
Alper, H.7
-
64
-
-
84990224792
-
-
Angew. Chem. 2016, 128, 2240.
-
(2016)
Angew. Chem.
, vol.128
, pp. 2240
-
-
-
65
-
-
84991875955
-
-
For selected examples on the construction of multiple continuous stereocentres through Pd-catalyzed AAA reactions, see
-
For selected examples on the construction of multiple continuous stereocentres through Pd-catalyzed AAA reactions, see
-
-
-
-
66
-
-
85027951353
-
-
A. Khan, L. Yang, J. Xu, L. Y. Jin, Y. J. Zhang, Angew. Chem. Int. Ed. 2014, 53, 11257;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 11257
-
-
Khan, A.1
Yang, L.2
Xu, J.3
Jin, L.Y.4
Zhang, Y.J.5
-
67
-
-
84920407616
-
-
Angew. Chem. 2014, 126, 11439;
-
(2014)
Angew. Chem.
, vol.126
, pp. 11439
-
-
-
68
-
-
84954407338
-
-
C.-X. Zhuo, Y. Zhou, Q. Cheng, L. Huang, S.-L. You, Angew. Chem. Int. Ed. 2015, 54, 14146;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 14146
-
-
Zhuo, C.-X.1
Zhou, Y.2
Cheng, Q.3
Huang, L.4
You, S.-L.5
-
69
-
-
84977947629
-
-
ref. 9b and 10e.
-
Angew. Chem. 2015, 127, 14352, ref. 9b and 10e.
-
(2015)
Angew. Chem.
, vol.127
, pp. 14352
-
-
-
70
-
-
84991838528
-
-
For reviews, see
-
For reviews, see
-
-
-
-
72
-
-
78650403767
-
-
Angew. Chem. 2010, 122, 2538;
-
(2010)
Angew. Chem.
, vol.122
, pp. 2538
-
-
-
73
-
-
84957841090
-
-
in (Eds.: P. C. J. Kamer, P. W. N. M. van Leeuwen), Wiley, Chichester, p. . For selected work, see
-
L. Lefort, J. G. de Vries, in Phosphorus (III) Ligands in Homogeneous Catalysis: Design and Synthesis, Vol. 3 (Eds.:, P. C. J. Kamer, P. W. N. M. van Leeuwen,), Wiley, Chichester, 2012, p. 271-314. For selected work, see
-
(2012)
Phosphorus (III) Ligands in Homogeneous Catalysis: Design and Synthesis, Vol. 3
, pp. 271-314
-
-
Lefort, L.1
De Vries, J.G.2
-
74
-
-
85052189785
-
-
D. Peña, A. J. Minnaard, J. G. de Vries, B. L. Feringa, J. Am. Chem. Soc. 2000, 122, 11539;
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11539
-
-
Peña, D.1
Minnaard, A.J.2
De Vries, J.G.3
Feringa, B.L.4
-
76
-
-
84863276579
-
-
W.-B. Liu, C. Zheng, C.-X. Zhuo, L.-X. Dai, S.-L. You, J. Am. Chem. Soc. 2012, 134, 4812-4821;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 4812-4821
-
-
Liu, W.-B.1
Zheng, C.2
Zhuo, C.-X.3
Dai, L.-X.4
You, S.-L.5
-
77
-
-
84947869605
-
-
C.-X. Zhuo, Q. Cheng, W.-B. Liu, Q. Zhao, S.-L. You, Angew. Chem. Int. Ed. 2015, 54, 8475;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 8475
-
-
Zhuo, C.-X.1
Cheng, Q.2
Liu, W.-B.3
Zhao, Q.4
You, S.-L.5
-
78
-
-
84954460496
-
-
Angew. Chem. 2015, 127, 8595.
-
(2015)
Angew. Chem.
, vol.127
, pp. 8595
-
-
-
79
-
-
84991887792
-
-
See the Supporting Information for details.
-
See the Supporting Information for details.
-
-
-
-
80
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84991887723
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The absolute configuration of spirooxindole product 3 h was established X-ray single-crystal diffraction analysis. Other products were assumed according to this result. CCDC 1446828 (3 h) contain the supplementary crystallographic data for this paper. These data are provided free of charge by The Cambridge Crystallographic Data Centre
-
The absolute configuration of spirooxindole product 3 h was established X-ray single-crystal diffraction analysis. Other products were assumed according to this result. CCDC 1446828 (3 h) contain the supplementary crystallographic data for this paper. These data are provided free of charge by The Cambridge Crystallographic Data Centre.
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81
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84991914981
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Other vinyl aziridines, such as 2 c or 2 d, were also tested under the optimal conditions with methyleneindolinone 1 d. However, no desired products were observed, with vinyl aziridines decomposed and methyleneindolinone 1 d retained.
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Other vinyl aziridines, such as 2 c or 2 d, were also tested under the optimal conditions with methyleneindolinone 1 d. However, no desired products were observed, with vinyl aziridines decomposed and methyleneindolinone 1 d retained.
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-
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-
82
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84991890100
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For selected reviews
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For selected reviews
-
-
-
-
84
-
-
80053160683
-
-
Eds.: L. Mander, H.-W. Liu), Elsevier, Amsterdam
-
S. E. O′Connor, in Comprehensive Natural Products II, Vol. 1 (Eds.:, L. Mander, H.-W. Liu,), Elsevier, Amsterdam, 2010, p. 977;
-
(2010)
Comprehensive Natural Products II
, vol.1
, pp. 977
-
-
O'Connor, S.E.1
-
85
-
-
79959400316
-
-
D. Zhang, H. Song, Y. Qin, Acc. Chem. Res. 2011, 44, 447;
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 447
-
-
Zhang, D.1
Song, H.2
Qin, Y.3
-
86
-
-
84925432972
-
-
W. Zi, Z. Zuo, D. Ma, Acc. Chem. Res. 2015, 48, 702.
-
(2015)
Acc. Chem. Res.
, vol.48
, pp. 702
-
-
Zi, W.1
Zuo, Z.2
Ma, D.3
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