-
2
-
-
2542478906
-
-
b) S. Ranganathan, K. M. Muraleedharan, N. K. Vaish, N. Jayaraman, Tetrahedron 2004, 60, 5273-5308;
-
(2004)
Tetrahedron
, vol.60
, pp. 5273-5308
-
-
Ranganathan, S.1
Muraleedharan, K.M.2
Vaish, N.K.3
Jayaraman, N.4
-
3
-
-
4444307147
-
-
c) A. N. French, S. Bissmire, T. Wirth, Chem. Soc. Rev. 2004, 33, 354-362;
-
(2004)
Chem. Soc. Rev.
, vol.33
, pp. 354-362
-
-
French, A.N.1
Bissmire, S.2
Wirth, T.3
-
4
-
-
69249110928
-
-
d) M. S. Laya, A. K. Banerjee, E. V. Cabrera, Curr. Org. Chem. 2009, 13, 720-730
-
(2009)
Curr. Org. Chem.
, vol.13
, pp. 720-730
-
-
Laya, M.S.1
Banerjee, A.K.2
Cabrera, E.V.3
-
5
-
-
1842638312
-
-
Only two reports of moderately selective enantioselective iodolactonization have appeared to date: a) M. Wang, L. X. Gao, W. P. Mai, A. X. Xia, F. Wang, S. B. Zhang, J. Org. Chem. 2004, 69, 2874-2876;
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2874-2876
-
-
Wang, M.1
Gao, L.X.2
Mai, W.P.3
Xia, A.X.4
Wang, F.5
Zhang, S.B.6
-
6
-
-
69449091001
-
-
b) Z. L. Ning, R. H. Jin, J. Y. Ding, L. X. Gao, Synlett 2009, 2291-2294
-
(2009)
Synlett
, pp. 2291-2294
-
-
Ning, Z.L.1
Jin, R.H.2
Ding, J.Y.3
Gao, L.X.4
-
7
-
-
37049067942
-
-
For examples of reagent-controlled enantioselective iodolactonization see: a) O. Kitagawa, T. Hanano, K. Tanabe, M. Shiro, T. Taguchi, J. Chem. Soc. Chem. Commun. 1992, 1005-1007;
-
(1992)
J. Chem. Soc. Chem. Commun.
, pp. 1005-1007
-
-
Kitagawa, O.1
Hanano, T.2
Tanabe, K.3
Shiro, M.4
Taguchi, T.5
-
9
-
-
0012128041
-
-
c) J. Haas, S. Piguel, T. Wirth, Org. Lett. 2002, 4, 297-300;
-
(2002)
Org. Lett.
, vol.4
, pp. 297-300
-
-
Haas, J.1
Piguel, S.2
Wirth, T.3
-
10
-
-
25444442832
-
-
d) J. Haas, S. Bissmire, T. Wirth, Chem. Eur. J. 2005, 11, 5777-5785;
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 5777-5785
-
-
Haas, J.1
Bissmire, S.2
Wirth, T.3
-
12
-
-
0346365076
-
-
For successful examples of other types of enantioselective halocyclization reactions see: a) S. H. Kang, S. B. Lee, C. M. Park, J. Am. Chem. Soc. 2003, 125, 15748-15749;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 15748-15749
-
-
Kang, S.H.1
Lee, S.B.2
Park, C.M.3
-
13
-
-
33847218271
-
-
b) A. Sakakura, A. Ukai, K. Ishihara, Nature 2007, 445, 900-903;
-
(2007)
Nature
, vol.445
, pp. 900-903
-
-
Sakakura, A.1
Ukai, A.2
Ishihara, K.3
-
14
-
-
77950502403
-
-
c) D. C. Whitehead, R. Yousefi, A. Jaganathan, B. Borhan, J. Am. Chem. Soc. 2010, 132, 3298-3300;
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 3298-3300
-
-
Whitehead, D.C.1
Yousefi, R.2
Jaganathan, A.3
Borhan, B.4
-
15
-
-
77949791576
-
-
d)W. Zhang, S. Q. Zheng, N. Liu, J. B. Werness, I. A. Guzei, W. P. Tang, J. Am. Chem. Soc. 2010, 132, 3664-3665.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 3664-3665
-
-
Zhang, W.1
Zheng, S.Q.2
Liu, N.3
Werness, J.B.4
Guzei, I.A.5
Tang, W.P.6
-
19
-
-
35948942795
-
-
b) I. T. Raheem, P. S. Thiara, E. A. Peterson, E. N. Jacobsen, J. Am. Chem. Soc. 2007, 129, 13404-13405;
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 13404-13405
-
-
Raheem, I.T.1
Thiara, P.S.2
Peterson, E.A.3
Jacobsen, E.N.4
-
22
-
-
70349914539
-
-
Angew. Chem. Int. Ed. 2009, 48, 6328-6331;
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6328-6331
-
-
-
23
-
-
77950805314
-
-
e) R. R. Knowles, S. Lin, E. N. Jacobsen, J. Am. Chem. Soc. 2010, 132, 5030-5032
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 5030-5032
-
-
Knowles, R.R.1
Lin, S.2
Jacobsen, E.N.3
-
25
-
-
77149152524
-
-
b) H. Xu, S. J. Zuend, M. G.Woll, Y. Tao, E. N. Jacobsen, Science 2010, 327, 986-990
-
(2010)
Science
, vol.327
, pp. 986-990
-
-
Xu, H.1
Zuend, S.J.2
Woll, M.G.3
Tao, Y.4
Jacobsen, E.N.5
-
26
-
-
72249110249
-
-
C. K. De, E. G. Klauber, D. Seidel, J. Am. Chem. Soc. 2009, 131, 17060-17061
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17060-17061
-
-
De, C.K.1
Klauber, E.G.2
Seidel, D.3
-
28
-
-
44949230317
-
-
S. E. Reisman, A. G. Doyle, E. N. Jacobsen, J. Am. Chem. Soc. 2008, 130, 7198-7199.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7198-7199
-
-
Reisman, S.E.1
Doyle, A.G.2
Jacobsen, E.N.3
-
29
-
-
77957376619
-
-
Details of the catalyst screen are provided in the Supporting Information
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Details of the catalyst screen are provided in the Supporting Information
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-
-
-
30
-
-
48249126276
-
-
V. K. Chaikovskii, A. A. Funk, V. D. Filiminov, T. V. Petrenko, T. S. Kets, Russ. J. Org. Chem. 2008, 44, 935-938
-
(2008)
Russ. J. Org. Chem.
, vol.44
, pp. 935-938
-
-
Chaikovskii, V.K.1
Funk, A.A.2
Filiminov, V.D.3
Petrenko, T.V.4
Kets, T.S.5
-
31
-
-
77957337833
-
-
For full details of the optimization of the N-iodoimide see the Supporting Information
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For full details of the optimization of the N-iodoimide see the Supporting Information
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-
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77957359500
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1H NMR spectrum comparable to those observed upon protonation of 1 with strong mineral acids. See Supporting Information for further details
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1H NMR spectrum comparable to those observed upon protonation of 1 with strong mineral acids. See Supporting Information for further details
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33
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77957375508
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DFT calculations were performed using the hybrid GGA functional B3PW91/6-31g(d) with a modified SDD pseudopotential, as described in Ref. [3d]
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DFT calculations were performed using the hybrid GGA functional B3PW91/6-31g(d) with a modified SDD pseudopotential, as described in Ref. [3d]
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-
-
-
34
-
-
0034987510
-
-
M. Date, Y. Tamai, T. Hattori, H. Takayama, Y. Kamikubo, S. Miyano, J. Chem. Soc. Perkin Trans. 1 2001, 2001, 645-653
-
(2001)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 645-653
-
-
Date, M.1
Tamai, Y.2
Hattori, T.3
Takayama, H.4
Kamikubo, Y.5
Miyano, S.6
-
35
-
-
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-
-
CCDC 781487 (3g) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif
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CCDC 781487 (3g) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www. ccdc.cam.ac.uk/data-request/cif
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