-
3
-
-
0011779578
-
-
C. Lee in (Ed.:, 2nd ed., Wiley-VCH, Weinheim, pp. 593-650
-
B. M. Trost, C. Lee in Catalytic Asymmetric Synthesis (Ed.:, I. Ojima), 2nd ed., Wiley-VCH, Weinheim, 2000, pp. 593-650.
-
(2000)
Catalytic Asymmetric Synthesis
-
-
Trost, B.M.1
Ojima, I.2
-
4
-
-
53549095407
-
-
T. E. Müller, K. C. Hultzsch, M. Yus, F. Foubelo, M. Tada, Chem. Rev. 2008, 108, 3795.
-
(2008)
Chem. Rev.
, vol.108
, pp. 3795
-
-
Müller, T.E.1
Hultzsch, K.C.2
Yus, M.3
Foubelo, F.4
Tada, M.5
-
6
-
-
79954589506
-
-
Recent reports on Tsuji-Trost-type allylic amination
-
Recent reports on Tsuji-Trost-type allylic amination
-
-
-
-
9
-
-
39349099756
-
-
L. Banfi, A. Basso, V. Cerulli, G. Guanti, R. Rava, J. Org. Chem. 2008, 73, 1608-1611.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 1608-1611
-
-
Banfi, L.1
Basso, A.2
Cerulli, V.3
Guanti, G.4
Rava, R.5
-
10
-
-
79954612090
-
-
Recent review on the Tsuji-Trost-type reaction of allylic alcohols
-
Recent review on the Tsuji-Trost-type reaction of allylic alcohols
-
-
-
-
11
-
-
16244407390
-
-
J. Muzart, Tetrahedron 2005, 61, 4179-4212.
-
(2005)
Tetrahedron
, vol.61
, pp. 4179-4212
-
-
Muzart, J.1
-
13
-
-
79954586741
-
-
Recent reports on the direct allylic amination of allylic alcohols
-
Recent reports on the direct allylic amination of allylic alcohols
-
-
-
-
14
-
-
8744239436
-
-
H. Kinoshita, H. Shinokubo, K. Oshima, Org. Lett. 2004, 6, 4085-4088.
-
(2004)
Org. Lett.
, vol.6
, pp. 4085-4088
-
-
Kinoshita, H.1
Shinokubo, H.2
Oshima, K.3
-
15
-
-
0037239632
-
-
M. Kimura, M. Futamata, K. Shibata, Y. Tamaru, Chem. Commun. 2003, 234-235.
-
(2003)
Chem. Commun.
, pp. 234-235
-
-
Kimura, M.1
Futamata, M.2
Shibata, K.3
Tamaru, Y.4
-
16
-
-
0037130740
-
-
F. Ozawa, H. Okamoto, S. Kawagishi, S. Yamamoto, T. Minami, M. Yoshifuji, J. Am. Chem. Soc. 2002, 124, 10968-10969.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10968-10969
-
-
Ozawa, F.1
Okamoto, H.2
Kawagishi, S.3
Yamamoto, S.4
Minami, T.5
Yoshifuji, M.6
-
17
-
-
33846451020
-
-
Angew. Chem. Int. Ed. 2007, 46, 409 - 413
-
H. Qin, N. Yamagiwa, S. Matsunaga, M. Shibasaki, Angew. Chem. 2007, 119, 413; Angew. Chem. Int. Ed. 2007, 46, 409-413.
-
(2007)
Angew. Chem.
, vol.119
, pp. 413
-
-
Qin, H.1
Yamagiwa, N.2
Matsunaga, S.3
Shibasaki, M.4
-
18
-
-
77957197373
-
-
H. Yamamoto, E. Ho, K. Namba, H. Imagawa, M. Nishizawa, Chem. Eur. J. 2010, 16, 11271-11274.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 11271-11274
-
-
Yamamoto, H.1
Ho, E.2
Namba, K.3
Imagawa, H.4
Nishizawa, M.5
-
19
-
-
48249129155
-
-
K. Namba, Y. Nakagawa, H. Yamamoto, H. Imagawa, M. Nishizawa, Synlett 2008, 1719-1723.
-
(2008)
Synlett
, pp. 1719-1723
-
-
Namba, K.1
Nakagawa, Y.2
Yamamoto, H.3
Imagawa, H.4
Nishizawa, M.5
-
20
-
-
79954618589
-
-
H. Yamamoto, E. Ho, I. Sasaki, M. Mitsutake, Y. Takagi, H. Imagawa, M. Nishizawa, unpublished results (cf. Supporting Information)
-
H. Yamamoto, E. Ho, I. Sasaki, M. Mitsutake, Y. Takagi, H. Imagawa, M. Nishizawa, unpublished results (cf. Supporting Information).
-
-
-
-
21
-
-
75149176197
-
-
M. Nishizawa, H. Imagawa, H. Yamamoto, Org. Biomol. Chem. 2010, 8, 511-521.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 511-521
-
-
Nishizawa, M.1
Imagawa, H.2
Yamamoto, H.3
-
22
-
-
0034596449
-
-
M. Okada, S. Iwashita, N. Koizumi, Tetrahedron Lett. 2000, 41, 7047-7051.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 7047-7051
-
-
Okada, M.1
Iwashita, S.2
Koizumi, N.3
-
23
-
-
79954588248
-
-
Recent reports on the reaction using sulfamate derivatives
-
Recent reports on the reaction using sulfamate derivatives
-
-
-
-
25
-
-
78649616876
-
-
Angew. Chem. Int. Ed. 2010, 49, 1634
-
S. Beaumont, V. Pons, P. Retailleau, R. H. Dodd, P. Dauban, Angew. Chem. 2010, 122, 1678; Angew. Chem. Int. Ed. 2010, 49, 1634.
-
(2010)
Angew. Chem.
, vol.122
, pp. 1678
-
-
Beaumont, S.1
Pons, V.2
Retailleau, P.3
Dodd, R.H.4
Dauban, P.5
-
26
-
-
77956459709
-
-
F. J. Wyszynski, A. L. Thompson, B. G. Davis, Org. Biomol. Chem. 2010, 8, 4246.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 4246
-
-
Wyszynski, F.J.1
Thompson, A.L.2
Davis, B.G.3
-
27
-
-
77951192304
-
-
S. Hanessian, S. Guesné, E. Chénard, Org. Lett. 2010, 12, 1816.
-
(2010)
Org. Lett.
, vol.12
, pp. 1816
-
-
Hanessian, S.1
Guesné, S.2
Chénard, E.3
-
28
-
-
71949117041
-
-
Angew. Chem. Int. Ed. 2009, 48, 2777
-
T. Kurokawa, M. Kim, J. Du Bois, Angew. Chem. 2009, 121, 2815; Angew. Chem. Int. Ed. 2009, 48, 2777.
-
(2009)
Angew. Chem.
, vol.121
, pp. 2815
-
-
Kurokawa, T.1
Kim, M.2
Du Bois, J.3
-
29
-
-
67849128913
-
-
B. M. Trost, S. Malhotra, D. E. Olson, A. Maruniak, J. Du Bois, J. Am. Chem. Soc. 2009, 131, 4190-4191.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4190-4191
-
-
Trost, B.M.1
Malhotra, S.2
Olson, D.E.3
Maruniak, A.4
Du Bois, J.5
-
31
-
-
34547913768
-
-
J. J. Fleming, M. D. McReynolds, J. Du Bois, J. Am. Chem. Soc. 2007, 129, 9964-9975.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9964-9975
-
-
Fleming, J.J.1
McReynolds, M.D.2
Du Bois, J.3
-
32
-
-
33646438818
-
-
M. Kim, J. V. Mulcahy, C. G. Espino, J. Du Bois, Org. Lett. 2006, 8, 1073-1076.
-
(2006)
Org. Lett.
, vol.8
, pp. 1073-1076
-
-
Kim, M.1
Mulcahy, J.V.2
Espino, C.G.3
Du Bois, J.4
-
33
-
-
33750476666
-
-
K. Guthikonda, P. M. Wehn, B. J. Caliando, J. Du Bois, Tetrahedron 2006, 62, 11331-11342.
-
(2006)
Tetrahedron
, vol.62
, pp. 11331-11342
-
-
Guthikonda, K.1
Wehn, P.M.2
Caliando, B.J.3
Du Bois, J.4
-
34
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79954600375
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When optically active alcohol 5 (97%âee) and 7a were used, racemic product 8a was obtained
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When optically active alcohol 5 (97%âee) and 7a were used, racemic product 8a was obtained.
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-
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35
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79954610129
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2 catalytic conditions (cf. Supporting Information, pilot study-3)
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2 catalytic conditions (cf. Supporting Information, pilot study-3).
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-
-
36
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79954608269
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Derivative 12 is unstable under acidic conditions. During column chromatography on silica gel 12 decomposed into 14
-
Derivative 12 is unstable under acidic conditions. During column chromatography on silica gel 12 decomposed into 14.
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-
-
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37
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79954598397
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The relative stereochemistry of tert-butyl ester 16 was established by NOESY experiments (cf. Supporting Information)
-
The relative stereochemistry of tert-butyl ester 16 was established by NOESY experiments (cf. Supporting Information).
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38
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60149098436
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Angew. Chem. Int. Ed. 2009, 48, 1244 - 1247
-
H. Yamamoto, I. Sasaki, Y. Hirai, K. Namba, H. Imagawa, M. Nishizawa, Angew. Chem. 2009, 121, 1270; Angew. Chem. Int. Ed. 2009, 48, 1244-1247.
-
(2009)
Angew. Chem.
, vol.121
, pp. 1270
-
-
Yamamoto, H.1
Sasaki, I.2
Hirai, Y.3
Namba, K.4
Imagawa, H.5
Nishizawa, M.6
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39
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79954604089
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Note
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The catalytic activity of recovered 17 was investigated by analyzing the same reaction of 5 with 7a to give 8a. The recycled catalyst displayed complete catalytic activity until the fourth reaction. However, a longer reaction time was required for the fifth reaction (cf. Supporting Information).
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