-
1
-
-
0036403443
-
-
For a review on atropisomerism see: Mikami, K.; Aikawa, K.; Yusa, Y.; Jodry, J. J.; Yamanaka, M. Synlett 2002, 1561.
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Synlett
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Mikami, K.1
Aikawa, K.2
Yusa, Y.3
Jodry, J.J.4
Yamanaka, M.5
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2
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29444437987
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See, for example: (a) Mata, Y.; Diéguez, M.; Pàmies, O.; Claver, C. Org. Lett. 2005, 7, 5597.
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Mata, Y.1
Diéguez, M.2
Pàmies, O.3
Claver, C.4
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4
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18844381406
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(c) Reetz, M. T.; Li, X. Angew. Chem., Int. Ed. 2005, 44, 2959.
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Angew. Chem., Int. Ed.
, vol.44
, pp. 2959
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Reetz, M.T.1
Li, X.2
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5
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-
20444391382
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(d) Duursma, A.; Peña, D.; Minnaard, A. J.; Feringa, B. L. Tetrahedron: Asymmetry 2005, 16, 1901.
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Tetrahedron: Asymmetry
, vol.16
, pp. 1901
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Duursma, A.1
Peña, D.2
Minnaard, A.J.3
Feringa, B.L.4
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6
-
-
27644546852
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-
See, for example: (a) Leitner, A.; Shekhar, S.; Pouy, M. J.; Hartwig, J. F. J. Am. Chem. Soc. 2005, 127, 15506.
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J. Am. Chem. Soc.
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Leitner, A.1
Shekhar, S.2
Pouy, M.J.3
Hartwig, J.F.4
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7
-
-
0042510143
-
-
(b) Shum, S. P.; Pastor, S. D.; DeBellis, A. D.; Odorisio, P. A.; Burke, L.; Clarke, F. H.; Rihs, G.; Piatek, B.; Rodebaugh, R. K. Inorg. Chem. 2003, 42, 5097.
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Inorg. Chem.
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, pp. 5097
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Shum, S.P.1
Pastor, S.D.2
Debellis, A.D.3
Odorisio, P.A.4
Burke, L.5
Clarke, F.H.6
Rihs, G.7
Piatek, B.8
Rodebaugh, R.K.9
-
8
-
-
0001670062
-
-
(c) Pastor, S. D.; Shum, S. P.; Rodebaugh, R. K.; DeBellis, A. D. Helv. Chim. Acta 1993, 76, 900.
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, pp. 900
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Pastor, S.D.1
Shum, S.P.2
Rodebaugh, R.K.3
DeBellis, A.D.4
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9
-
-
84976254301
-
-
(a) Hoppe, I.; Hoppe, D.; Wolff, C.; Egert, E.; Herbst, R. Angew. Chem., Int. Ed. Engl. 1989, 28, 67.
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Hoppe, I.1
Hoppe, D.2
Wolff, C.3
Egert, E.4
Herbst, R.5
-
10
-
-
0026323731
-
-
(b) Hoppe, I.; Hoffmann, H.; Gärtner, I.; Krettek, T.; Hoppe, D. Synthesis 1991, 1157.
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(1991)
Synthesis
, pp. 1157
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Hoppe, I.1
Hoffmann, H.2
Gärtner, I.3
Krettek, T.4
Hoppe, D.5
-
13
-
-
0027169226
-
-
(a) Buisman, G. J. H.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Tetrahedron: Asymmetry 1993, 4, 1625.
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(1993)
Tetrahedron: Asymmetry
, vol.4
, pp. 1625
-
-
Buisman, G.J.H.1
Kamer, P.C.J.2
Van Leeuwen, P.W.N.M.3
-
14
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-
84989457054
-
-
(b) Yamato, T.; Hasegawa, K.; Saruwatari, Y.; Doamekpor, L. Chem. Ber. 1993, 126, 1435.
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Yamato, T.1
Hasegawa, K.2
Saruwatari, Y.3
Doamekpor, L.4
-
16
-
-
24144466864
-
-
(b) Kauch, M.; Snieckus, V.; Hoppe, D. J. Org. Chem. 2005, 70, 7149.
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Kauch, M.1
Snieckus, V.2
Hoppe, D.3
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17
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33745528323
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-
note
-
CD-spectroscopic and quantum chemical investigations on a related compound support this assumption; in cooperation with C. Diedrich and S. Grimme. To be published.
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-
-
-
18
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-
0037033561
-
-
In our work using chiral N-arenesulfonyl-1,3-oxazolidines as chiral auxiliaries, nor-pseudoephedrine derivatives often provided superior selectivity; see, for example: Brüggemann, M.; Fröhlich, R.; Wibbeling, B.; Holst, C.; Hoppe, D. Tetrahedron 2002, 58, 321.
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(2002)
Tetrahedron
, vol.58
, pp. 321
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Brüggemann, M.1
Fröhlich, R.2
Wibbeling, B.3
Holst, C.4
Hoppe, D.5
-
21
-
-
0027144045
-
-
The absolute configuration of 12 was determined by derivatization: Alexakis, A.; Frutos, J. C.; Mangeney, P. Tetrahedron: Asymmetry 1993, 4, 2431.
-
(1993)
Tetrahedron: Asymmetry
, vol.4
, pp. 2431
-
-
Alexakis, A.1
Frutos, J.C.2
Mangeney, P.3
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