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1
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0003445429
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Springer, Berlin
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a) E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Comprehensive Asymmetric Catalysis I-III, Vol. 3, Springer, Berlin, 1999;
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Jacobsen, E.N.1
Pfaltz, A.2
Yamamoto, H.3
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4
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0036263839
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Angew. Chem. Int. Ed. 2002, 41, 1650.
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17744393466
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M. P. Sibi, Z. Ma, C. P. Jasperse, J. Am. Chem. Soc. 2005, 127, 5764.
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Sibi, M.P.1
Ma, Z.2
Jasperse, C.P.3
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6
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33646567185
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An example of the non-asymmetric variant was previously reported: R. Shintani, T. Hayashi, J. Am. Chem. Soc. 2006, 128, 6330
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An example of the non-asymmetric variant was previously reported: R. Shintani, T. Hayashi, J. Am. Chem. Soc. 2006, 128, 6330.
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9
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0012850032
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For a review, see, Eds, S. Kobayashi, K. A. Jørgensen, Wiley-VCH, Weinheim
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For a review, see D. M. T. Chan in Cycloaddition Reactions in Organic Synthesis (Eds.: S. Kobayashi, K. A. Jørgensen), Wiley-VCH, Weinheim, 2002, p. 57.
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Cycloaddition Reactions in Organic Synthesis
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Chan, D.M.T.1
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A. Yamamoto, Y. Ito, T. Hayashi, Tetrahedron Lett. 1989, 30, 375.
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Yamamoto, A.1
Ito, Y.2
Hayashi, T.3
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11
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33750053278
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B. M. Trost, J. P. Stambuli, S. M. Silverman, U. Schwörer, J. Am. Chem. Soc. 2006, 128, 13 328.
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J. Am. Chem. Soc
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Trost, B.M.1
Stambuli, J.P.2
Silverman, S.M.3
Schwörer, U.4
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13
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0034815578
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b) S. J. Hedley, W. J. Moran, A. H. G. P. Prenzel, D. A. Price, J. P. A. Harrity, Synlett 2001, 1596;
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Hedley, S.J.1
Moran, W.J.2
Prenzel, A.H.G.P.3
Price, D.A.4
Harrity, J.P.A.5
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14
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0038441546
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c) S. J. Hedley, W. J. Moran, D. A. Price, J. P. A. Harrity, J. Org. Chem. 2003, 68, 4286;
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Hedley, S.J.1
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Price, D.A.3
Harrity, J.P.A.4
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15
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11844292757
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d) K. M. Goodenough, W. J. Moran, P. Raubo, J. P. A. Harrity, J. Org. Chem. 2005, 70, 207.
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Goodenough, K.M.1
Moran, W.J.2
Raubo, P.3
Harrity, J.P.A.4
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16
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34547748975
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3 shows no reactivity.
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3 shows no reactivity.
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17
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34547729760
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For examples of metal-catalyzed synthesis of 1,2-oxazines, see a I. S. Young, M. A. Kerr, Angew. Chem. 2003, 115, 3131;
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For examples of metal-catalyzed synthesis of 1,2-oxazines, see a) I. S. Young, M. A. Kerr, Angew. Chem. 2003, 115, 3131;
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18
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0041806585
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Angew. Chem. Int. Ed. 2003, 42, 3023;
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Angew. Chem. Int. Ed. 2005, 44, 7832;
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Chem. Int. Ed
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34547754043
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Ref, 2
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c) Ref. [2].
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B. M. Trost, T. N. Nanninga, T. Satoh, J. Am. Chem. Soc. 1985, 107, 721.
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Trost, B.M.1
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Satoh, T.3
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24
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0001514035
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b) Y. Uozumi, A. Tanahashi, S.-Y. Lee, T. Hayashi, J. Org. Chem. 1993, 58, 1945.
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Uozumi, Y.1
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Lee, S.-Y.3
Hayashi, T.4
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25
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0011404010
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H. Takaya, K. Mashima, K. Koyano, M. Yagi, H. Kumobayashi, T. Taketomi, S. Akutagawa, R. Noyori, J. Org. Chem. 1986, 51, 629.
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Takaya, H.1
Mashima, K.2
Koyano, K.3
Yagi, M.4
Kumobayashi, H.5
Taketomi, T.6
Akutagawa, S.7
Noyori, R.8
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26
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0034725134
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L. A. Arnold, R. Imbos, A. Mandoli, A. H. M. de Vries, R. Zaasz, B. L. Feringa, Tetrahedron 2000, 56, 2865.
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Tetrahedron
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Arnold, L.A.1
Imbos, R.2
Mandoli, A.3
de Vries, A.H.M.4
Zaasz, R.5
Feringa, B.L.6
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27
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0000766561
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B. L. Feringa, M. Pineschi, L. A. Arnold, R. Imbos, A. H. M. de Vries, Angew. Chem. 1997, 109, 2733;
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Feringa, B.L.1
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Arnold, L.A.3
Imbos, R.4
de Vries, A.H.M.5
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29
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0037100318
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The diastereomer of this compound ((S,R,R)-6c) has been reported: a) A. Duursma, A. J. Minnaard, B. L. Feringa, Tetrahedron 2002, 58, 5773;
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The diastereomer of this compound ((S,R,R)-6c) has been reported: a) A. Duursma, A. J. Minnaard, B. L. Feringa, Tetrahedron 2002, 58, 5773;
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30
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2342660181
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b) A. W. van Zijl, L. A. Arnold, A. J. Minnaard, B. L. Feringa, Adv. Synth. Catal. 2004, 346, 413.
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Adv. Synth. Catal
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van Zijl, A.W.1
Arnold, L.A.2
Minnaard, A.J.3
Feringa, B.L.4
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31
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1642578965
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A. Alexakis, S. Gille, F. Prian, S. Rosset, K. Ditrich, Tetrahedron Lett. 2004, 45, 1449.
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Tetrahedron Lett
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Alexakis, A.1
Gille, S.2
Prian, F.3
Rosset, S.4
Ditrich, K.5
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32
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34547815652
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Alkyl-substituted nitrones are not suitable substrates under the present reaction conditions; they give little or no cycloadducts
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Alkyl-substituted nitrones are not suitable substrates under the present reaction conditions; they give little or no cycloadducts.
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