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Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, Chapter 7.2
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(a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
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(a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
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Oishi, M.2
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0000448986
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(a) For a thermal Bamford-Stevens reaction using an aziridinyl imine, see: Mohamadi, F.; Collum, D. B. Tetrahedron Lett. 1984, 25, 271. For Shapiro reactions of aziridinyl imines, see: (b) Maruoka, K.; Oishi, M.; Yamamoto, H. J. Am. Chem. Soc. 1996, 118, 2289. (c) Evans, D. A.; Nelson, J. V. J. Am. Chem. Soc. 1980, 102, 774.
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Evans, D.A.1
Nelson, J.V.2
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0001589182
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N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
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Padwa, A.1
Austin, D.J.2
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Kassir, J.M.4
Xu, S.L.5
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15
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37049076140
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N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
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Sarkar, T.K.1
Ghorai, B.K.2
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16
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0025303985
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N-aziridinyl imines in combination with catalysis have seen limited use. For examples, see: (a) Padwa, A.; Austin, D. J.; Gareau, Y.; Kassir, J. M.; Xu, S. L. J. Am. Chem. Soc. 1993, 115, 2637. (b) Sarkar, T. K.; Ghorai, B. K. J. Chem. Soc., Chem. Commun. 1992, 1184. (c) Fang, F. G.; Maier, M. E.; Danishefsky, S. J.; Schulte, G. J. Org. Chem. 1990, 55, 831.
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Fang, F.G.1
Maier, M.E.2
Danishefsky, S.J.3
Schulte, G.4
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17
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0010963938
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note
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All hydrazones were prepared from the corresponding ketones. See the Supporting Information.
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18
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0001031980
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(a) Taber, D. F.; Herr, R. J.; Pack, S. K.; Geremia, J. M. J. Org. Chem. 1996, 61, 2908.
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Taber, D.F.1
Herr, R.J.2
Pack, S.K.3
Geremia, J.M.4
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20
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0010968399
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See refs 3b and 8b
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(c) See refs 3b and 8b.
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21
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0033518872
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For an alternative rhodium carbenoid-initiated Claisen rearrangement, see: Wood, J. L.; Moniz, G. A.; Pflum, D. A.; Stoltz, B. M.; Holubec, A. A.; Dietrich, H.-J. J. Am. Chem. Soc. 1999, 121, 1748.
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Wood, J.L.1
Moniz, G.A.2
Pflum, D.A.3
Stoltz, B.M.4
Holubec, A.A.5
Dietrich, H.-J.6
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23
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0025355715
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(b) Nonoshita, K.; Banno, H.; Maruoka, K.; Yamamoto, H. J. Am. Chem. Soc. 1990, 112, 316.
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Nonoshita, K.1
Banno, H.2
Maruoka, K.3
Yamamoto, H.4
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24
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0021376573
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(c) Takai, K.; Mori, I.; Oshima, K.; Nozaki, H. Bull. Chem. Soc. Jpn. 1984, 57, 446.
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Takai, K.1
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Nozaki, H.4
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25
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0001403390
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For a similar ene reaction, see: Corey, E. J.; Roberts, B. E.; Dixon, B. R. J. Am. Chem. Soc. 1995, 117, 193.
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J. Am. Chem. Soc.
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Corey, E.J.1
Roberts, B.E.2
Dixon, B.R.3
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