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3
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12044259820
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and literature cited therein
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(c) Edge-to-face aromatic interactions have also been invoked in many examples of molecular recognition. See, for example: Paliwal, S.; Greib, S.; Wilcox, C. S. J. Am. Chem. Soc. 1994, 116, 4497-4498 and literature cited therein.
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7
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0000740681
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(a) Fustero, S.; Navarro, A.; Pina, B.; Asensio, A.; Bravo, P.; Crucianelli, M.; Volonterio, A.; Zanda, M. J. Org. Chem. 1998, 63, 6210-6219.
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Volonterio, A.7
Zanda, M.8
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8
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0002771955
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(b) Bravo, P.; Cavicchio, G.; Crucianelli, M.; Markovsky, A. L.; Volonterio, A.; Zanda, M. Synlett 1996, 887-889.
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Bravo, P.1
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Volonterio, A.5
Zanda, M.6
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9
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Crucianelli, M.; Bravo, P.; Arnone, A.; Corradi, E.; Meille, S. V.; Zanda, M. J. Org. Chem. 2000, 65, 2965-2971.
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10
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(a) Taniguchi, M.; Fujii, H.; Oshima, K.; Utimoto, K. Tetrahedron 1993, 49, 11169-11182.
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Taniguchi, M.1
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13
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0032560940
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(b) Heaton, N. J.; Bello, P.; Herradón, B.; del Campo, A.; Jiménez-Barbero, J. J. Am. Chem. Soc. 1998, 120, 9632-9645.
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14
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0000632739
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π-Stacking between aromatic rings in protic solvents have been described in the literature: (a) Kool, E. T.; Breslow, R. K. J. Am. Chem. Soc. 1988, 110, 1596-1597.
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0025088089
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(b) Schumacher, D. P.; Clark, J. E.; Murphy, B. L.; Fisher, P. A. J. Org. Chem. 1990, 55, 5291-5294.
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16
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0035825778
-
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and references therein
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An efficient catalytic asymmetric synthesis of α-amino acids has been very recently described, See: Abe, H.; Amii, H.; Uneyama, K. Org. Lett. 2001, 3, 313-315 and references therein.
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Abe, H.1
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17
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0041295494
-
-
note
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s)-5e will be published in a full account of this work.
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-
-
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18
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0032580376
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RCM has emerged as a prominent reaction for the synthesis of medium- and large-sized rings from acyclic diene precursors. See, for example: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413-4450.
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Grubbs, R.H.1
Chang, S.2
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0001811974
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RCM has been used to prepare a variety of nitrogen-containing natural products including peptidomimetics: Phillips, A. J.; Abell, A. D. Aldrichimica Acta 1999, 32, 75-89.
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Phillips, A.J.1
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0002201168
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For related systems, see: (a) Osipov, S. N.; Bruneau, Ch.; Picquet, M.; Kolomiets, A. F.; Dixneuf, P. H. Chem. Commun. 1998, 2053-2054.
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Osipov, S.N.1
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Kolomiets, A.F.4
Dixneuf, P.H.5
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23
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0033930445
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(b) Osipov, S. N.; Artyushin, O. I.; Kolomiets, A. F.; Bruneau, Ch.; Dixneuf, P. H. Synlett 2000, 1031-1033.
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Osipov, S.N.1
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Bruneau, Ch.4
Dixneuf, P.H.5
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24
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33751392007
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For the preparation of enantiopure sulfoxides 1 and imidoyl halides 2, see: (a) Fernández, I.; Khiar, N.; Llera, J. M.; Alcudia, F. J. Org. Chem. 1992, 57, 6789-6796.
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Fernández, I.1
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(b) Uneyama, K.; Tamura, K.; Mizukami, H.; Maeda, K. J. Org. Chem. 1993, 58, 32-36.
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Uneyama, K.1
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26
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0041295493
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note
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2) with NaH followed by N-alkylation of the previously isolated N-unsubstituted oxazolidinone.
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