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0030739191
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11944249437
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For reviews, see: (a) Cha, J. K.; Kim, N.-S. Chem. Rev. 1995, 95, 1761-1795; (b) Cha, J. K.; Christ, W. J.; Kishi, Y. Tetrahedron 1984, 40, 2247-2255.
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For reviews, see: (a) Cha, J. K.; Kim, N.-S. Chem. Rev. 1995, 95, 1761-1795; (b) Cha, J. K.; Christ, W. J.; Kishi, Y. Tetrahedron 1984, 40, 2247-2255.
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10
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0033617137
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The predominant syn selectivity with the cyclic amides was obtained by addition of TMEDA. See: Donohoe T.J., Blades K., Helliwell M., Moore P.R., Winter J.J.G. J. Org. Chem. 64:1999;2980-2981. and references cited therein.
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0030599656
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For recent examples, see: (a) Reetz, M. T.; Strack, T. J.; Mutulis, F.; Goddard, R. Tetrahedron Lett. 1996, 37, 9293-9296; (b) Brånalt, J.; Kvarnström, I.; Classon, B.; Samuelsson, B.; Nillroth, U.; Danielson, U. H.; Karlén, A.; Hallberg, A. Tetrahedron Lett. 1997, 38, 3483-3486.
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For recent examples, see: (a) Reetz, M. T.; Strack, T. J.; Mutulis, F.; Goddard, R. Tetrahedron Lett. 1996, 37, 9293-9296; (b) Brånalt, J.; Kvarnström, I.; Classon, B.; Samuelsson, B.; Nillroth, U.; Danielson, U. H.; Karlén, A.; Hallberg, A. Tetrahedron Lett. 1997, 38, 3483-3486.
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Hallberg, A.8
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14
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0028210914
-
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and references cited therein
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The syn selectivity was reported with the N-Boc allylic amino olefins, and the Z-disubstituted olefin with several different allylic amides or carbamates in i-PrOH. See: Krysan D.J., Rockway T.W., Haight A.R. Tetrahedron: Asymmetry. 5:1994;625-632. and references cited therein.
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17
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0010556273
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M.E. Thesis, Seoul National University, Feb.
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The selectivities with N-trichloroacetamide, N-benzoyl, N-Boc, and N,N-dibenzyl derivatives for the dihydroxylation reactions of a monosubstituted olefin in aqueous THF were about 1:1-1.3:1. See: Yoon, S. W. M.E. Thesis, Seoul National University, Feb. 1997.
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Yoon, S.W.1
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20
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0000711829
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For use of the benzophenone ketimine derivatives in the enantioselective dihydroxylation reactions of allylamine, see: (a) Corey, E. J.; Guzman, P. A.; Noe, M. C. J. Am. Chem. Soc. 1995, 117, 10805-10816. For the ketimines as a protecting group, see: (b) Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; John Wiley & Sons: New York, 1999; pp. 587-590.
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For use of the benzophenone ketimine derivatives in the enantioselective dihydroxylation reactions of allylamine, see: (a) Corey, E. J.; Guzman, P. A.; Noe, M. C. J. Am. Chem. Soc. 1995, 117, 10805-10816. For the ketimines as a protecting group, see: (b) Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; John Wiley & Sons: New York, 1999; pp. 587-590.
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0001582498
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Each amino acid, alanine, phenylalanine and valine, was converted to 24, 25 and 26, respectively, based on the following protocol. See: Luly J.R., Dellaria J.F., Plattner J.J., Soderquist J.L., Yi N. J. Org. Chem. 52:1987;1487-1492.
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