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Zhang, J.2
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Pirrung, M. C.; Zhang, J. Tetrahedron Lett. 1992, 33, 5987. For a related chiral Rh(II) phosphate catalyst reported contemporaneously by McKervey, see: McCarthy, N.; McKervey, M. A.; Ye, T.; McCann, M.; Murphy, E.; Doyle, M. P. Tetrahedron Lett. 1992, 33, 5983.
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18
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0034730008
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up to 93% ee using DMAD
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Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Tetrahedron Lett. 2000, 41, 5931 (up to 93% ee using DMAD); Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A. J. Am. Chem. Soc. 2002, 124, 14836 (up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination).
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0037132621
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up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination
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Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Tetrahedron Lett. 2000, 41, 5931 (up to 93% ee using DMAD); Suga, H.; Inoue, K.; Inoue, S.; Kakehi, A. J. Am. Chem. Soc. 2002, 124, 14836 (up to 98% ee using an 3-acryloyl-2-oxazolidinone with a chiral Lewis acid-Rh catalyst combination).
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, pp. 14836
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Suga, H.1
Inoue, K.2
Inoue, S.3
Kakehi, A.4
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0009521808
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Padwa, A.; Carter, S. P.; Nimmesgern, H.; Stull, P. D. J. Am. Chem. Soc. 1988, 110, 2894.
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21
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3242719230
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note
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No satisfactory analytical method could be found for resolving the cycloadduct from corresponding ethyl ester.
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