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13
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0026658420
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Compound 19 was prepared from the corresponding alcohol, which was obtained from the commercially available methyl (S)-(+)-3-hydroxy-2-methyl propionate in a series of reactions as described for its enantiomer (see: Diez-Martin, D.; Kotecha, N. R.; Ley, S. V.; Mantegani, S.; Menendez, J. C.; Organ, H. M.; White, A. D. Tetrahedron 1992, 48, 7899).
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Compound 19 was prepared from the corresponding alcohol, which was obtained from the commercially available methyl (S)-(+)-3-hydroxy-2-methyl propionate in a series of reactions as described for its enantiomer (see: Diez-Martin, D.; Kotecha, N. R.; Ley, S. V.; Mantegani, S.; Menendez, J. C.; Organ, H. M.; White, A. D. Tetrahedron 1992, 48, 7899).
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18
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34250829978
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The lowest energy conformation of compounds 27a (107.62 kcal/ mol) and 28 (71.20/kmol) was calculated with use of the Chem3D MM2 program.
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The lowest energy conformation of compounds 27a (107.62 kcal/ mol) and 28 (71.20/kmol) was calculated with use of the Chem3D MM2 program.
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20
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1642334165
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21
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2942564141
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Odriozola, J.M.6
Bañuelos, P.7
Tello, M.8
Linden, A.9
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23
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0028085467
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Modified Corey - Nicolaou method: Buszek, K. R.; Sato, N.; Jeong, Y. J. Am. Chem. Soc. 1994, 116, 5511.
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(b) Modified Corey - Nicolaou method: Buszek, K. R.; Sato, N.; Jeong, Y. J. Am. Chem. Soc. 1994, 116, 5511.
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