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79956102061
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note
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17
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79956111410
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The X-ray crystal structural study of a derivative of compound 3 (4-(3,4-dich loro-5-methox yphenyl)-6-dim ethoxymet hyl-2-methyl-1,4-di hydropyridi ne-3,5-dicarbox ilic acid cinnamyl ester) showed that the enantiomer synthesized using l-Val-O-tBu is as a (R)-isomer (unpublished data)
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The X-ray crystal structural study of a derivative of compound 3 (4-(3,4-dichloro-5-methoxyphenyl)-6-dimethoxymethyl-2-methyl-1, 4-dihydropyridine-3,5-dicarboxilic acid cinnamyl ester) showed that the enantiomer synthesized using l-Val-O-tBu is as a (R)-isomer (unpublished data).
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18
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79956125826
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note
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Due to peak broadening in chiral HPLC conditions, the optical purify of nether (+)- nor (-)-3 could be directly determined. However, a derivative of compound 3 (4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid cinnamyl ester) was obtained with 96.0% ee using same synthetic procedure (unpublished data), implying that the hydrolysis step induces negligible racemization at the C-4 position.
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19
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0141927456
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