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79952159026
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2, 0 °C, 3 h) uniformly gave an approximately 1:2:1 mixture of 2, 33, and 34, formation of these isomers during acid treatment of 32 could be ascribed to thermodynamic equilibration.
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2, 0 °C, 3 h) uniformly gave an approximately 1:2:1 mixture of 2, 33, and 34, formation of these isomers during acid treatment of 32 could be ascribed to thermodynamic equilibration.
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79952175673
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In the present study, we could only isolate natural (11 S)-spiroacetal 2 as a minor product. However, we expect that we would be able to control the C11 stereochemistry in a real system by constructing the macrocyclic framework of 1 prior to spiroacetalization.
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In the present study, we could only isolate natural (11 S)-spiroacetal 2 as a minor product. However, we expect that we would be able to control the C11 stereochemistry in a real system by constructing the macrocyclic framework of 1 prior to spiroacetalization.
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