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note
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In the absence of BBTO, the regioisomers 4 and 5 were obtained in only 20% isolated yield, recovering 80% of the starting styrene oxide.
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24
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19444376032
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note
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In the ring-opening reactions of (R) styrene oxide catalyzed by 3, the study of the enantiomeric excess was done only with stereoisomers 4a and 4b, since 2-isopropoxy-2-phenylethanol (6) was isolated in low yield.
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