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and refernces cited therein
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0343786528
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Since there is no value available in the literature for the specific rotation of homochiral β-nitrostyrene adduct we were unable to assign the enantiomeric excess of the compound right away. But efforts are under way to determine ee for this and other substrates by complementary chiral HPLC analysis
-
Since there is no value available in the literature for the specific rotation of homochiral β-nitrostyrene adduct we were unable to assign the enantiomeric excess of the compound right away. But efforts are under way to determine ee for this and other substrates by complementary chiral HPLC analysis.
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-
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17
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0342915652
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According to Shibasaki the enantiomeric excess of the products have been verified by optical rotation as well as by chiral HPLC analysis. We hence based our estimation of enantiomeric exces of the adducts on the respective specific rotation value and compared it to the reported value
-
According to Shibasaki the enantiomeric excess of the products have been verified by optical rotation as well as by chiral HPLC analysis. We hence based our estimation of enantiomeric exces of the adducts on the respective specific rotation value and compared it to the reported value.
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18
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The ees of the products of Michael addition of thiols to enones reported in the literature were based on the specific rotaion values, NMR and chemical methods. We have hence calculated the ees based on the reported specific rotation values for the products
-
The ees of the products of Michael addition of thiols to enones reported in the literature were based on the specific rotaion values, NMR and chemical methods. We have hence calculated the ees based on the reported specific rotation values for the products.
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34
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0038561974
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