Chiral propionate enolate equivalent for stereoselective additions to symmetrical ketones |
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Authors: | Philip W Ambler Stephen G Davies |
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Institution: | The Dyson Perrins Laboratory, South Parks Road. Oxford. OX1 3QY. U.K. |
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Abstract: | The copper enolate derived from (η5-C5H5)Fe(CO)(PPh3)COCH2CH3 reacts stereoselectively with symmetrical ketones to generate RR,SS-α-methyl-β-hydroxy acyl complexes which on decomplexation liberate the corresponding β-hydroxy acids. |
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