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- W2058144489 abstract "An asymmetric synthesis of a key intermediate 16 to (+)-lactacystin 1 has been established starting from epoxide 2 via intramolecular mercurioamidation of allylic trichloroacetimidate 4 and concomitant addition-reduction of ester 13 by Pri MgBr, in which reduction of the intermediate ketone proceeded with complete stereoselectivity." @default.
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- W2058144489 date "1998-01-01" @default.
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- W2058144489 title "An enantiocontrolled synthesis of a key intermediate to (+)-lactacystin" @default.
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