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Total Synthesis of Bryostatin 2 Evans

The synthesis of the BC-ring fragment 26 begins with the enantioselective aldol reaction of aldehyde 22 and chiral boron enolate 23 derived from (—)-DIP-Cl as described by Paterson and Brown [42]. The aldol adduct 24 is converted to the [Pg.110]

3 Steps including hydroxy directed reduction of C3 ketone [Pg.111]

4 Steps including hydroxy directed diastereoselective Tischenko reaction [Pg.111]

11 Steps including hydroxy directed alkyne hydroalumination-iodination [Pg.113]


See other pages where Total Synthesis of Bryostatin 2 Evans is mentioned: [Pg.110]   


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Evans synthesis

Total Synthesis of

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