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TADDOL-derived phosphoramidite

A highly enantioselective synthesis of a-dehydroamino acids (186) with a stereogenic centre at the y -position has been developed, which employs a copper-catalysed asymmetric conjugate addition of diethylzinc to a,j3-unsaturated imines (185) with the TADDOL-derived phosphoramidite (187) as a chiral ligand.234... [Pg.363]

See other pages where TADDOL-derived phosphoramidite is mentioned: [Pg.129] [Pg.542] [Pg.170] [Pg.171] [Pg.430] [Pg.67] [Pg.226] [Pg.193] [Pg.438] [Pg.129] [Pg.542] [Pg.170] [Pg.171] [Pg.430] [Pg.67] [Pg.226] [Pg.193] [Pg.438] [Pg.549] [Pg.1015] [Pg.69] [Pg.207] [Pg.227] [Pg.351] [Pg.176] [Pg.373] [Pg.63] [Pg.133] [Pg.133] [Pg.99] [Pg.289] [Pg.86] [Pg.471] [Pg.213]

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Phosphoramidite

Phosphoramidite derivatives

Phosphoramidite ligands TADDOL-derived

Phosphoramidites

Phosphoramidites, TADDOL-derived

TADDOL phosphoramidite derivative

TADDOLate

TADDOLates

TADDOLs