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A two-step stereoselective strategy for converting glycine-derived aminoesters into unnatural cyclic amino acids has been reported. The process involves a palladium-catalysed tandem allylic amination/[2,3]-Stevens rearrangement followed by a ruthenium-catalysed ring-closing metathesis (Scheme 175). " ... [Pg.585]

See other pages where Aminoesters, glycine-derived is mentioned: [Pg.293] [Pg.293] [Pg.293] [Pg.293] [Pg.206] [Pg.180]

See also in sourсe #XX -- [ Pg.293 , Pg.294 ]

See also in sourсe #XX -- [ Pg.585 ]

See also in sourсe #XX -- [ Pg.293 , Pg.294 ]