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Oxazolidinone enoates

Scheme 65 Addition/allylation of enoates derived from oxazolidinones... Scheme 65 Addition/allylation of enoates derived from oxazolidinones...
Success in diastereoselective Lewis acid-mediated conjugate radical additions using chiral oxazolidinones led Sibi and Porter to evaluate enantioselective variants. Based on previous work from their laboratories as well as information in the literature (control of the s-cis vs s-trans rotamer of the enoate), they surmised that a bidentate Lewis acid in combination with an achiral oxazolidinone template and a chiral ligand would be a good starting point to probe enantioselective conjugate radical additions (Scheme 2). [Pg.470]

See other pages where Oxazolidinone enoates is mentioned: [Pg.563]    [Pg.71]    [Pg.414]    [Pg.563]    [Pg.71]    [Pg.414]    [Pg.38]    [Pg.455]    [Pg.455]    [Pg.455]    [Pg.321]    [Pg.268]    [Pg.202]    [Pg.333]    [Pg.56]   
See also in sourсe #XX -- [ Pg.71 ]



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Enoates

Oxazolidinone

Oxazolidinones

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