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- W2952040752 abstract "Aza-conjugate addition of the lithium anion of N-trimethylsilyl-p-methoxybenzylamine to tert-butyl enoate acceptors, in the presence of a stoichiometric amount of enantiopure 1,2-dimethoxy-1,2-diphenylethane and excess trimethylsilyl chloride, affords tert-butyl-N-p-methoxybenzyl-β-amino esters with excellent levels of enantiocontrol. These N-p-methoxybenzyl-β-amino-esters may be deprotected under oxidative conditions via treatment with ceric ammonium nitrate, followed by acid hydrolysis of the resultant imine intermediates, to afford enantiopure β-amino-esters containing hydrogenolytically sensitive functionality." @default.
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- W2952040752 date "2016-02-01" @default.
- W2952040752 modified "2023-09-23" @default.
- W2952040752 title "ChemInform Abstract: A Chiral Ligand Mediated Aza-Conjugate Addition Strategy for the Enantioselective Synthesis of β-Amino Esters that Contain Hydrogenolytically Sensitive Functionality." @default.
- W2952040752 cites W2218287179 @default.
- W2952040752 doi "https://doi.org/10.1002/chin.201608026" @default.
- W2952040752 hasPublicationYear "2016" @default.
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