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A-Aminocarboxylic acids esters

Oxaziridines are oxidizing agents as well as important synthetic intermediates [21]. For instance, iV-hydroxyaminocarboxylic esters 2 can be prepared from a-aminocarboxylic acid esters... [Pg.34]

Sodium bis(trimethylsilyl)amide a-Aminocarboxylic acid esters from halides Synthesis with addition of 2 C-atoms... [Pg.197]

Startg. 2,3-azetidinedione added to ca. 1.4 eqs. m-chloroperoxybenzoic acid in methylene chloride at — 20°, the mixture stirred for 60 min, treated dropwise with a soln. of / r/-butylamine and pyridine in the same solvent, and stirred at room temp, for 70 min product. Y 70%. F.e. and a-aminocarboxylic acid esters with alcohols, also 3-(a-nitroalkylidene)-2-azetidinones, s. F.P. Cossio et al., Tetrahedron Letters 29, 3133-6 (1988). [Pg.44]

Sodium trihydridocyanoborate Prim, amines from N-silylimines a-Aminocarboxylic acid esters... [Pg.315]

Alkoxyenacylamines Eneurethans Enol carbamates a,P-Ethylene-a-aminocarboxylic acid esters... [Pg.546]

Sodium hydrogen carbonate a-Aminocarboxylic acid esters from aziridinones via their O-alkylation... [Pg.47]

Via intermediates a-Aminocarboxylic acid esters from a-aminocarboxylic acids via 2,5-oxazolidiones s. lA, 240 Sulfenic acid esters from sulfenic acids via sulfenylchlorides s. 13, 244... [Pg.439]

See other pages where A-Aminocarboxylic acids esters is mentioned: [Pg.230]    [Pg.430]    [Pg.257]    [Pg.248]    [Pg.346]    [Pg.347]    [Pg.14]    [Pg.270]    [Pg.272]    [Pg.284]    [Pg.79]    [Pg.212]    [Pg.311]    [Pg.448]    [Pg.77]    [Pg.87]    [Pg.332]    [Pg.473]    [Pg.20]    [Pg.62]    [Pg.127]    [Pg.356]    [Pg.366]    [Pg.247]    [Pg.262]    [Pg.271]    [Pg.493]    [Pg.185]    [Pg.274]    [Pg.362]    [Pg.240]    [Pg.256]    [Pg.24]    [Pg.172]   


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Aminocarboxylate

Aminocarboxylic acids

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