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Synlett 1998; 1998(12): 1339-1340
DOI: 10.1055/s-1998-1972
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A Two-Step Preparation of a New C4 Chiral Building Block Derivative of D-Erythronic Acid

M. C. B. V. de Souza* , M. N. da Silva, V. F. Ferreira
  • *Universidade Federal Fluminense, Instituto de Química, CEG-GQO, Campus do Valonguinho, Niterói, CEP 24020-150, Rio de Janeiro, Brazil; Fax 55-21-620-7749; E-mail: cegvito@vm.uff.br
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Publication Date:
31 December 2000 (online)

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1,2;3,4-Di-O-isopropylidene-D-erythronic acid (2,2,2′,2′-Tetramethyl-[R,R-(4,4′-bi-1,3-dioxolan)]-5-one 4, a new C4 chiral building block derivative of D-erythronic acid was prepared in two steps from D-glucono-δ-lactone.

erythronolactone - oxidation - gluconolactone - chiral building block - erythronamide

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