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A simple racemization-free procedure allows the regeneration of the carboxylic acid group of amino acid alkyl esters by way of an intermediate 5-oxazolidinone which is hydrolyzed by treatment with sodium hydrogen carbonate in aqueous methanol

Mild regeneration of the carboxylic group of amino acid alkyl esters by aqueous methanolic sodium hydrogen carbonate via 5-oxazolidinones / P. Allevi, M. Anastasia. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 44:41(2003 Oct 06), pp. 7663-7665.

Mild regeneration of the carboxylic group of amino acid alkyl esters by aqueous methanolic sodium hydrogen carbonate via 5-oxazolidinones

P. Allevi
Primo
;M. Anastasia
Ultimo
2003

Abstract

A simple racemization-free procedure allows the regeneration of the carboxylic acid group of amino acid alkyl esters by way of an intermediate 5-oxazolidinone which is hydrolyzed by treatment with sodium hydrogen carbonate in aqueous methanol
Protecting groups ; biochemical interest ; Michael-acceptor ; butyl esters ; transformation ; glycopeptides ; pyridinoline ; deblocking
Settore BIO/10 - Biochimica
6-ott-2003
TETRAHEDRON LETTERS
Article (author)
01 - Articolo su periodico
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/27938
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