High diastereoselectivity is obtained during the addition of ethyl isocyanoacetate 1 to chiral complexes 2 and 3. The 2-oxazoline-4-carboxylic esters are intermediates for the synthesis of β-substituted serines in a stereoconservative process.

STEREOSELECTIVE SYNTHESIS OF BETA-HYDROXYAMINO ACIDS BY ALDOL REACTION OF ALPHA-ISOCYANOCARBOXYLATE WITH ARENE-CHROMIUM-TRICARBONYL COMPLEXES / S. COLONNA, A. MANFREDI, A. SOLLADIE-CAVALLO, S. QUAZZOTTI. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 31:43(1990), pp. 6185-6188.

STEREOSELECTIVE SYNTHESIS OF BETA-HYDROXYAMINO ACIDS BY ALDOL REACTION OF ALPHA-ISOCYANOCARBOXYLATE WITH ARENE-CHROMIUM-TRICARBONYL COMPLEXES

A. MANFREDI
Secondo
;
1990

Abstract

High diastereoselectivity is obtained during the addition of ethyl isocyanoacetate 1 to chiral complexes 2 and 3. The 2-oxazoline-4-carboxylic esters are intermediates for the synthesis of β-substituted serines in a stereoconservative process.
Settore CHIM/06 - Chimica Organica
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/187695
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