Issue 24, 1988

Decarboxylative incorporation of α-oxobutyrate and α-oxovalerate into (R)-α-hydroxyethyl- and n-propyl ketones on reaction with aromatic and α,β-unsaturated aldehydes in Baker's yeast

Abstract

Decarboxylative incorporation of linear C3, C4, and C5α-oxo acids into (R)α-hydroxy ketones (2), (9) and (10) is observed when benzaldehyde (1) is incubated with baker's yeast; α,β-unsaturated aldehydes (11) and (15) with the C3 and C4 acids yield (R)-α-hydroxy methyl and ethyl ketones (16), (20), (19), and (21).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1619-1621

Decarboxylative incorporation of α-oxobutyrate and α-oxovalerate into (R)-α-hydroxyethyl- and n-propyl ketones on reaction with aromatic and α,β-unsaturated aldehydes in Baker's yeast

C. Fuganti, P. Grasselli, G. Poli, S. Servi and A. Zorzella, J. Chem. Soc., Chem. Commun., 1988, 1619 DOI: 10.1039/C39880001619

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