Topic
Aldose
About: Aldose is a research topic. Over the lifetime, 1270 publications have been published within this topic receiving 27197 citations. The topic is also known as: aldoses.
Papers published on a yearly basis
Papers
More filters
•
26 Nov 1997TL;DR: In this article, the process for producing an aldose or aldoses derivative containing n carbon atoms is described, which involves: (a) contacting an aqueous solution of a sugar acid having n+1 carbon atoms and containing at least one alpha-hydroxy acid unit, or a salt thereof, with hydrogen peroxide in the presence of a copper salt; (b) separating precipitated copper; (c) regenerating the copper salt with the corresponding acid; and (d) recycling the regenerated salt.
Abstract: Process for producing an aldose or aldose derivative containing n carbon atoms comprises: (a) contacting an aqueous solution of a sugar acid having n+1 carbon atoms and containing at least one alpha -hydroxy acid unit, or a salt thereof, with hydrogen peroxide in the presence of a copper salt; (b) separating precipitated copper; (c) regenerating the copper salt with the corresponding acid; and (d) recycling the regenerated salt. The aqueous solution contains 1-60 wt.% of the sugar acid. The Cu salt is used in an amount of 0.01-50% based on the sugar acid. The H2O2 has a concentration of 35-70% and is used in an amount of 1-500 mole% based on the sugar acid. The reaction is effected at 0-100 deg C, especially 15-40 deg C, and pH 5-9, especially 6-8. The sugar acid is arabinonic acid, optionally in Na or Ca salt form. The copper salt is CuSO4 and is regenerated with H2SO4.
2 citations
••
TL;DR: Cord factor analogs were regioselectively synthesized by reactions of unprotected α, α-D-trehalose with long-chain acyl chlorides through tributylstannylation in good yields as discussed by the authors.
Abstract: Cord factor analogs were regioselectively synthesized by reactions of unprotected α, α-D-trehalose with long-chain acyl chlorides through tributylstannylation in good yields.
2 citations
••
2 citations
•
2 citations
••
TL;DR: In this paper, the reaction of D-arabinose diethyl dithioacetal with one equivalent of benzaldehyde dimethyl acetal in the presence of p-toluenesulfonic acid at −40 °C gave a mixture of the two epimers of 5-Omethoxy.
Abstract: Reaction of D-arabinose diethyl dithioacetal with one equivalent of benzaldehyde dimethyl acetal in the presence of p-toluenesulfonic acid at −40 °C gave a mixture of the two epimers of 5-O-methoxy...
2 citations