hemiacetal

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hemiacetal

(ˌhɛmɪəˈsiːtæl)
n
any of a class of compounds derived from aldehydes by adding an alcohol to the carbonyl group
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014
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Noun1.hemiacetal - an organic compound usually formed as an intermediate product in the preparation of acetals from aldehydes or ketones
organic compound - any compound of carbon and another element or a radical
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References in periodicals archive
The results were confirmed by means of spectrophotometers analysis at the UV-visible region, were the maximum absorption band is 230 nm ([lambda]max.MeOH) corresponds to triterpenes, the bands in 280 and 330 nm (Xmax.MeOH) are for phenolic compounds and flavonoids, the band in 280 nm corresponds to the A ring absorption (hemiacetal) and the band in 370 nm represents the flavonoids B ring (Figure 2).
Polysaccharides have many functionalities, which include the capability of their hydroxyl groups and hemiacetal ends to reduce metal precursor salts [61].
To the resulting hemiacetal (1.04 g, 3 mmol), monoester 1 (0.61 g, 3 mmol), EDC (0.74 g, 3 mmol x 1.3 eq.), and catalytic amount of DMAP were added under nitrogen with C[H.sub.2][Cl.sub.2] (30 mL).
In the course of investigating nucleoside synthesis using a dehydrating reagent, glycosyl fluoride was formed as the by-product in good yield starting from the hemiacetal. In the early 1980's, the synthesis of glycosyl fluorides was a problem because preparative methods usually included the use of hazardous anhydrous hydrogen fluoride.
For flavonoid O-glycosides, heterolytic cleavage of hemiacetal O-C bond often occurs with loss of the sugar moiety.
Natural AP sites occur in equilibrium states between the hemiacetal and the aldehyde forms.
One is the ring-opening reaction of the depolymerized xylan unit through the cleavage of the hemiacetal bond (between oxygen and C-1 on the pyran ring), followed by dehydration between the hydroxyl groups on the C2 and C5 positions.
XLR-11 was metabolized by phase I and II enzymes in human hepatocytes; more than 25 XLR-11 metabolites were produced by hydroxylation, carboxylation, hemiketal and hemiacetal formation, internal dehydration, and further glucuronidation of some oxidative metabolites.
Furthermore there was a possibility of unstable hemiacetal formation which does not contribute in the overall antiglycation effect of these molecules.
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