Author
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Price, Neil |
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Sheng, Suzie |
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Submitted to: Meeting Abstract
Publication Type: Abstract Only Publication Acceptance Date: 10/1/2005 Publication Date: 10/10/2005 Citation: Price, N.P., Sheng, S.S. 2005. Functionalized beta-c-glycosidic ketone hydrazones: novel derivatives for carbohydrate analysis by maldi-tof mass spectrometry [abstract]. Annual Midwest Carbohydrate Meeting. Poster #4. Interpretive Summary: Technical Abstract: Hydrazones constitute one of the best derivatives for the analysis of aldehydes and ketones yielding crystalline solids that are readily precipitated from water. Unlike simple aldehydes and ketones, sugars do not usually form simple hydrazones. They react with three equivalents of aryl- or acylhydrazines at both the C1 and C2 carbons to give sugar osazones. The first equivalent forms an imine with the aldehyde or ketone group. The second equivalent oxidizes the alcohol adjacent to the first imine to a carbonyl group. The newly formed carbonyl then reacts with a third equivalent of the hydrazone to give an osazone. Since the reaction is at C1 and C2, a ketose will therefore give the same osazone as the related aldose. For the same reason C2-epimers, such as glucose and mannose, also give rise to identical osazones. This well known reaction has therefore tended to limit the usefulness of hydrazones for the analysis of sugars. Here we show the potential of new carbohydrate-based derivatives, beta-C-glycosidic ketones, for the formation of various functionalized hydrazones. |
