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Sugar molecule with an –OH group at the end(s) of the carbon chain
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group at the terminal end of an aldose or ketose is oxidized.
413:
Davies
Michael B.; Austin John; Partridge David A. (1991).
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417:. The Royal Society of Chemistry. p. 48.
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443:at the U.S. National Library of Medicine
415:Vitamin C: Its Chemistry and Biochemistry
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57:Main classes of sugar acids include:
389:Essentials of carbohydrate chemistry
164:3-Deoxy-D-manno-oct-2-ulosonic acid
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202:Examples of sugar acids include:
162:An ulosonic acid; specifically,
50:at one end or both ends of its
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72:) located at the initial end (
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138:) of an aldose are oxidized.
98:) at the initial end of a 2-
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102:is oxidized creating an α-
265:Ketodeoxyoctulosonic acid
230:(6C, unsaturated lactone)
445:Medical Subject Headings
392:. New York: Springer.
366:
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126:, in which both ends (
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277:-oct-2-ulosonic acid)
261:-non-2-ulosonic acid)
241:(5-amino-3,5-dideoxy-
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386:Robyt, J.F. (1998).
88:hydroxymethyl group
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317:-Galactaric acid (
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292:Galacturonic acid
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32:organic chemistry
16:(Redirected from
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362:The β-D form of
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327:-Glucaric acid (
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267:(KDO or 3-deoxy-
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364:glucuronic acid
286:Glucuronic acid
239:Neuraminic acid
235:Ulosonic acids
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112:, in which the
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84:Ulosonic acids
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66:aldehyde group
48:carboxyl group
44:monosaccharide
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346:Ascorbic acid
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309:Tartaric acid
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298:Iduronic acid
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282:Uronic acids
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228:Ascorbic acid
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210:Glyceric acid
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216:Xylonic acid
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188:Aldaric acid
151:Aldonic acid
110:Uronic acids
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80:is oxidized.
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40:acidic sugar
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461:Sugar acids
441:Sugar+Acids
176:Uronic acid
18:Sugar acids
374:References
319:Mucic acid
74:position 1
36:sugar acid
350:Vitamin C
455:Category
198:Examples
104:ketoacid
76:) of an
258:galacto
248:glycero
46:with a
447:(MeSH)
421:
396:
331:) (6C)
321:) (6C)
100:ketose
78:aldose
274:manno
128:−CH=O
70:−CH=O
52:chain
42:is a
419:ISBN
394:ISBN
315:meso
311:(4C)
300:(6C)
294:(6C)
288:(6C)
224:(6C)
218:(5C)
212:(3C)
130:and
34:, a
132:−CH
114:−CH
92:−CH
38:or
30:In
457::
136:OH
118:OH
96:OH
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271:-
269:D
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253:D
251:-
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243:D
134:2
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90:(
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