Wolfrom et al., 1946 - Google Patents
N-Methyl-L-glucosaminic Acid1Wolfrom et al., 1946
- Document ID
- 1555343226706408278
- Author
- Wolfrom M
- Thompson A
- Hooper I
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
N-Methyl-L-glucosaminic Acid1 Page 1 Nov., 1946 N-Methyl-l-glucosaminic Acid 2343
Experimental d,L-Glucitol (and its Hexaacetate) from Product B.— In a plant electroreduction of
D-glucose at pH 10-13 and below 30 (resultant material designated product B) a crystalline …
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 OCC(O)C(O)C(O)C(O)CO 0 abstract description 7
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- C07H15/14—Acyclic radicals, not substituted by cyclic structures attached to a sulfur, selenium or tellurium atom of a saccharide radical
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- C—CHEMISTRY; METALLURGY
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- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07C255/00—Carboxylic acid nitriles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/38—Separation; Purification; Stabilisation; Use of additives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
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