Smith, 1946 - Google Patents
Analogs of ascorbic acidSmith, 1946
- Document ID
- 4883273484980365495
- Author
- Smith F
- Publication year
- Publication venue
- Advances in Carbohydrate Chemistry
External Links
Snippet
Publisher Summary This chapter discusses the synthesis of the analogs of ascorbic acid. The unique feature of L-ascorbic acid and its analogs lies in the enediolic system, and it is this system that is responsible for the remarkable reducing properties displayed by these …
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 OC[C@H](O)[C@H]1OC(=O)C(O)=C1O 0 title abstract description 103
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester
- C07C67/42—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester by oxidation of secondary alcohols or ketones
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