Synthesis of a 2,3-dideoxy-2,3-difluorofuranose with the D-lyxo configuration. An intramolecular rearrangement of methyl 5-O-benzoyl-2,3-dideoxy-2,3-difluoro-D-lyxofuranoside observed during the attempted synthesis of 1-(2,3-dideoxy-2,3-difluoro-beta-D-lyxofuranosyl)thymine.

Jeong, L S; Lim, B B; Marquez, V E

Jeong, L S; Lim, B B; Marquez, V E.

Affiliation

Jeong LS; Laboratory of Medicinal Chemistry, National Cancer Institute, NIH, Bethesda, MD 20892.

Carbohydr Res ; 262(1): 103-14, 1994 Sep 01.

Article in En | MEDLINE | ID: mdl-7954518

Subject(s)

Deoxy Sugars/chemistry; Glycosides/chemistry; Thymidine/analogs & derivatives; Carbohydrate Conformation; Molecular Structure; Thymidine/chemical synthesis

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Collection: 01-internacional Database: MEDLINE Main subject: Thymidine / Deoxy Sugars / Glycosides Language: En Journal: Carbohydr Res Year: 1994 Document type: Article

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Collection: 01-internacional Database: MEDLINE Main subject: Thymidine / Deoxy Sugars / Glycosides Language: En Journal: Carbohydr Res Year: 1994 Document type: Article