1,5-Anhydro- d-fructose from d-fructose

1,5-Anhydro- d-fructose was efficiently prepared from d-fructose via regiospecific 1,5-anhydro ring formation of 2,3- O-isopropylidene-1- O-methyl(tolyl)sulfonyl- d-fructopyranose and subsequent deprotection.

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Bibliographic Details
Published inCarbohydrate research Vol. 342; no. 9; pp. 1249 - 1253
Main Authors Dekany, Gyula, Lundt, Inge, Niedermair, Fabian, Bichler, Sabine, Spreitz, Josef, (Fitz) Sprenger, Friedrich K., Stütz, Arnold E.
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 02.07.2007
Elsevier
Subjects
1,5-Anhydro- d-fructose
Biochemistry & Molecular Biology
Carbohydrate Conformation
Chemistry
Chemistry, Applied
Chemistry, Organic
Fructose - analogs & derivatives
Fructose - chemical synthesis
Fructose - chemistry
Life Sciences & Biomedicine
Models, Chemical
Molecular Structure
Physical Sciences
Science & Technology
Synthesis
1,5-Anhydro- d-fructose
Synthesis
synthesis
ACID
1,5-ANHYDROGLUCITOL
UNSATURATED ANHYDRO-SUGAR
1,5-ANHYDROFRUCTOSE
1,5-anhydro-D-fructose
DERIVATIVES
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Summary:1,5-Anhydro- d-fructose was efficiently prepared from d-fructose via regiospecific 1,5-anhydro ring formation of 2,3- O-isopropylidene-1- O-methyl(tolyl)sulfonyl- d-fructopyranose and subsequent deprotection.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:0008-6215
1873-426X
DOI:10.1016/j.carres.2007.02.026