The selective conversion of 1-(2-furyl)-2-hydroxyethan-1-one and ethyl 2-(2-furyl)-2-oxo acetate into (E)-and (Z)oximes and oxime ethers followed by oxazaborolidine-catalyzed enantioselective reduction using different amino alcohols furnished both enantiomers of the important chiral building block 2
β¦ LIBER β¦
Synthesis of a 2-hydroxymethyl-dihydropyridone-system as a flexible building block for the preparation of azasugars
β Scribed by Hans-Josef Altenbach; Ralf Wischnat
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 121 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
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