## Abstract 2‐Deoxy‐D‐ribose (1) was converted into its methyl glycofuranoside 2, which was treated with 4‐biphenylcarbonyl chloride to give a separable mixture of 3 (26%) and 4 (40%). Compounds 3 and 4 were deoxygenated by Barton deoxygenation to give the corresponding 2,3‐dideoxyribose derivative
ChemInform Abstract: A New Route to 2,2′,3,3′-Tetrasubstituted Binaphthyls.
✍ Scribed by Michael Widhalm; Christian Aichinger; Kurt Mereiter
- Publisher
- John Wiley and Sons
- Year
- 2009
- Weight
- 31 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0931-7597
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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 “Full Text” option. The original article is trackable v
New Routes to Benzothiophenes, Isothiazoles and 1,2,3-Dithiazoles. -New and clean conversions of the dithiazolethione (I) into highly functionalized isothiazoles (V), (VI) and benzothiophene (IX) are described. Plausible mechanisms are proposed for all of these reactions. -(EMAYAN, K.;