Stereoselective Transformations Leading to Pentono-1,4-Lactones1
Authors:
- 1 November 1996
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 15 (8) , 975-984
Abstract
The readily available 2, 3-O-isopropylidene-D-erythrose has been stereoselectively transformed into L-ribono and D/L lyxonolactone derivatives via dihydroxylation, iodolactonisation and epoxidation. Also D-ribono-1,4-lactone was converted into L-lyxono-1,4-lactone. These lactones are considered as important starting materials for the synthesis of several chiral compounds. Our observations during these transformations are also presented.Keywords
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