Stereoselective transformations leading to pentono -1, 4-lactones

Article abstract of DOI:10.1080/07328309608005703

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,

Full text of DOI:10.1080/07328309608005703

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Journal of Carbohydrate Chemistry
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Stereoselective Transformations Leading
to Pentono-1,4-Lactones
B. Venkateswara Rao a & Saswata Lahiri a
a Organic III, Indian Institute of Chemical Technology , Hyderabad,
500 007, India
Published online: 19 Aug 2006.
To cite this article: B. Venkateswara Rao & Saswata Lahiri (1996) Stereoselective Transformations
Leading to Pentono-1,4-Lactones , Journal of Carbohydrate Chemistry, 15:8, 975-984, DOI:
10.1080/07328309608005703
To link to this article: http://dx.doi.org/10.1080/07328309608005703
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