Rapid synthesis of 5-O-(tert-butyldiphenylsilyl)-2-deoxy-L-ribonolactone

Article abstract of DOI:10.1080/00397919408010201

A convenient, four-step synthesis of the title compound (1) in 21% overall yield from L-arabinose is described. Selective formation of the 2-O-phenoxythiocarbonyl derivative 6 and its tributyltin hydride/azobis(isobutyronitrile) deoxygenation performed in

Full text of DOI:10.1080/00397919408010201

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Rapid Synthesis of 5-O-(tert-
Butyldiphenylsilyl)-2-deoxy-L-
ribonolactone
Rajiv Sharma a & Victor E. Marquez a
a Laboratory of Medicinal Chemistry, Developmental
Therapeutics Program, Division of Cancer
Treatment , National Cancer Institute NIH ,
Bethesda, Maryland, 20892, USA
Published online: 23 Sep 2006.
To cite this article: Rajiv Sharma & Victor E. Marquez (1994) Rapid Synthesis of 5-
O-(tert-Butyldiphenylsilyl)-2-deoxy-L-ribonolactone, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 24:13,
1937-1945, DOI: 10.1080/00397919408010201
To link to this article: http://dx.doi.org/10.1080/00397919408010201
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