Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5282067 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
1,2-O-Isopropylidene-α-l-glucurono-3,6-lactone may be synthesized on a 100-200 g scale from cheaply available d-glucoheptonolactone in an overall yield of 94% in four steps via l-glucuronolactone. Subsequent elaboration to l-glucose, diacetone-l-glucose (1,2:5,6-di-O-isopropylidene-α-l-glucofuranose), and monoacetone-l-glucose (1,2-O-isopropylidene-α-l-glucofuranose) allows easy access to a range of l-sugar chirons.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alexander C. Weymouth-Wilson, Robert A. Clarkson, Nigel A. Jones, Daniel Best, Francis X. Wilson, Maria-Soledad Pino-González, George W.J. Fleet,