Synthesis of 3,5-O-benzylidene-2-deoxy-L-riboaldose from 5,5-dihydroxy- 2-phenyl-1,3-dioxane

Article abstract of DOI:10.1080/00397910008086866

The asymmetric alkylation of 2-phenyl-1,3-dioxan-5-one was achieved via the RAMP-hydrazone. Regeneration of the ketone followed by stereoselective reduction and ozonolysis, gave the protected 2-deoxy-L-ribose, 3,5-O- benzyldiene-2-deoxy-L-erythro-pentoald

Full text of DOI:10.1080/00397910008086866

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of 3,5-O-
Benzylidene-2-deoxy-
L-riboaldose from 5,5-
Dihydroxy-2-phenyl-1,3-
dioxane
Trond Ulven a & Per H. J. Carlsen a
a Department of Organic Chemistry , Norwegian
University of Science and Technology , N-7034,
Trondheim, Norway
Published online: 04 Dec 2007.
To cite this article: Trond Ulven & Per H. J. Carlsen (2000) Synthesis of 3,5-O-
Benzylidene-2-deoxy-L-riboaldose from 5,5-Dihydroxy-2-phenyl-1,3-dioxane, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 30:13, 2275-2280, DOI: 10.1080/00397910008086866
To link to this article: http://dx.doi.org/10.1080/00397910008086866
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