A one pot synthesis of 5-phenyl-1,3-dioxane-4,6-dione derivatives

Article abstract of DOI:10.1080/00397910008086875

A general procedure for synthesis of 5-phenyl-1,3-dioxane-4,6-dione derivatives is described. The synthesis involves the cycloaddition of (α- chlorocarbonyl)phenylketene with carbonyl compounds to generate the corresponding substituted 2-oxetanone's which is readily transformed to the final products in one step. The 1,3-dioxane-4,6-dione is a rigid cyclic structure, and can undergo easy hydrolysis.

Full text of DOI:10.1080/00397910008086875

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Synthetic Communications: An
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Organic Chemistry
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A One Pot Synthesis of 5-
Phenyl-1,3-Dioxane-4,6-Dione
Derivatives
K. Saidi a , H. R. Shaterian a & H. Sheibani a
a Department of Chemistry, Shahid Bahonar
University of Kerman, Kerman, 76175, Iran
Published online: 04 Dec 2007.
To cite this article: K. Saidi , H. R. Shaterian & H. Sheibani (2000) A One Pot
Synthesis of 5-Phenyl-1,3-Dioxane-4,6-Dione Derivatives, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
30:13, 2345-2351, DOI: 10.1080/00397910008086875
To link to this article: http://dx.doi.org/10.1080/00397910008086875
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