Issue 22, 1994

Carbonyl oxide chemistry. Part 3. Regioselectivity of the first [3 + 2] cycloaddition of carbonyl oxides to phenyl isocyanate: one-pot synthesis of 1,2,4-dioxazolidin-3-ones

Abstract

Carbonyl oxides 3 react with phenyl Isocyanate to give the 1, 2, 4-dioxazolidin-3-ones 4, providing a potentially useful synthesis of a heterocyclic system which is structurally related to several biologically active products. The crystal structure of the dioxazolidinone 4a is also reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 3295-3298

Carbonyl oxide chemistry. Part 3. Regioselectivity of the first [3 + 2] cycloaddition of carbonyl oxides to phenyl isocyanate: one-pot synthesis of 1,2,4-dioxazolidin-3-ones

M. R. Iesce, F. Cermola, F. Giordano, R. Scarpati and M. L. Graziano, J. Chem. Soc., Perkin Trans. 1, 1994, 3295 DOI: 10.1039/P19940003295

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