Document Type

Article

Publication Date

1-2015

Publication Title

Synthesis

Abstract

The (3+2)-cycloaddition reaction involving oxyallyl cations has proven to be a versatile and efficient approach for the construction of five-membered carbo- and heterocycles, which are prevalent frameworks in natural products and pharmaceuticals. The following article will provide a brief summary of recent disclosures on this process featuring chemo-, regio- and diastereoselective oxyallyl cycloadditions with both electron-rich and electron-deficient 2π partners.

DOI

10.1055/s-0034-1378918

Included in

Chemistry Commons

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