4.7 Article

First examples of proline-catalyzed domino Knoevenagel/hetero-Diels-Alder/elimination reactions

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ADVANCED SYNTHESIS & CATALYSIS
卷 347, 期 10, 页码 1353-1355

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200505144

关键词

domino reaction; lactones; Meldrum's acid; organocatalysis

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A novel and efficient one-pot synthesis of lactones (pyranones) has been achieved by domino Knoevenagel/hetero-Diels-Alder/elimination reactions of O- and N-prenyl aldehyde derivatives with Meldrum's acid in the presence Of (L)- or (D),(L)-proline. The reaction proceeds cleanly at room temperature to afford cis- or trans-fused products in good yields with high diastereoselectivity.

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