Issue 30, 2012

Efficient proline and prolinol ether mediated 3-component synthesis of 3- and 3,4-substituted chromenone derivatives

Abstract

A highly efficient route for the synthesis of valuable 3,4-substituted chromenone derivatives by the reaction of 1,3-diketones with aldehydes in the presence of L-proline was developed. The reactions take advantage of readily available starting materials and follow a Knoevenagel condensation/Michael addition/hemiacetalization domino process. Chiral 3-substituted chromenones are obtained with high enantioselectivities when a chiral diarylprolinol TMS-ether is applied in the reaction.

Graphical abstract: Efficient proline and prolinol ether mediated 3-component synthesis of 3- and 3,4-substituted chromenone derivatives

Supplementary files

Article information

Article type
Paper
Submitted
29 ፌብሩ 2012
Accepted
19 ኤፕሪ 2012
First published
14 ሜይ 2012

Org. Biomol. Chem., 2012,10, 6201-6210

Efficient proline and prolinol ether mediated 3-component synthesis of 3- and 3,4-substituted chromenone derivatives

M. Rueping, E. Merino and M. Bolte, Org. Biomol. Chem., 2012, 10, 6201 DOI: 10.1039/C2OB25443C

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