Synlett 2013; 24(13): 1657-1662
DOI: 10.1055/s-0033-1339298
letter
© Georg Thieme Verlag Stuttgart · New York

Tandem Hydroformylation–Biginelli Reaction

Daniela Fuchs
a   Institut für Organische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstrasse 21, 79104 Freiburg i. Bg., Germany   Fax: +49(761)2038715   Email: bernhard.breit@chemie.uni-freiburg.de
,
Mahboobeh Nasr-Esfahani
a   Institut für Organische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstrasse 21, 79104 Freiburg i. Bg., Germany   Fax: +49(761)2038715   Email: bernhard.breit@chemie.uni-freiburg.de
,
Lisa Diab
a   Institut für Organische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstrasse 21, 79104 Freiburg i. Bg., Germany   Fax: +49(761)2038715   Email: bernhard.breit@chemie.uni-freiburg.de
,
Tomáš Šmejkal
b   Syngenta Crop Protection AG, Schaffhauserstrasse, 4332 Stein, Switzerland
,
Bernhard Breit*
a   Institut für Organische Chemie, Albert-Ludwigs-Universität Freiburg, Albertstrasse 21, 79104 Freiburg i. Bg., Germany   Fax: +49(761)2038715   Email: bernhard.breit@chemie.uni-freiburg.de
› Author Affiliations
Further Information

Publication History

Received: 24 April 2013

Accepted after revision: 29 May 2013

Publication Date:
12 July 2013 (online)


Abstract

The combination of a tandem process with a multicomponent reaction is a new approach to high atom-economic synthesis. A tandem hydroformylation–Biginelli reaction sequence has been developed leading to a variety of functionalized 4-alkyl-substituted 3,4-dihydropyrimidin-2(1H)-ones.

Supporting Information

 
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