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Synthesis 2014; 46(16): 2133-2142
DOI: 10.1055/s-0034-1378392
DOI: 10.1055/s-0034-1378392
feature article
Product Selectivity Control in the Domino Cyclization of 2-(2-Alkynylarylidene)-1,3-dicarbonyl Compounds Catalyzed by Metal Lewis Acids
Weitere Informationen
Publikationsverlauf
Received: 21. Mai 2014
Accepted after revision: 23. Juni 2014
Publikationsdatum:
08. Juli 2014 (online)

Abstract
The selective synthesis of different products from the same kind of starting materials is an attractive, but challenging, task for chemists. This article reports our design for the selective domino reactions of 2-(2-alkynylarylidene)-1,3-dicarbonyl compounds which can be prepared from o-alkynylbenzaldehyde and 1,3-dicarbonyl compounds. Several different types of polycyclic skeletons can be constructed from 2-(2-alkynylarylidene)-1,3-dicarbonyl compounds with by simple subtle modification of the structure or choice of reaction conditions.
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For selected examples, see:
For selected reviews and, see:
For selected reviews, see:
For recent selected examples on the cyclization of o-ethynylphenylalkenes, see:
For example on the cyclization of 2-(2-alkynylarylidene)malonates, see:
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