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Synthesis 2002(2): 0217-0220
DOI: 10.1055/s-2002-19810
DOI: 10.1055/s-2002-19810
PAPER
© Georg Thieme Verlag Stuttgart · New York
A Facile Synthesis of trans-Fused Pyrano[3,2-c]benzopyrans Catalyzed by Scandium Triflate
Weitere Informationen
Received
1 September 2001
Publikationsdatum:
03. August 2004 (online)
Publikationsverlauf
Publikationsdatum:
03. August 2004 (online)
Abstract
Scandium triflate has been utilized as an efficient Lewis acid for the intramolecular cycloaddition of o-quinonemethides (generated in situ from salicylaldehydes and unsaturated alcohols) to afford the corresponding trans-fused pyranobenzopyrans in high yields with high selectivity.
Key words
scandium triflate - o-quinonemethides - hetero Diels-Alder reaction - pyranobenzopyrans
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