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Synlett 2003(8): 1101-1104
DOI: 10.1055/s-2003-39904
DOI: 10.1055/s-2003-39904
LETTER
© Georg Thieme Verlag Stuttgart ˙ New YorkEfficient Synthesis of Highly Functionalized Triquinane Derivatives through Dicobalt Octacarbonyl-Catalyzed Cycloaddition of Diyne with Diene under Carbon Monoxide Followed by Cleavage of a Double Bond
Weitere Informationen
Received
9 April 2003
Publikationsdatum:
11. Juni 2003 (online)
Publikationsverlauf
Publikationsdatum:
11. Juni 2003 (online)

Abstract
A new approach to the synthesis of angular triquinanes, based on the dicobalt octacarbonyl-catalyzed tandem cycloaddition of diyne and diene followed by cleavage of a double bond, is described.
Key word
transition metal catalysis - tandem cyclo-addition - angular triquinane - dicobalt octacarbonyl
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