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Synlett 1992; 1992(12): 985-987
DOI: 10.1055/s-1992-21556
DOI: 10.1055/s-1992-21556
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© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Vinylsulfonyl Chloride, a Ketene Equivalent for the Intramolecular Diels-Alder Reaction
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Publikationsdatum:
08. März 2002 (online)
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A completely regioselective and highly diastereoselective formal [4+2]-cycloaddition of ketene to 1,3-dienes bearing hydroxylated side chains is achieved by intramolecular Diels-Alder reaction of their vinylsulfonates followed by oxidative desulfurization.