Journal
ORGANIC LETTERS
Volume 9, Issue 2, Pages 367-370Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol062939g
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Cyclic enesulfonamides, enecarbamates, or enamides tethered to an alkyne cyclize readily with use of platinum(II) chloride. This reaction generates quaternary-substituted carbon centers within simple spiro-fused or more complex tri- and tetracyclic heterocyclic ring systems. The yields for this process range from 50% to 83%.
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