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Solvent-dependent, rhodium catalysed rearrangement reactions of sulfur ylides
Zhen Yang1, Yujing Guo1, Rene M Koenigs1
1RWTH Aachen University, Institute of Organic Chemistry, Landoltweg, D-52074 Aachen, Germany. rene.koenigs@rwth-aachen.de.
Abstract:
Benzyl thioethers undergo rhodium(ii) catalyzed sigmatropic rearrangement reactions with aryldiazoacetates. Depending on the solvent and the electronic properties of the sulfide, the intermediate ylide undergoes either [1,2]- or [2,3]-sigmatropic rearrangement reactions in high yields.
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