Study of the Michael addition of β-cyclodextrin–thiol complexes to conjugated alkenes in water
Literature Information
N. Srilakshmi Krishnaveni, K. Surendra, K. Rama Rao
An environmentally benign and highly efficient supramolecular Michael addition of thiols from the secondary side of β-cyclodextrin to α,β-unsaturated compounds at the primary side in water is described in quantitative yields; products of undesirable side reactions resulting from polymerization are not observed; the use of cyclodextrin precludes the use of either acid or base and the catalyst can be recovered and reused.
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