The synthesis of a new bench stable and odourless zinc thiolate is here reported. The thiolysis of epoxides effected using this reagent showed a considerable rate acceleration when effected in “on water” conditions. In addition the reactions evidenced a good regioselectivity combining the advantage of the procedures effected in organic solvent with those effected using Lewis acid’s catalysis.

"On water” thiolysis of epoxides promoted by PhSZnBr

BAGNOLI, Luana;MARINI, Francesca;TESTAFERRI, Lorenzo;SANTI, Claudio
2013

Abstract

The synthesis of a new bench stable and odourless zinc thiolate is here reported. The thiolysis of epoxides effected using this reagent showed a considerable rate acceleration when effected in “on water” conditions. In addition the reactions evidenced a good regioselectivity combining the advantage of the procedures effected in organic solvent with those effected using Lewis acid’s catalysis.
2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1154872
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