Asymmetric chemical oxidations of aryl and alkyl 2-(trimethylsilyl)ethyl sulfides

DOI: 10.1016/0957-4166(94)00368-L

Source and publish data:

Tetrahedron Asymmetry p. 131 - 138 (1995)

Update date:2022-08-16

Topics:

Authors:

Schwan Schwan

Pippert Pippert

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Article abstract of DOI:10.1016/0957-4166(94)00368-L

A collection of aryl and alkyl 2-(trimethylsilyl)methyl sulfides have been converted to their respective sulfoxides by four different asymmetric oxidizing agents. The chemical yields range from 44-98% while the enantiomeric excesses range from 0-89%. The

Full text of DOI:10.1016/0957-4166(94)00368-L

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