Oxidation of thiols to disulfides with molecular bromine on hydrated silica gel support
Abstract
Results of oxidation of thiols to disulfides with molecular bromine on silica gel solid support are reported. The procedure utilizes organic media and does not require a base to neutralize HBr by-products to suppress acid promoted side reactions. Utilization of silica gel support simplifies work up and product isolation. © 2002 Elsevier Science Ltd. All rights reserved.
Publication Title
Tetrahedron Letters
Recommended Citation
Ali, M., & McDermott, M. (2002). Oxidation of thiols to disulfides with molecular bromine on hydrated silica gel support. Tetrahedron Letters (35), 6271-6273. https://doi.org/10.1016/S0040-4039(02)01220-0
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