Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones.
نویسندگان
چکیده
In the presence of an oxidant, sodium iodide is converted into hypoiodous acid which effects the rearrangement of tertiary propargylic alcohols to α-iodoenones in good yields.
منابع مشابه
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ورودعنوان ژورنال:
- Organic & biomolecular chemistry
دوره 10 43 شماره
صفحات -
تاریخ انتشار 2012