摘要
Here we report the utilization of NH-sulfamoyl fluorides (RNHSO2F) as reliable SuFEx synthons for the construction of various sulfamate esters. By using potassium fluoride as base, we are able to convert RNHSO2F to azasulfene intermediates under mild conditions and guarantee their further efficent ligation with phenols and alcohols.
危险品化学品经营许可证（带存储）