Document Type
Article
Publication Date
8-14-2015
Abstract
© The Royal Society of Chemistry. We describe a strategy to chlorinate stereocomplementary acyclic aliphatic 1,3-diols using a mixture of triphosgene and pyridine. While 1,3-anti diols readily led to 1,3-anti dichlorides, 1,3-syn diols must be converted to 1,3-syn diol monosilylethers to access the corresponding 1,3-syn dichlorides. These dichlorination protocols were operationally simple, very mild, and readily tolerated by advanced synthetic intermediates.
Publication Source (Journal or Book title)
Chemical Communications
First Page
15075
Last Page
15078
Recommended Citation
Villalpando, A., Saputra, M., Tugwell, T., & Kartika, R. (2015). Triphosgene-pyridine mediated stereoselective chlorination of acyclic aliphatic 1,3-diols. Chemical Communications, 51 (81), 15075-15078. https://doi.org/10.1039/c5cc06365e