A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane
A general strategy for fast decarboxylative difunctionalization to gem-dihalohydrin, gem-dihaloether, gem-dibromoester and cyclized bromo-1,4-dioxane synthons with outstanding regio- and stereoselectivity is demonstrated. The Royal Society of Chemistry 20
Khamarui, Saikat,Sarkar, Deblina,Pandit, Palash,Maiti, Dilip K.
supporting information; experimental part
p. 12667 - 12669
(2012/01/03)
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