Iodine(III)-mediated halogenations of acyclic monoterpenoids
作者:Laure Peilleron、Tatyana D Grayfer、Joëlle Dubois、Robert H Dodd、Kevin Cariou
DOI:10.3762/bjoc.14.96
日期:——
Five different halofunctionalizations of acyclic monoterpenoids were performed using a combination of a hypervalent iodine(III) reagent and a halide salt. In this manner, the dibromination, the bromo(trifluoro)acetoxylation, the bromohydroxylation, the iodo(trifluoro)acetoxylation or the ene-type chlorination of the distal trisubstituted double bond occurred with excellent selectivity and moderate