19739-09-4Relevant academic research and scientific papers
Bromination of alkenes and alkynes with (bromodimethyl)sulfonium bromide
Das, Biswanath,Srinivas, Yallamalla,Sudhakar, Chittaluri,Ravikanth, Bommena
, p. 188 - 190 (2008)
Alkenes and alkynes were brominated efficiently in high yields with (bromodimethyl)sulfonium bromide in acetonitrile at room temperature. Alkenes produced the corresponding trans-dibromo compounds while alkynes (except phenylacetylene) afforded both the trans-dibromo products (major) and the tetrabromo derivatives (minor). However, phenylacetylene furnished solely the tetrabromo compound.
Efficient bromination of alkenes and alkynes using potassium bromide and diacetoxy iodobenzene
Das, Biswanath,Srinivas, Yallamalla,Sudhakar, Chittaluri,Damodar, Kongara,Narender, Ravirala
experimental part, p. 220 - 227 (2009/04/07)
Bromination of alkenes and alkynes has efficiently been carried out at room temperature in short reaction times using KBr and diacetoxy iodobenzene in CH2Cl2-H2O (1:1) to prepare the corresponding trans-dibromo compounds in excellent yields. Copyright Taylor & Francis Group, LLC.
