98381-89-6Relevant academic research and scientific papers
Peroxide promoted tunable decarboxylative alkylation of cinnamic acids to form alkenes or ketones under metal-free conditions
Ji, Jing,Liu, Ping,Sun, Peipei
supporting information, p. 7546 - 7549 (2015/05/04)
A tunable decarboxylative alkylation of cinnamic acids with alkanes was developed to form alkenes or ketones under transition metal-free conditions. In the presence of DTBP or DTBP/TBHP, the reaction gave alkenes and ketones respectively via a radical mechanism in moderate to good yields. This journal is
Copper catalyzed direct alkenylation of simple alkanes with styrenes
Zhu, Yefeng,Wei, Yunyang
, p. 2379 - 2382 (2014/05/20)
A novel Cu-catalyzed direct alkenylation of simple alkanes with styrenes was described. In the presence of a catalytic amount of Cu(OTf)2, a diverse range of alkenes undergo coupling with cycloalkanes to produce (E)-alkyl alkenes. This transformation is proposed to proceed via a radical process. This journal is the Partner Organisations 2014.
REACTION OF ALKYL BROMIDES WITH STYRENE IN THE PRESENCE OF A NICKEL CATALYST
Lebedev, S. A.,Lopatina, V. S.,Luk'yanova, T. V.,Berestova, S. S.,Shifrina, R. R.,et al.
, p. 652 - 656 (2007/10/02)
Alkyl bromides enter into reaction with styrene in the presence of a nickel catalyst to form the products from substitution of the vinyl hydrogen of styrene, i.e., E-1-phenyl-1-alkenes.A high yield of E-1-phenyl-1-alkenes is promoted by the use of seconda
