5468-05-3Relevant articles and documents
Iodine-catalyzed tandem synthesis of terminal acetals and glycol mono esters from olefins
Kumar, Macharla Arun,Swamy, Peraka,Naresh, Mameda,Reddy, Marri Mahender,Rohitha, Chozhiyath Nappunni,Prabhakar, Sripadi,Sarma, Akella Venkata Subrahmanya,Kumar, Joseph Richard Prem,Narender, Nama
supporting information, p. 1711 - 1713 (2013/03/14)
A new metal-free protocol is described for the synthesis of terminal acetals by tandem oxidative rearrangement of olefins using oxone as an oxidant in the presence of iodine. Moreover, a one-pot procedure for the preparation of glycol mono esters from olefins is also presented for the first time using the same reagent system. The Royal Society of Chemistry 2013.
Acetals by AlFe-pillared montmorillonite catalysis
Cramarossa, Maria Rita,Forti, Luca,Ghelfi, Franco
, p. 15889 - 15894 (2007/10/03)
AlFe-pillared montmorillonite is an efficient catalyst for acetals preparation in CH2Cl2 at room temperature.