29887-56-7Relevant articles and documents
Trans dialkoxylation of cyclic alkenes: A Prevost-type reaction
Schauble, J. Herman,Trauffer, Edward A.,Deshpande, Prashant P.,Evans, Robert D.
, p. 1333 - 1339 (2007/10/03)
Reaction of anhydrous silver perchlorate, sym-collidine, and iodine (2:1:1 molar ratio) with cyclic alkenes and an excess of an alcohol in CH 2Cl2 affords trans-1,2-dialkoxycycloalkanes in high yields and purity. The reaction occurs via initial formation of the trans-iodoethers, which undergo Ag-assisted iodide abstraction to give the trans-diethers. Georg Thieme Verlag Stuttgart.
Oxone Oxidation of Selenides: A Mild and Efficient Method for the Preparation of Selenones
Ceccherelli, Paolo,Curini, Massimo,Epifano, Francesco,Marcotullio, Maria Carla,Rosati, Ornelio
, p. 8412 - 8413 (2007/10/02)
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