Ozonolytic cleavage of cycloalkenes to terminally differentiated products
SL Schreiber, RE Claus, J Reagan
Index: Schreiber, Stuart L.; Claus, Ronald E.; Reagan, Jeff Tetrahedron Letters, 1982 , vol. 23, # 38 p. 3867 - 3870
Full Text: HTML
Citation Number: 208
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Conditions are reported which convert cycloalkenes to terminally differentiated products through the intermediacy of α-alkoxy hydroperoxides. ... In a typical experiment, 10% pTSOH (w/w) is added after ozonolysis and the reaction mixture is stirred for 1.5 hr at RT to assure ...
Related Articles:
[Fujioka, Hiromichi; Okitsu, Takashi; Sawama, Yoshinari; Murata, Nobutaka; Li, Ruichuan; Kita, Yasuyuki Journal of the American Chemical Society, 2006 , vol. 128, # 17 p. 5930 - 5938]
[Cryle, Max J.; Ortiz De Montellano, Paul R.; De Voss, James J. Journal of Organic Chemistry, 2005 , vol. 70, # 7 p. 2455 - 2469]
[Fujioka, Hiromichi; Okitsu, Takashi; Sawama, Yoshinari; Murata, Nobutaka; Li, Ruichuan; Kita, Yasuyuki Journal of the American Chemical Society, 2006 , vol. 128, # 17 p. 5930 - 5938]
[Fuchs, Daniela; Rousseau, Geraldine; Diab, Lisa; Gellrich, Urs; Breit, Bernhard Angewandte Chemie - International Edition, 2012 , vol. 51, # 9 p. 2178 - 2182]