Facile organocatalytic domino oxidation of diols to lactones by in situ-generated TetMe-IBX
S Jhulki, S Seth, M Mondal, JN Moorthy
Index: Jhulki, Samik; Seth, Saona; Mondal, Manas; Moorthy, Jarugu Narasimha Tetrahedron, 2014 , vol. 70, # 13 p. 2286 - 2293
Full Text: HTML
Citation Number: 5
Abstract
Abstract The domino oxidation of diols to lactones is an important transformation, and catalytic protocols that allow this conversion smoothly are scarce. Capitalizing on the established reactivity of tetramethyl-IBX (TetMe-IBX) and its in situ generation in the presence of a co-oxidant, such as oxone, we have shown that a variety of diols can be converted to the corresponding lactones in respectable yields by employing the precursor ...
Related Articles:
[Ohta, Hiromichi; Tetsukawa, Hatsuki; Noto, Naoko Journal of Organic Chemistry, 1982 , vol. 47, # 12 p. 2400 - 2404]
[Tetrahedron Letters, , vol. 54, # 6 p. 515 - 517]
[Sodhi, Ravinderpal Kour; Paul, Satya; Clark Green Chemistry, 2012 , vol. 14, # 6 p. 1649 - 1656]
[Journal of the American Chemical Society, , vol. 132, # 2 p. 713 - 724]
[Yuan, Yu; Ji, Xiang; Zhao, Dongbo European Journal of Organic Chemistry, 2010 , # 27 p. 5274 - 5278]