γ-Keto Esters and γ-Butyrolactones from the Reaction of Dialkoxydihydrofurans with Trimethylsilyl Iodide
BL Feringa, W Dannenberg
Index: Feringa, Ben L.; Dannenberg, W. Synthetic Communications, 1983 , vol. 13, # 6 p. 509 - 514
Full Text: HTML
Citation Number: 10
Abstract
Abstract: Dimethoxydihydrofurans are converted into Y-keto e,sters and 7-butyrolactones by a new procedure using an equimolar quantity and an excess of trimethylsilyl iodide, respectively. ... The synthesis of 1,4-dicarbonyl compounds, useful precursors ... The recent report by Suzuki and co-workers2 on the conversion of ... Applications of TMSI as a Lewis acid catalyst and as a reagent ... Unexpectedly, however, when we used TMSI in .the ...
Related Articles:
[Banwell, Martin G.; Edwards, Alison J.; Jolliffe, Katrina A.; Smith, Jason A.; Hamel, Ernest; Verdier-Pinard, Pascal Organic and Biomolecular Chemistry, 2003 , vol. 1, # 2 p. 296 - 305]
[Dyer, Philip W.; Fawcett, John; Hanton, Martin J. Journal of Organometallic Chemistry, 2005 , vol. 690, # 23 p. 5264 - 5281]
[Kawashima, Masatoshi; Sato, Toshio; Fujisawa, Tamotsu Bulletin of the Chemical Society of Japan, 1988 , vol. 61, p. 3255 - 3264]
[Kawashima, Masatoshi; Fujisawa, Tamotsu Chemistry Letters, 1984 , p. 1851 - 1854]
[Kawashima, Masatoshi; Sato, Toshio; Fujisawa, Tamotsu Bulletin of the Chemical Society of Japan, 1988 , vol. 61, p. 3255 - 3264]