117895-47-3Relevant articles and documents
Convergent access to bis-spiroacetals through a sila-Stetter-ketalization cascade
Labarre-Laine, Jessica,Beniazza, Redouane,Desvergnes, Valerie,Landais, Yannick
supporting information, p. 4706 - 4709 (2013/10/08)
An NHC-catalyzed sila-Stetter reaction between aliphatic acylsilanes and vinylketones bearing silyl ether substituents affords functionalized 1,4-diketones, which upon treatment under acidic conditions leads to the corresponding bis-spiroacetals. The two-step sequence may also be carried out in a one-pot operation leading to high yields of the desired bis-spiroacetals.
An aldol-based synthesis of(+)-peloruside a, a potent microtubule Stabilizing Agent
Evans, David A.,Welch, Dennie S.,Speed, Alexander W. H.,Moniz, George A.,Reichelt, Andreas,Ho, Stephen
supporting information; experimental part, p. 3840 - 3841 (2009/08/08)
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Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes
Suzuki, Masaki,Tomooka, Katsuhiko
, p. 651 - 654 (2007/10/03)
The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.