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Pure Appl. Chem., 1997, Vol. 69, No. 3, pp. 605-608

http://dx.doi.org/10.1351/pac199769030605

Application of enolates of activated carboxylic acid derivatives in organic synthesisnovel syntheses of β-lactones

C. Wedler, Ralf Ludwig and H. Schick

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  • Mitchell T. Andrew, Vallakati Ravikrishna, Pérez Lisa M., Romo Daniel, Zhao Cunxiang: Mechanistic Investigations of the ZnCl2-Mediated Tandem Mukaiyama Aldol Lactonization: Evidence for Asynchronous, Concerted Transition States and Discovery of 2-Oxopyridyl Ketene Acetal Variants. S J Am Chem Soc 2012, 134, 3084. <http://dx.doi.org/10.1021/ja209163w>
  • WEDLER C., LUDWIG R., SCHICK H.: ChemInform Abstract: Application of Enolates of Activated Carboxylic Acid Derivatives in Organic Synthesis - Novel Syntheses of β-Lactones. ChemInform 2010, 28, no. <http://dx.doi.org/10.1002/chin.199728249>
  • Yang Hong Woon, Romo Daniel: Methods for the synthesis of optically active β-lactones (2-oxetanones). Tetrahedron 1999, 55, 6403. <http://dx.doi.org/10.1016/S0040-4020(99)00185-4>
  • Nelson Scott G., Peelen Timothy J., Wan Zhonghui: Mechanistic alternatives in Lewis acid-catalyzed acyl halidealdehyde cyclocondensations. Tetrahetron Lett 1999, 40, 6541. <http://dx.doi.org/10.1016/S0040-4039(99)01309-X>