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Collect. Czech. Chem. Commun. 1996, 61, 1805-1814
https://doi.org/10.1135/cccc19961805

On the Stereoselectivity of the (-)-Dimenthyl Malonate Addition to α,β-Unsaturated Ketones

Ľubomír Šeboa, Juraj Alföldib, Grety Rihsc and Štefan Tomaa

a Department of Organic Chemistry, Comenius University, 842 15 Bratislava, Slovak Republic
b Institute of Chemistry, Slovak Academy of Sciences, 842 15 Bratislava, Slovak Republic
c CIBA-GEIGY Co., CH-4002 Basel, Switzerland

Crossref Cited-by Linking

  • SEBO L., ALFOELDI J., RIHS G., TOMA S.: ChemInform Abstract: Stereoselectivity of the (-)-Dimenthyl Malonate Addition to α,. beta.-Unsaturated Ketones. ChemInform 2010, 28, no. <https://doi.org/10.1002/chin.199720033>
  • Kim Sung-Ji, Lee Kyoungyim, Jew Sang-sup, Park Hyeung-geun, Jeong Byeong-Seon: C2-Symmetric Chiral Malonamides for Asymmetric Michael Reaction. Chem. Lett. 2008, 37, 432. <https://doi.org/10.1246/cl.2008.432>
  • Dolmella A., Gatto S., Girardi E., Bandoli G.: X-ray structures of the anticoagulants coumatetralyl and chlorophacinone. Theoretical calculations and SAR investigations on thirteen anticoagulant rodenticides. Journal of Molecular Structure 1999, 513, 177. <https://doi.org/10.1016/S0022-2860(99)00119-2>