Collect. Czech. Chem. Commun.
2002, 67, 353-364
https://doi.org/10.1135/cccc20020353
π-Facial Selectivity in 1,3-Dipolar Cycloaddition Reactions of α-Methylidene-γ-lactone Substituted by 4-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-1-yl Group in γ-Position
Petr Melša and Ctibor Mazal*
Department of Organic Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
Crossref Cited-by Linking
- Krajewska Urszula, Janecka Anna, Studzian Kazimierz, Janecki Tomasz, Albrecht Anna, Koszuk Jacek F., Modranka Jakub, Różalski Marek: Synthesis and cytotoxic activity of γ-aryl substituted α-alkylidene-γ-lactones and α-alkylidene-γ-lactams. biorg med chem 2008, 16, 4872. <https://doi.org/10.1016/j.bmc.2008.03.035>
- Melša Petr, Čajan Michal, Havlas Zdeněk, Mazal Ctibor: Substituent Effect on exo Stereoselectivity in the 1,3-Dipolar Cycloaddition Reaction of Tulipalin A with Nitrile Ylides. J. Org. Chem. 2008, 73, 3032. <https://doi.org/10.1021/jo702563n>
- Namboothiri Irishi N.N, Rastogi Namrata, Ganguly Bishwajit, Mobin Shaikh M, Cojocaru Miriam: Selectivities in the 1,3-dipolar cycloaddition of nitrile oxides to dicyclopentadiene and its derivatives. Tetrahedron 2004, 60, 1453. <https://doi.org/10.1016/j.tet.2003.12.026>
- Melsa Petr, Mazal Ctibor: ChemInform Abstract: π‐Facial Selectivity in 1,3‐Dipolar Cycloaddition Reactions of α‐Methylidene‐γ‐lactone (VII) Substituted by 4‐Methyl‐2,6,7‐trioxabicyclo[2.2.2]octan‐1‐yl Group in γ‐Position. ChemInform 2002, 33. <https://doi.org/10.1002/chin.200237112>
