Collect. Czech. Chem. Commun.
2000, 65, 708-716
https://doi.org/10.1135/cccc20000708
Stereoselective 1,3-Dipolar Cycloaddition of a Nitrile Ylide Photochemically Generated from 2,3-Diphenyl-2H-azirine to Substituted Methylene Lactones
Jakub Častulík, Jaroslav Jonas and Ctibor Mazal*
Department of Organic Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
Crossref Cited-by Linking
- 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>
- Melša Petr, Mazal Ctibor: 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. Collect. Czech. Chem. Commun. 2002, 67, 353. <https://doi.org/10.1135/cccc20020353>
- Častulı́k Jakub, Marek Jaromı́r, Mazal Ctibor: Synthesis of spiropyrrolidines and spiropyrrolizidines by 1,3-dipolar cycloadditions of azomethine ylides to substituted α-methylene-γ-lactones. Tetrahedron 2001, 57, 8339. <https://doi.org/10.1016/S0040-4020(01)00807-9>
- Castulik Jakub, Jonas Jaroslav, Mazal Ctibor: ChemInform Abstract: Stereoselective 1,3‐Dipolar Cycloaddition of a Nitrile Ylide Photochemically Generated from 2,3‐Diphenyl‐2H‐azirine to Substituted Methylene Lactones. ChemInform 2000, 31. <https://doi.org/10.1002/chin.200037042>
