Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1991, 56, 1052-1063
https://doi.org/10.1135/cccc19911052

11,13-Methylenation of sesquiterpene exomethylene-γ-lactones: Synthesis of sesquiterpene cyclopropyl-γ-lactones

Giovanni Appendinoa,*, Elisabetta Ghilardia, Giancarlo Cravottoa and Pierluigi Gariboldib

a Dipartimento di Scienza e Tecnologia del Farmaco, C. so Raffaello 31, 10125 Torino, Italy
b Dipartimento di Scienze Chimiche, Via S. Agostino 1, 62032 Camerino (MC), Italy

Crossref Cited-by Linking

  • Hansen Jacob C., Rabuffetti Marco, Bunch Lennart: Convenient access to β-substituted cysteines and β- and γ-mercapto prolines. Can. J. Chem. 2023, 101, 326. <https://doi.org/10.1139/cjc-2022-0161>
  • Singh Meenakshi, Ravichandiran V., Bharitkar Yogesh P., Hazra Abhijit: Natural Products Containing Olefinic Bond: Important Substrates for Semi-synthetic Modification Towards Value Addition. COC 2020, 24, 709. <https://doi.org/10.2174/1385272824666200312125734>
  • 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>
  • APPENDINO G., GHILARDI E., CRAVOTTO G., GARIBOLDI P.: ChemInform Abstract: 11,13‐Methylenation of Sesquiterpene Exomethylene‐γ‐lactones: Synthesis of Sesquiterpene Cyclopropyl‐γ‐lactones. ChemInform 1991, 22. <https://doi.org/10.1002/chin.199133250>