APA 6th Edition Zimmer, R., Baumann, K., Sperner, H., Schulz, G., Haidl, E. i Grassberger, M.A. (2005). Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit. Croatica Chemica Acta, 78 (1), 17-27. Preuzeto s https://hrcak.srce.hr/2661
MLA 8th Edition Zimmer, Reinhold, et al. "Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit." Croatica Chemica Acta, vol. 78, br. 1, 2005, str. 17-27. https://hrcak.srce.hr/2661. Citirano 26.02.2021.
Chicago 17th Edition Zimmer, Reinhold, Karl Baumann, Hildegard Sperner, Gerhard Schulz, Ewald Haidl i Maximilian A. Grassberger. "Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit." Croatica Chemica Acta 78, br. 1 (2005): 17-27. https://hrcak.srce.hr/2661
Harvard Zimmer, R., et al. (2005). 'Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit', Croatica Chemica Acta, 78(1), str. 17-27. Preuzeto s: https://hrcak.srce.hr/2661 (Datum pristupa: 26.02.2021.)
Vancouver Zimmer R, Baumann K, Sperner H, Schulz G, Haidl E, Grassberger MA. Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit. Croatica Chemica Acta [Internet]. 2005 [pristupljeno 26.02.2021.];78(1):17-27. Dostupno na: https://hrcak.srce.hr/2661
IEEE R. Zimmer, K. Baumann, H. Sperner, G. Schulz, E. Haidl i M.A. Grassberger, "Synthetic Modifications of Ascomycin. V. Access to Novel Ascomycin Derivatives by Replacement of the Cyclohexylvinylidene Subunit", Croatica Chemica Acta, vol.78, br. 1, str. 17-27, 2005. [Online]. Dostupno na: https://hrcak.srce.hr/2661. [Citirano: 26.02.2021.]
Sažetak Starting from the easily accessible 24-O-tert-butyldimethylsilyl-22(R)-dihydro-28-oxoascomycin, methodologies that allow replacement of the cyclohexylvinylidene moiety of ascomycin by various other substituents are described. In addition, a so far unknown reactivity of the masked tricarbonyl moiety of ascomycin towards a stabilized Wittig reagent is reported.