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Article

Angerer, S. von and Seidl, E. and Mannschreck, A. and Angerer, E. von and Wiegrebe, Wolfgang (1994) Dibenzo[a,f]quinolizines: syntheses and cytostatic activity in estrogen-sensitive tumor cells. Anti-cancer drug design 9 (1), pp. 25-40.

Polossek, T. and Ambros, R. and Angerer, S. von and Brandl, G. and Mannschreck, A. and Angerer, E. von (1992) 6-Alkyl-12-formylindolo[2,1-a]isoquinolines. Syntheses, estrogen receptor binding affinities, and stereospecific cytostatic activity. Journal of Medicinal Chemistry 35 (19), pp. 3537-3547.

Angerer, S. von and Brandl, G. and Mannschreck, Albrecht and Weimar, C. and Wiegrebe, Wolfgang (1992) Dibenzo[a,g]quinolizin-8-ones: synthesis, estrogen receptor affinities, and cytostatic activity. Anti-Cancer Drug Design 7, pp. 351-363.

Angerer, S. von and Angerer, E. von and Ambros, R. and Wiegrebe, Wolfgang (1992) Ring-cleavage of Phthalidisoquinoline Alkaloids by Ethyl Chloroformate. Archiv der Pharmazie 325, pp. 425-431.

Weimar, C. and Angerer, S. von and Wiegrebe, Wolfgang (1991) Methoxy- and Acetoxy-8-oxoberbines-Synthesis, Antitumor-Activity, and Interaction with DNA. Archiv der Pharmazie 324, pp. 509-518.

Weimar, C. and Angerer, S. von and Wiegrebe, Wolfgang (1991) Synthesis of C-13-Alkylated 8-oxoberberbines. Archiv der Pharmazie 324, pp. 907-912.

Angerer, S. von and Eibler, E. and Lee, D.-U. and Wiegrebe, Wolfgang (1989) Degradation of 1-Benzyl-1,2,3,4-tetrahydroisoquinolines (Laudanosine) with Ethyl chloroformate: Gedamer's Intermediate. Scientia Pharmaceutica (Sci. Pharm.) 57, pp. 1-6.

Ambros, R. and Angerer, S. von and Wiegrebe, Wolfgang (1988) C-12-Substituted Indolo [2,1-a]isoquinolines as Estrogen Receptor Affinic Cytostatic Agents. Archiv der Pharmazie 321, pp. 743-747.

Ambros, R. and Angerer, S. von and Wiegrebe, Wolfgang (1988) Synthesis and Antitumor Activity of Methoxy-indolo[2,1-a]isoquinolines. Archiv der Pharmazie 321, pp. 481-486.

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