Collect. Czech. Chem. Commun.
1991, 56, 1064-1069
https://doi.org/10.1135/cccc19911064
New way to digitoxigenin from 3β-acetoxy-5-androsten-17-one. Stereoselective free radical substitution of iodide atom by nitrile group as a key step
Andrzej Robert Daniewski, Marek Michal Kabat, Marek Masnyk, Wanda Wojciechowska and Jerzy Wicha*
Institute of Organic Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Poland
Individual author index pages
Other CCCC articles of these authors
- Agnieszka Przezdziecka, Alicja Kurek-Tyrlik and Jerzy Wicha*
Pd-Catalyzed Cross-Coupling Reaction of Sterically Hindered Vinyl Iodides and Organozinc Reagents. Synthesis of Vitamin D Analogues with an Aromatic Ring Attached at C-17
2002, Vol. 67, Issue 11, pp. 1658–1668 [Abstract] - Rafał Barycki, Maria Gumułka, Marek Masnyk, Włodzimierz M. Daniewski*, Mirosław Kobus and Mirosław Łuczak
Synthesis of N-Acetyl-3-phenylisoserinates of Sesquiterpenoid Alcohols of Lactarius Origin
2002, Vol. 67, Issue 1, pp. 75–82 [Abstract] - Alicja Kurek-Tyrlik, Kazimierz Minksztym and Jerzy Wicha
Towards Synthesis of Calysterols, Marine Sterols with Cyclopropene Moiety in the Side Chain: Synthesis of 26,27-Dinor-23H-isocalysterol
1998, Vol. 63, Issue 10, pp. 1575–1588 [Abstract]
