Collect. Czech. Chem. Commun.
1993, 58, 2202-2210
https://doi.org/10.1135/cccc19932202
Synthesis of 17α-Hydroxy Steroids: B-Norepitestosterone
Alexander Kasal
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic
Crossref Cited-by Linking
- Ahmed Gulzar, Nickisch Klaus: Thermodynamic Meerwein-Ponndorf-Verley reduction in the diastereoselective synthesis of 17α-estradiol. Steroids 2016, 113, 1. <https://doi.org/10.1016/j.steroids.2016.04.006>
- Guo Peng-Peng, Ding Kai: Perfluoroalkylsulfonyl fluoride in organic synthesis: a facile synthesis of 17α-hydroxy steroids. Tetrahedron Letters 2015, 56, 4096. <https://doi.org/10.1016/j.tetlet.2015.05.026>
- Kasal Alexander, Krištofíková Zdena, Buděšínský Miloš: Neurosteroids: 7-aza-allopregnanolone—a poor substitute for allopregnanolone. Tetrahedron 2007, 63, 11355. <https://doi.org/10.1016/j.tet.2007.08.078>
- KASAL A.: ChemInform Abstract: Steroids. Part 369. Synthesis of 17α‐Hydroxy Steroids: B‐ Norepitestosterone. ChemInform 1994, 25. <https://doi.org/10.1002/chin.199403209>
- Velgová Helena, Kasal Alexander, Buděšínský Miloš: Some reactions of 16α,17α-oxido-5α-cholestane derivatives, synthesis of 17α-hydroxycholest-4-en-3-one. Steroids 1994, 59, 335. <https://doi.org/10.1016/0039-128X(94)90123-6>
