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A stereocontrolled total synthesis of 2β,3β,20β-triacetoxy-5α-pregnan-6-one — A total synthesis of 20-hydroxyecdysone

✍ Scribed by Tetsuji Kametani; Masayoshi Tsubuki; Hideo Nemoto


Book ID
107858226
Publisher
Elsevier Science
Year
1980
Tongue
French
Weight
131 KB
Volume
21
Category
Article
ISSN
0040-4039

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THE total synthesis of several steroids (1.2) has previously been reported from this laboratory. In this communication a straightforward total synthesis of rec. 5a-preQnan-3~-ol-20-one (XIIIa) is reported. '3 All melting points were measured on Kofler block and corrected. '

Synthesis of 5α-pregnane-3β,20α-diol and
✍ T. A. Baillie; J. E. Herz; J. Sjövall 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 French ⚖ 241 KB 👁 1 views

## Abstract A convenient synthesis of 5α‐[20β‐^2^H]pregnane‐3α,20α‐diol and 5α‐[20β‐^2^H]pregnane‐3β,20α‐diol from 3β‐hydroxy‐5α‐pregn‐16‐en‐20‐one is described. The reaction products are characterized by combined gas chromatography‐mass spectrometry.