✦ LIBER ✦

Synthesis of Δ5,22-cholestadien-3β-ol from Δ5,7,22-cholestatrien-3β-ol by a liver enzyme

✍ Scribed by Mary J. Koroly; Mary E. Dempsey

Book ID: 112773476
Publisher: Springer-Verlag
Year: 1981
Tongue: English
Weight: 258 KB
Volume: 16
Category: Article
ISSN: 0024-4201
DOI: 10.1007/bf02535344

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Endogenous Formation of Δ 5,7,24 -Choles

Endogenous Formation of Δ 5,7,24 -Cholestatrien-3βol

✍ Dvornik, D.; Kraml, M.; Bagli, J. F. 📂 Article 📅 1964 🏛 American Chemical Society 🌐 English ⚖ 439 KB

Δ5,7,9(11)-cholestatrien-3β-ol: A fluore

Δ5,7,9(11)-cholestatrien-3β-ol: A fluorescent cholesterol analogue

✍ Robert T. Fischer; Frances A. Stephenson; Ali Shafiee; Friedhelm Schroeder 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 659 KB

Synthesis of 20,22-epoxybisnor-δ5-cholen

Synthesis of 20,22-epoxybisnor-δ5-cholen-3β-ol

✍ Zh. S. Sydykov; G. M. Segal' 📂 Article 📅 1976 🏛 Springer 🌐 English ⚖ 226 KB

STEROIDAL SAPOGENINS. V. Δ 5,7 -22-ISOSP

STEROIDAL SAPOGENINS. V. Δ 5,7 -22-ISOSPIROSTADIEN-3β-OL 1

✍ ROSENKRANZ, G.; ROMO, J.; BERLIN, J. 📂 Article 📅 1951 🏛 American Chemical Society 🌐 English ⚖ 526 KB

The Anthrasteroid Rearrangement. VIII. 1

The Anthrasteroid Rearrangement. VIII. 1 The Rearrangement of Dehydroergosterol and Δ 5,7,9(11) -Cholestatriene-3β-ol to Δ 5,7,9,22 -Anthraergostatetraen-x-ols and Δ 5,7,9 -Anthracholestatrien-x-ols

✍ Tsuda, Kyosuke.; Hayatsu, Ryoichi.; Steele, John A.; Tanaka, Osamu.; Mosettig, E 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 880 KB

New syntheses of theΔ5,22 cis and trans

New syntheses of theΔ5,22 cis and trans C26 and C27 sterols dimethyl-24 chola-5, 22 dien-3β OL and cholesta-5,22 dien-3β OL

✍ A. Metayer; A. Quesneau-Thierry; M. Barbier 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 202 KB

## Previous syntheses of the title sterols have lead to mixtures of theirn22 tie and trans isomersl' 2. We wish to report now3 new syntheses of the two compounds and the