✦ LIBER ✦

The benzilic acid rearrangement of 3α,17β-Diacetoxy-11-hydroxy-12-oxo-5β-androst-9(11)-ene

✍ Scribed by P. Kurath

Book ID: 112649353
Publisher: Springer
Year: 1966
Tongue: English
Weight: 231 KB
Volume: 22
Category: Article
ISSN: 1420-682X
DOI: 10.1007/bf01902425

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The molecular structure of the benzilic

The molecular structure of the benzilic acid rearrangement product of 3α, 17β-diacetoxy-11-hydroxy-12-oxo-5β-androst-9(11)-ene

✍ J. S. McKechnie; I. C. Paul 📂 Article 📅 1967 🏛 Springer 🌐 English ⚖ 236 KB

Correction. Structure and Stereochemistr

Correction. Structure and Stereochemistry of the Benzilic Acid Rearrangement Product of 3α,17β-Diacetoxy-11-hydroxy-5β-androst-9(11)-en-12-one

✍ Kurath, Paul 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 282 KB

The structure of the benzilic acid rearr

The structure of the benzilic acid rearrangement product of 3.alpha.,17.beta.-diacetoxy-11-hydroxy-12-oxo-5.beta.-androst-9(11)-ene. An unusual structure with three five-membered rings cis-fused

✍ McKechnie, James S.; Paul, Iain C. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 648 KB

The sulfuric acid induced fluorescence o

The sulfuric acid induced fluorescence of androst-4-ene-11β, 17α dihydroxy-5-oxo-17 carboxylic acid

✍ L.Gonçalves Sobrinho 📂 Article 📅 1966 🏛 Elsevier Science 🌐 English ⚖ 466 KB

(+)-4α,8α,14β-Trimethyl-18-nor-5α,13β-an

(+)-4α,8α,14β-Trimethyl-18-nor-5α,13β-androst-9(11)-en-3,17-dione, a synthetic precursor of fusidic acid

✍ Ward, D. L. ;Templeton, D. H. ;Zalkin, A. 📂 Article 📅 1973 🏛 International Union of Crystallography ⚖ 474 KB

Partial synthesis of a marine secosterol

Partial synthesis of a marine secosterol from Gersemia fruticosa: Preparation of the intermediate precursor 3β,6α-diacetoxy-24-methyl-12-oxo-5α-chol-9,11-en-24-oate

✍ Alexander Kuhl; Wolfgang Kreiser 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 207 KB

The conversion ofdesoxycholic acid (2) into the title compound 14 by 13 respectively 17 steps is described herein, including stereoselective construction of C-3 and C-6 hydroxy moieties and introduction of a A 9"lj double bond by dehydrogenation. 14 is believed to serve as a putative precursor for t