𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The crystal structure of 21-bromo-9α-fluoro-11β-hydroxy-16α, 17α-(β-methyl-α-phenylmethylenedioxy)-4-pregnene-3.20, dione

✍ Scribed by Gerald W. Krakower; Barbara T. Keeler; J.Zanos Gougoutas

Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
205 KB
Volume
12
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Crystal and Molecular Structure of 3
The Crystal and Molecular Structure of 3-Oxo-17β-acetoxy-Δ4-14α-methyl-8α, 9β, 10α, 13α-estrene
✍ Gunji Koyama 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 German ⚖ 331 KB 👁 1 views

CH,(18) + 14-CH3; 2.07, s CH,( 4) (CDCI,);not yet crystalli~ed]~). Finally, 8 was converted by catalytic hydrogenation [5%-Pd/C in ethanol/triethylamine; + 11 and cyclisation [HCl in acetic acid] into 3-oxo-17~-acetoxy-14a-methyl-A4-8a,9B,lOa,13a-estrene (12) [m.p. 86-88'; -[ U ] D = + 1' (CHC1,).

Hormonal therapy in cancer of the breast
Hormonal therapy in cancer of the breast, XIII. The effect of 9α-fluoro-17α-methyl-Δ4-androsten-3-one-11β,17β-diol (fluoxymesterone) therapy on clinical course and hormonal excretion
✍ Albert Segaloff; C. Y. Bowers; Edward L. Rongone; Paul J. Murison; Joseph V. Sch 📂 Article 📅 1958 🏛 John Wiley and Sons 🌐 English ⚖ 263 KB 👁 1 views

HE ANDROGENIC steroids most effective in T the treatment of metastatic breast cancer have all been potent androgens. T o date, the less potent androgens have been less effective.3~4 Hence, when an androgen more potent than testosterone or methyltestosterone became available it was thought important

Preparation of high specific activity tr
Preparation of high specific activity tritium labeled 6α,9,-difluoro-11β,21-dihydroxy-16α,17-[(1-methylethylidene)bis(oxy)]pregna-1,4-diene-3,20-one, fluocinolone acetonide
✍ D. Zhong; Anita H. Lewin 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 289 KB

## Abstract Fluocinolone acetonide was tritiated by selective reduction of the 1,2‐double bond of the __O__‐protected analog under tritium, followed by re‐establishment of the 1,2‐double bond and deprotection. Protection of both hydroxyl functionalities was required. The product was obtained with s

Crystal Structure of R 29490, an N-methy
Crystal Structure of R 29490, an N-methylated Analog of a Potent Steroidic Gaba-A Antagonist: 3α-Hydroxy-16-Imino-5β-17-Aza-Androstan-11-One, R 5135
✍ Thierry Boulanger; Daniel P. Vercauteren; Guy Evrard; François Durant 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 190 KB

The synthesis of gornma-aminobutyric acid (GABA) receptor ligands is important in finding new therapeutic agerts and in helping to understand the mode of action of GABA. Amongst others, the steroid derivative 3a-hydroxy-