## Abstract Benzene oxide ‐[U‐^14^C] was prepared from benzene ‐(U‐^14^C) by modifications of methods described for the inactive compound. Benzene oxide‐[3.6–^3^H] was prepared by decomposition of 3.6‐bis‐trimethylsilyl‐1,4‐cyclohexadiene with tritiated water. bromination of the 1,4‐cyclohexadiene
Preparation of 3H- and 14C-labelled contraceptive steroids
✍ Scribed by Kenyu Shibata; Yoshio Osawa; Avery A. Sandberg
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- French
- Weight
- 236 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^3^H‐ and ^14^C‐Labelled ethynodiol diacetate, chlormadinone acetate, and medroxyprogesterone acetate with one label at the steroid nucleus and the other at the acetoxy group were prepared for use in studies of regio‐ and stereospecificity of metabolic hydrolysis of the steroid contraceptives. Steroidal secondary, tertiary, equatorial, and axial acetates were labelled under selective conditions using acetic anhydride.
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## Abstract A convenient method for preparing 5__H__‐2,3‐benzodi‐azepines labelled with ^14^C was developed in which the corresponding phenylacetone derivatives were acylated by labelled aromatic carboxylic acid. In spite of the low yield, this method is advantageous in comparison the known ones be
## Abstract 7,8‐Didehydro‐4,5‐epoxy‐3‐ethoxy‐17‐methyl(^3^H)‐, and −17‐methyl (^14^C)morphinan‐6‐ol were prepared by substituting the N‐methyl group with/^a^carbphenoxy group which was then either reduced with LiAl^3^H~4~ or removed to remethylate the N‐atom with ^14^CH~3~I.
3H-Sch 47949, racemic 3H-Sch 48461, was prepared at a specific activity of 40 mCi/mmole by Pt catalysed exchange with tritiated water. 3H-Sch 48461 was prepared at a specific activity of 64.6 Ci/mmole by a Pd/C catalysed reduction of an olefinic intermediate. 14C-Sch 48461 was prepared in 8 steps fr