The Crystal Structure of 3-Methoxy-estra-1,3,5(10) triene-16aBrJ7aOH Dedicated to Professor Kate BOLL-DORNBEROER on the occasion of her 70th birthday The steroid 3-Methoxy-estra-1,3,5( lO)triene-l6aBr, 17aOH crystallizes in the orthorhombic space group P 2,2,2, with lattice constants a = 30.653( 5
Preparation of tritium labelled estetrol [estra-1,3,5(10)- triene-3,15α,16α,17β- tetrol 6,7-3H]
✍ Scribed by Jack Fishman; Henry Guzik
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- French
- Weight
- 242 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The preparation of the tritium labelled fetal metabolite estra‐1, 3, 5 (10)‐3, 15α, 16α, 17β‐tetrol 6,7‐^3^H is described. The material was prepared by oxidation of the tetrol tetraacetate lb to the 6‐keto derivative II. Reduction of the 6‐ketone to the 6‐hydroxy compound III and dehydration with dimethylsulfoxide gave the Δ6 derivative III. Reduction of III with tritium followed by hydrolysis gave the tetrol‐^3^H with a specific activity of 43 curies/mmole.
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## Abstract The nature of the reactions involved in the synthesis of 3‐cyclopentyloxy‐19‐nor‐17α‐pregna‐3, 5‐dien‐20‐yn‐17‐ol‐7‐^3^H 17‐acetate, allowed the determination of the stereochemistry of the tritium atoms at C‐6 in some of the precursors. One of these precursors was estra‐1, 3, 5 (6)‐trie
## Abstract The synthesis of a [9α, 11α‐]‐tritium‐labelled new steroid with interceptive — post‐coital antifertility — activity, 3‐methoxy‐14β, 15β‐methylene‐estra‐1,3,5(10)‐triene‐17β‐ol, starting with the catalytic tritiation of 3‐methoxy‐estra‐1,3,5(10), 9(11)‐tetraene‐14α, 17β‐diol, is describe