Synthesis of isomeric 16,17-epoxy-[17-3H)-derivatives of 3-hydroxy and 3-methoxy-oestra-1,3,5(10)-trienes
✍ Scribed by G. Michael Blackburn; Brian F. Taylor; Andrew F. Worrall
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- French
- Weight
- 373 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Deuterium NMR spectroscopy has been used to show that a previously published synthesis of t6d,17r-epoxy-3-hydroxy-~~-3H]oestra~~l,3,5(10)-triene is not regiospecific but leads to additional isotope incorporation at positions -2 and/or -4. A modified synthesis i s described which leads to the title compounds exclusively labelled at position -17.
📜 SIMILAR VOLUMES
## Abstract The four possible isomers of 16‐hydroxymethyl‐3‐methoxyestra‐1,3,5(10)‐trien‐17‐ol 5a, 6a, 7a, 8a were converted into the corresponding 16‐methyl analogues 4a, 11a, 12a, 13a, which were characterized from their ^1^H‐ and ^13^C‐NMR spectra. The results permit a configurational correlatio
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