Conversion of an equilenane to the estrane: Synthesis of dl-3-methoxy-17β-carboxy-1,3,5(10)-estratriene
✍ Scribed by D.K. Banerjee; E.J. Jacob; Narain Mahishi
- Book ID
- 119481222
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- English
- Weight
- 302 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0039-128X
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A series of 3-O-phosphorylated analogs (4-10) of a novel bone-targeting estradiol analog (3) were synthesized after a thorough study of the reaction of 3 with a selection of phosphoryl chlorides under a variety of reaction conditions. Evaluation of these novel phosphate analogs for affinity for hydr
## Abstract The enantiomerically pure (+)‐3‐methoxy‐1, 3, 5 (10)‐estratrien‐11, 17‐dione **11** (with __trans‐anti‐trans__ configuration) was synthesized in a highly stereocontrolled fashion from (±)‐__t__‐butyl 4‐methoxy‐1‐benzocyclobutene carboxylate **(8)** and the (+)‐carboxylic acid **6**, obt