## Abstract This report describes an efficient stereoselective synthesis of [11β‐^3^H]prostaglandin E~1~ ([11β‐^3^H]PGE~1~). The key multiply protected 11‐keto intermediate was prepared in only three steps from PGE~1~. Reduction of the ketone function at C‐11 with sodium borodeuteride and sodium bo
Stereoselective Synthesis of 8-Aza-9,11-ethenoprostaglandin H1
✍ Scribed by Barco, Achille ;Benetti, Simonetta ;Baraldi, Pier Giovanni ;Moroder, Fabio ;Pollini, Gian Piero ;Simoni, Daniele
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 309 KB
- Volume
- 1982
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
A stereoselective synthesis of the title compound [8‐aza‐9,11‐etheno‐PGH~1~ (3)] starting from butyl 2‐(p‐tolylsulfonyl)‐2‐azabicyclo[2.2.1]hept‐5‐ene‐exo‐3‐carboxylate (5) is described.
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