Reduction of 7-chlorobicyclo[3.2.0]hept-2-en-6-ones catalysed by 3α, 20β-hydroxysteroiddehydrogenase
✍ Scribed by H. Geoff Davies; Thomas C.C. Gartenmann; Jeff Leaver; Stanley M. Roberts; Michael K. Turner
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 110 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The enzymes are stirred together with Eupergit-C (Dumas Chemicals) in 1M phosphate buffer (pH 7.5) over 96 h at 4OC. 10. 7endo-Chloro-7exo-methylbicyclo[3.2.0]hept-2~en-6-one was reduced by HSDH to give optically pure-&do-alcohol.
📜 SIMILAR VOLUMES
An Efficient Synthesis of Bicyclo[3.3.0]oct-2-en-4-ones and 2-Azabicyclo[3.3.0]oct
## Abstract On ^1^n,π\*‐excitation, the title compound **2** undergoes a photoinduced intramolecular [4 + 2]‐cycloaddition affording the tetracyclic enol ether **3** as the only product in 79% yield. The assigned structure of **3** was confirmed by its conversion to the __p__‐nitrobenzoate **6** wh