Abstract
The preparation of two η6-estra-1,3,5(10),6-tetraene tricarbonylchromium complexes 4 and 6 are described. In both cases only one stereoisomer can be isolated, in contrast to other estrane-tricarbonylchromium complexes, where complexations are non-stereoselective. X-ray crystal structural analysis of 4 discloses that only the more sterically hindered β-facial isomer is formed. It is assumed that the 6,7-olefinic moiety exerts a directive influence on the complexation.
| Original language | English |
|---|---|
| Pages (from-to) | 945-947 |
| Number of pages | 3 |
| Journal | Zeitschrift fur Anorganische und Allgemeine Chemie |
| Volume | 629 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2003 |
| Externally published | Yes |
Keywords
- Alkene
- Chromium
- Directive effects
- Steroids
- π-Facial selectivity
ASJC Scopus subject areas
- Inorganic Chemistry
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