Leucogenenol
| Names | |
|---|---|
| Other names
Leukogenenol
| |
| Identifiers | |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Leucogenenol is a blood cell stimulating secondary metabolite isolated from the mold Penicillium gilmanii. Its chemical structure was reported;[1] however, later studies determined that the original structure is incorrect and the true chemical structure of leucogenenol remains unknown.[2][3]
References
- ^ Rice, F. A. H. (1971). "Structure of leucogenenol". Journal of the Chemical Society C: Organic. 15: 2599–606.
- ^ Salomon, Robert G.; Salomon, Mary F.; Zagorski, Michael G.; Reuter, James M.; Coughlin, Daniel J. (1982). "Total synthesis refutes the postulated structure of leucogenenol". Journal of the American Chemical Society. 104 (4): 1008–13. doi:10.1021/ja00368a015.
- ^ Aberhart, D. John; Clardy, Jon; Ghoshal, Pallab K.; Cunheng, He; Zheng, Qitai (1984). "Synthesis of 3-hydroxy-3-(hydroxymethyl)-5-methylcyclohexane-1,2-dione dibenzoate, a reported hydrolytic degradation product of leucogenenol". Journal of Organic Chemistry. 49 (13): 2429–33. doi:10.1021/jo00187a026.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |