Leucogenenol

Leucogenenol
Names
	Other names Leukogenenol
Identifiers
CAS Number	29101-95-9 ;
PubChem CID	301101;
CompTox Dashboard (EPA)	DTXSID90951698 ;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

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. doi:10.1039/j39710002599. PMID 5167554.
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 is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Rice, F. A. H. (1971). "Structure of leucogenenol". Journal of the Chemical Society C: Organic. 15: 2599–606. doi:10.1039/j39710002599. PMID 5167554.

[2] 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.

[3] 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.