28487-73-2Relevant articles and documents
IMPROVED SYNTHESIS OF 1,2,4-TRIAZOLINE-3,5-DIONE DERIVATIVES OF ERGOSTEROL AND A NEW METHOD FOR THEIR RECONVERSION TO ERGOSTEROL
Barton, Derek H. R.,Lusinchi, Xavier,Ramirez, Jesus Sandoval
, p. 2995 - 2998 (1983)
The ergosterol diene system reacts in excellent yield with a series of 4-substituted 1,2,4-triazoline-3,5-diones generated by in situ oxidation of the appropriate hydrazides with phenylseleninic anhydride or phenylseleninic acid.Diaryltelluroxide and diphenylselenoxide are also efficient oxidants.The diene system can be smoothly regenerated by alkaline hydrolysis.
Protection of the diene system of ergosterol by formation of urazole adducts: Comparative action of phenylaleninic anhydride on urazole derivatives and ergosterol: Influence of structure of the adduct
Barton,Lusinchi,Sandoval Ramirez
, p. 849 - 858 (2007/10/02)
-