39765-16-7Relevant academic research and scientific papers
Total synthesis of E1 and E2 isoprostanes by diastereoselective protonation
Rodríguez, Ana R.,Spur, Bernd W.
, p. 9249 - 9253 (2007/10/03)
A short total synthesis of the E-type isoprostanes has been achieved using a two-component coupling process combined with a diastereoselective protonation under reagent control. Mild cleavage of the silyl protective groups with cat. BiBr3 or HF/Py followed by enzymatic hydrolysis of the methyl ester afforded the free E-type isoprostanes.
Synthesis of PGE1 and Various 10α-Hydroxyprostaglandins
Johnson, Carl R.,Chen, Yung-Fa
, p. 3352 - 3357 (2007/10/02)
Methods for the selective deprotection and/or reduction of compounds of type 2 to provide (7E)-7,8-didehydro-10α-hydroxy-PGE1, (7E)-7,8-didehydro-10α-hydroxy-PGF1, 10α-hydroxy-PGE1, 10α-hydroxy-PGF1, PGE1, and 15-epi-PGE1 as their racemic methyl esters have been examined.
