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ChemInform Abstract: Singlet Oxygen Oxidation of Pyrroles: Synthesis and Chemical Transformations of Novel 4,4-Bis(trifluoromethyl)imidazoline Analogues.

✍ Scribed by H.-Y. LI; S. DRUMMOND; I. DELUCCA; G. A. BOSWELL


Publisher
John Wiley and Sons
Year
2010
Weight
32 KB
Volume
28
Category
Article
ISSN
0931-7597

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✦ Synopsis


Singlet Oxygen Oxidation of Pyrroles: Synthesis and Chemical Transformations of Novel 4,4-Bis(trifluoromethyl)imidazoline Analogues.

-A new method to prepare 4,4-bis(trifluoromethyl)imidazolines is described via facile photooxidative cleavage of the pyrrole (I) with singlet oxygen. In addition, it is shown that MCPBA-mediated oxidation of the pyrrole (I) also gives 4,4-bis(trifluoromethyl)imidazole, but in low yields. The imidazoles (IV) and (VI) show good activity as ACAT inhibitors and cholesterol biosynthesis inhibitors.


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