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