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Asymmetric synthesis and absolute stereochemistry of 4,4-bis-(trifluoromethyl)imidazoline based ACAT inhibitors

โœ Scribed by Hui-Yin Li; Indawati DeLucca; Spencer Drummond; George A. Boswell


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
639 KB
Volume
53
Category
Article
ISSN
0040-4020

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โœฆ Synopsis


An asymmetric synthesis of 1, a potent orally active ACAT inhibitor, is reported.

The absolute configuration of 1 has been determined by exciton CD spectra and X-ray crystal structure analysis.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Singlet Oxygen Oxid
โœ H.-Y. LI; S. DRUMMOND; I. DELUCCA; G. A. BOSWELL ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 2 views

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