| Literature DB >> 25942500 |
Nikolaos Kaplaneris1, Giorgos Koutoulogenis1, Marianna Raftopoulou1, Christoforos G Kokotos1.
Abstract
The synthesis of both trans- and cis-diastereomers of pyrrolidinine-thioxotetrahydropyrimidinone bearing either a fluorine or a hydroxyl group was accomplished. The new compounds were tested for their catalytic properties in a variety of asymmetric organic transformations and compared with the first generation catalyst. It was found that the new catalysts could efficiently catalyze the reactions in brine, without the use of organic solvent, and by employing an almost stoichiometric amount of reagents. Thus, the products were isolated by simple extractions, avoiding the use of chromatography in excellent yields, diastereoselectivities, and enantioselectivities.Entities:
Year: 2015 PMID: 25942500 DOI: 10.1021/acs.joc.5b00283
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354