TiIV??Catalyzed Asymmetric Sulfenylation of 1, 3??Dicarbonyl Compounds
M Jereb, A Togni
Index: Jereb, Marjan; Togni, Antonio Chemistry - A European Journal, 2007 , vol. 13, # 33 p. 9384 - 9392
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Citation Number: 32
Abstract
Abstract The electrophilic enantioselective sulfenylation of 1, 3-dicarbonyl compounds with phenylsulfenyl chloride is effectively catalyzed by [Ti (TADDOLato)] complexes. The corresponding products are obtained in moderate to high yields. The highest ee values (up to 97%) are obtained in toluene at room temperature and with a typical catalyst loading of 5 mol%. Bulky ester groups and sterically undemanding substituents at the α-position were ...
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