cheminform abstract: new chiral hypervalent iodine compounds in asymmetric synthesis

1
1999 stereochemistry stereochemistry (general, optical resolution) O 0030 12 - 034 New Chiral Hypervalent Iodine Compounds in Asymmetric Synthe- sis. Some new compounds of type (VI) are prepared and their use as electrophilic reagents in the asymmetric dioxytosylation of styrene and in the α-oxytosylation of propiophenone is reported. Up to 53% e.e. are obtained for the most effective iodine compound (VIa). The X-ray structural analysis of one iodine compound shows a strong interaction of the oxygen of the methoxy group and the iodine. — (HIRT, URS H.; SPINGLER, BERNHARD; WIRTH, THOMAS; J. Org. Chem. 63 (1998) 22, 7674-7679; Inst. Org. Chem., Univ. Basel, CH-4056 Basel, Switz.; EN) 1

Upload: urs-h-hirt

Post on 06-Jun-2016

215 views

Category:

Documents


3 download

TRANSCRIPT

1999 stereochemistry

stereochemistry (general, optical resolution)O 0030

12 - 034New Chiral Hypervalent Iodine Compounds in Asymmetric Synthe-sis. — Some new compounds of type (VI) are prepared and their use aselectrophilic reagents in the asymmetric dioxytosylation of styrene and in theα-oxytosylation of propiophenone is reported. Up to 53% e.e. are obtained forthe most effective iodine compound (VIa). The X-ray structural analysis ofone iodine compound shows a strong interaction of the oxygen of the methoxygroup and the iodine. — (HIRT, URS H.; SPINGLER, BERNHARD; WIRTH,THOMAS; J. Org. Chem. 63 (1998) 22, 7674-7679; Inst. Org. Chem., Univ.Basel, CH-4056 Basel, Switz.; EN)

1