The intramolecular, stereoselective addition of sulfoximine carbanions to electron deficient alkenes

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The intramolecular, stereoselective addition of sulfoximine carbanions to electron deficient alkenes

Please use this identifier to cite or link to this item: http://hdl.handle.net/10355/2199

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Title: The intramolecular, stereoselective addition of sulfoximine carbanions to electron deficient alkenes
Author: Sikervar, Vikas; Harmata, Michael, 1959-
Contributor: University of Missouri-Columbia. Office of Undergraduate Research
Keywords: chiral benzothiazine
enantiomerically pure compounds
sulfoximine carbanions
general electron deficient alkenes
Date: 2005
Publisher: University of Missouri--Columbia. Office of Undergraduate Research
Abstract: Chiral Benzothiazine play important roles in synthetic organic chemistry since they can be used in the preparation of enantiomerically pure compounds. We have studied the synthesis of these species using the intramolecular, stereo selective addition of sulfoximine carbanions to general electron deficient alkenes. Details on the synthesis of starting material and cyclization reaction will be presented.
URI: http://hdl.handle.net/10355/2199

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