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Sulfoximines. -Compared with the corresponding neomenthyl analogues bornyl sulfoximines, e.g. (II), do not improve the enantiomeric excess in the formation of oxiranes such as (III) and (V). Replacement of the N-tosyl group in neomenthyl analogues by a bulkier camphor-10-sulfonyl residue does not improve the results. The structures of chiral sulfur compounds together with their corresponding epimers on sulfur are determined by X-ray analysis. -(TAJ, S. S.; SHAH, A. C.; LEE, D.; NEWTON, G.; SOMAN, R.; Tetrahedron: