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(a) Drabowicz, J.; Kiełbasiński, P.; Mikołajczyk, M. in The Synthesis of Sulphones and Sulphoxides and Cyclic Sulphides; Patai, S., Rappoport, Z., Stirling, C. J. M., Eds.; John Wiley and Sons: New York, 1994; pp 109-388.
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(a) Abbott, D. J.; Colonna, S.; Stirling, C. J. M. J. Chem. Soc. D 1971, 472-473; J. Chem. Soc., Perkin Trans 1 1976, 492-498.
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(a) Abbott, D. J.; Colonna, S.; Stirling, C. J. M. J. Chem. Soc. D 1971, 472-473; J. Chem. Soc., Perkin Trans 1 1976, 492-498.
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Block, E., Ed.; JAI Press Inc.: Greenwich, CT
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For a recent review on α-phosphoryl sulfoxides see: Mikołajczyk, M.; Bałczewski, P. In Advances in Sulfur Chemistry; Block, E., Ed.; JAI Press Inc.: Greenwich, CT, 1994; Vol. 1, pp 41-96.
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Bałczewski, P.2
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Similarly, the Craig's one-pot modification of the Horner-Wittig reaction results in various ratios of geometrical isomers of α,β-unsaturated sulfoxides: Craig, D.; Daniels, K.; McKenzie, A. R. Tetrahedron 1993, 49, 11263-11304.
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Interestingly, Z-vinyl sulfoxides can be transformed into their E-isomers without racemization at sulfur via lithiation and protonation: Fawcett, J.; House, S.; Jenkins, P. R.; Lawrance, N. J.; Russell, D. R. J. Chem. Soc., Perkin Trans, 1 1993, 67-73.
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Solladie, G. Synthesis 1981, 185-196. (-)-(S)-menthyl p-toluenesulfinate (4b) was obtained from (-)-(1R,2S,5R)-menthol.
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For a relationship between the chirality at sulfur, E,Z-geometry, and sign of optical rotation in α,β-unsaturated sulfoxides, see: Mikołajczyk, M.; Midura, W. H.; Wladislaw, B.; Biaggio, F. C.; Marzorati, L. Tetrahedron 1997, 53, 2959-2972.
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Tetrahedron
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(a) Drabowicz, J.; Dudziński, B.; Mikołajczyk, M.; Tetrahedron: Asymmetry 1992, 3, 1231-1232.
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