A novel route to enantiomerically pure sulfoxides through displacement of a carbon leaving group

DOI: 10.1016/0040-4039(96)01264-6

Source and publish data:

Tetrahedron Letters p. 6017 - 6020 (1996)

Update date:2022-08-11

Topics:

Authors:

Cardellicchio, Cosimo

Iacuone, Antonio

Naso, Francesco

Tortorella, Paolo

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Article abstract of DOI:10.1016/0040-4039(96)01264-6

Enantiomerically pure sulfoxides were produced by reaction of dimethyl (S)-p-tolyl-sulfinylmethylphosphonate with the suitable Grignard reagents. Yields up to 75% were obtained.

Full text of DOI:10.1016/0040-4039(96)01264-6

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