A horner-wadsworth-emmons approach to [(S)R]-4-substituted 1-p-tolylsulfinyl-1,3-dienes

Arce, Eva; Carreño, M. Carmen; Cid, M. B.; Ruano, JoséL. García

doi:10.1016/0957-4166(95)00221-a

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Sulfinyl Dienes1

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Cited by 13 publications

(1 citation statement)

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“…Sulfinyldienes can be prepared by Horner-Wadsworth-Emmons type chemistry. 96 Similar compounds have also been synthesised via Stille coupling of halovinyl sulfoxides, partial hydrogenation of sulfinyl enynes or vinylcupration of sulfinyl alkynes. 97 The formation of the corresponding iron(0) tricarbonyl complexes is also described.…”

Section: Sulfinyl Dienesmentioning

confidence: 99%

Recent developments in chiral non-racemic sulfinyl group chemistry in asymmetric synthesis

Hanquet¹,

Colobert²,

Lanners³

et al. 2003

Arkivoc

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Chiral sulfinyl groups have been widely used in organic synthesis as a stereo-and enantiodirecting functionality and the high efficiency of the selectivity has received much attention in recent years. In this review we wish to cover the work published in the literature since 1996. The participation of a chiral sulfinyl function in a wide range of reactions as well as the application of these methodologies to the synthesis of natural products are reported.

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Section: Sulfinyl Dienesmentioning

confidence: 99%