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A New Class of Recoverable Chiral Sulphoxide: Application to the Asymmetric Synthesis of β-Hydroxy Esters.

DOI: 10.1016/S0040-4039(00)79112-X

Source and publish data:

Tetrahedron Letters p. 5427 - 5430 (1992)

Update date:2022-08-03

Topics:

Authors:

Wills, MartinWills, Martin

Butlin, Roger J.Butlin, Roger J.

Linney, Ian D.Linney, Ian D.

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Article abstract of DOI:10.1016/S0040-4039(00)79112-X

Enantiomerically pure cyclic sulphinamide S(S)R-(+)-2 was prepared from homochiral sulphinic acid R-(-)-1 and subsequently converted to the ester S(S)R-(-)-3 via ring opening with an ester enolate.Aldol reactions of S(S)R-

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Full text of DOI:10.1016/S0040-4039(00)79112-X

Products guided by the article

Product name:(S)-2-{(S)-2-[(R)-1-(2,2-Dimethyl-propionylamino)-ethyl]-benzenesulfinyl}-3-hydroxy-3-(2-methoxy-phenyl)-propionic acid tert-butyl ester

Cas No:144490-75-5

144490-75-5

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