THREO SELECTIVE CROSS ALDOL CONDENSATION WITH THIOAMIDE ENOLATES GENERATED BY A MICHAEL ADDITION OF ORGANOMETALLICS TO UNSATURATED THIOAMIDES

DOI: 10.1016/S0040-4039(01)81688-9

Source and publish data:

Tetrahedron Letters p. 5793 - 5796 (1984)

Update date:2022-08-03

Topics:

Authors:

Tamaru, Y.

Hioki, T.

Yoshida, Z.

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Article abstract of DOI:10.1016/S0040-4039(01)81688-9

Crotonthioamide, sorbothioamide, and cinnamothioamide undergo a threo selective aldol condensation via their enolates generated by a Michael addition of organometallics.

Full text of DOI:10.1016/S0040-4039(01)81688-9

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