ACYCLIC STEREOSELECTION. ERYTHROSELECTIVE ALDOL CONDENSATION OF 4-ACYL-2,3-DIHYDRO-4H-1,4-BENZOTHIAZINE AND 10-ACYLPHENOTHIAZINE.

DOI: 10.1016/S0040-4039(00)94302-8

Source and publish data:

Tetrahedron Letters p. 3883 - 3886 (1983)

Update date:2022-08-04

Topics:

Authors:

Babudri, F.

Di Nunno, L.

Florio, S.

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Article abstract of DOI:10.1016/S0040-4039(00)94302-8

The title amides undergo aldol-type cross-condensation providing aldols of exclusive erythro configuration.The preferred cis geometry of the precursor amide enolate is likely to be at origin of the erythro selection.

Full text of DOI:10.1016/S0040-4039(00)94302-8

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