STEREOSELECTIVE ALDOL ADDITIONS TO α-ALKOXY ALDEHYDES USING THIOESTER SILYL KETENE ACETALS.

DOI: 10.1016/S0040-4039(00)95102-5

Source and publish data:

Tetrahedron Letters p. 2373 - 2376 (1985)

Update date:2022-08-11

Topics:

Authors:

Gennari, Cesare

Bernardi, Anna

Poli, Giovanni

Scolastico, Carlo

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Article abstract of DOI:10.1016/S0040-4039(00)95102-5

Relative stereochemistry (chelation) effectively controls internal stereochemistry (syn-anti) in the addition of thiopropionate equivalents to O-benzyl lactic aldehyde.

Full text of DOI:10.1016/S0040-4039(00)95102-5

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