ENANTIOSELECTIVE CROSS ALDOL REACTION VIA DIVALENT TIN ENOLATE

DOI: 10.1246/cl.1982.1441

Source and publish data:

Chemistry Letters p. 1441 - 1444 (1982)

Update date:2022-07-30

Topics:

Authors:

Iwasawa, Nobuharu

Mukaiyama, Teruaki

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Article abstract of DOI:10.1246/cl.1982.1441

Highly enantioselective cross aldol reaction between aromatic ketones and various aldehydes is achieved via divalent tin enolates employing chiral diamines derived from (S)-proline as ligands.

Full text of DOI:10.1246/cl.1982.1441

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