A Highly Stereoselective Synthesis of γ-Acyl-δ-lactones by the Trityl Perchlorate Catalyzed Tandem Michael-aldol Reaction

DOI: 10.1246/cl.1986.1805

Source and publish data:

Chemistry Letters p. 1805 - 1808 (1986)

Update date:2022-08-05

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Authors:

Kobayashi, Shu

Mukaiyama, Teruaki

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Article abstract of DOI:10.1246/cl.1986.1805

γ-Acyl-δ-lactones are prepared in the high yields with high stereoselectivities by the trityl perchlorate catalyzed tandem Michael-aldol reaction between α,β-unsaturated ketones, ketene silyl acetals, and aldehydes.

Full text of DOI:10.1246/cl.1986.1805

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