Possible Mechanism for the Stereoselective Double Michael Reaction Catalyzed by Trityl Perchlorate

DOI: 10.1246/cl.1988.1777

Source and publish data:

Chemistry Letters p. 1777 - 1780 (1988)

Update date:2022-09-26

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Authors:

Kobayashi, Shu

Sagawa, Yukihiro

Akamatsu, Hiroshi

Mukaiyama, Teruaki

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Article abstract of DOI:10.1246/cl.1988.1777

The trityl perchlorate catalyzed double Michael reaction forming six-membered ring compounds from α,β-unsaturated ketones and siloxydienes was shown to take place via a two step process.

Full text of DOI:10.1246/cl.1988.1777

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