1226-91-1Relevant articles and documents
In situ formed acetals facilitated direct Michael addition of unactivated ketones
Koppolu, Srinivasa Rao,Balamurugan, Rengarajan
, p. 1186 - 1192 (2017/02/10)
TfOH-promoted synthesis of 1,5-diketones by the Michael reaction of unactivated ketones with chalcones has been described. Acetals formed under HC(OMe)3/TfOH conditions generate the required enol-equivalents for a smooth Michael reaction. A wide array of symmetrical and unsymmetrical 1,5-diketones has been synthesised.
A new Br?nsted acid derived from squaric acid and its application to Mukaiyama aldol and Michael reactions
Cheon, Cheol Hong,Yamamoto, Hisashi
scheme or table, p. 3555 - 3558 (2009/10/26)
Bis-N-trifluoromethanesulfonyl squaramide was prepared as a new bench-stable strong Br?nsted acid and applied to the Br?nsted acid-catalyzed Mukaiyama aldol and Michael reactions with silyl enol ethers. The resulting Mukaiyama aldol products of aldehydes
The first michael addition of metal ketone enolates to α,β- unsaturated esters under catalytic conditions: Tin enolate with a catalytic amount of tetrabutylammonium bromide
Yasuda, Makoto,Ohigashi, Noriyuki,Shibata, Ikuya,Baba, Akio
, p. 2180 - 2181 (2007/10/03)
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