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- W2020164536 abstract "Amphiphilic calix[6]arene derivatives 1a−b and calix[4]arene 1d−1e, as well as aliphatic (2a−b) and aromatic (2c−2d) anionic surfactants, were studied for their encapsulating ability in stabilizing water-sensitive compounds. They were found to be efficient surfactants for Sc(OTf)3-catalyzed Mukaiyama aldol reactions of labile enol ethers with aldehydes in water. The results indicate that a hydrophobic microenvironment was formed in the reaction system with either the amphiphilic calix[6]arene derivatives or the simple aromatic surfactants, which could encapsulate and stabilize some labile silyl enol ethers and thus promote the reactions." @default.
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- W2020164536 date "2002-05-04" @default.
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- W2020164536 title "Development of Highly Effective Encapsulating Surfactants for Mukaiyama Aldol Reactions in Water" @default.
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- W2020164536 doi "https://doi.org/10.1021/ie010782k" @default.
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