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• W2000335143 abstract "[reaction: see text]. The use of the Z-configured vinylogous silyl ketene acetals in Mukaiyama aldol reactions is described. Isopropyl alcohol as scavanger and the use of tris(pentafluorophenyl)borane as the Lewis acid are required for obtaining the gamma-alkylated syn-product selectively. In cases of alpha-chiral aldehydes, Felkin-Anh selectivity was observed." @default.
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• W2000335143 date "2001-10-12" @default.
• W2000335143 modified "2023-09-27" @default.
• W2000335143 title "Rapid Access to Polyketide Scaffolds via Vinylogous Mukaiyama Aldol Reactions" @default.
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• W2000335143 doi "https://doi.org/10.1021/ol016677o" @default.
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