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- W2003000616 abstract "A series of disubstituted cyclopentanones have been synthesized by the intramolecular Stetter reaction. Racemic substrates containing one chiral center were used, allowing us the opportunity to observe a parallel kinetic resolution in the synthesis of 2,3- and 2,4-disubstituted cyclopentanones. The Stetter reaction of 2,5-disubstituted cyclopentanones proved to be substrate controlled, resulting in the selective formation of the cis-diasteromers with low ee." @default.
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- W2003000616 date "2005-06-01" @default.
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- W2003000616 title "The effect of pre-existing stereocenters in the intramolecular asymmetric Stetter reaction" @default.
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- W2003000616 doi "https://doi.org/10.1016/j.tet.2005.03.121" @default.
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