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Synthesis and Stereochemical Behavior of Ketoester Derivatives having trans -Cyclononene Skeleton

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Abstract It has been found that the enolate formation followed by the alkylation of cyclic ketoester 2 provides (pR*, S*)-1 predominantly as a kinetic product. Planar chirality of 1 is labile at ambient temper...ature, hence (pR*, S*)-1 easily isomerizes to thermodynamically more favorable (pS*, S*)-1.show more

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Created Date 2010.11.16
Modified Date 2020.11.27

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