Knoevenagel addition/ketalization intramolecular retro-Claisen cascade

In the amine-catalyzed reactions, a Knoevenagel addition/ketalization/ intramolecular retro-Claisen cascade is detected (Scheme 2.32). The retro-Claisen step is enabled by the ketalization of the Knoevenagel addition product Q. The ketalization of the Knoevenagel product (Q S) is initiated by the hydroxyl groups of the carbohydrate moiety, as in-house NMR-experiments suggest (formation of intermediate ketal structure K in Knoevenagel condensation/ketalization/oxa-Michael cascade reaction Scheme 2.16). Products derived from this reaction sequence (Scheme 2.16)... 

Similar to the mechanism described in Scheme 2.16, a Knoevenagel reac-tion/ketalization cascade of hydroxyacetone with 1,3-dicarbonyl compounds is assumed. In Scheme 2.16, a Knoevenagel condensation/ketalization reaction is depicted. This sequence allows a subsequent oxa-Michael addition, which yields the corresponding C-glycosides. In contrast, a Knoevenagel addition/ketalization occurs under the reaction condition described in Scheme 2.28, which is followed by an intramolecular retro-Claisen step. As a result of that, the corresponding esters were obtained (Scheme 2.29). 

To explain the high selectivity, which is detected in these cascade reactions, the possible products and reaction paths for reaction with L-erythrulose 146 and acety-lacetone 5 are depicted in Scheme 2.32. The stereoselective Knoevenagel addition to intermediate Q is favored and determines simultaneously the configuration of the tertiary alcohol. A subsequent ketalization step to ketone S followed by the final intramolecular retro-Claisen step yields the isolated product 147 as a single stereoisomer. 

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See also in sourсe #XX -- [ ]

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