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Showing papers by "Nobuaki Taniguchi published in 2010"



Journal ArticleDOI
TL;DR: In this article, an enantioselective synthesis of a 6-oxygenated atisine derivative was described, based on the intramolecular double Michael reaction of the enone ester derived through the aldehyde 3 from the symmetrical ketone 4.
Abstract: An enantioselective synthesis of a 6-oxygenated atisine derivative 20 is described. The atisine skeleton 18 was stereoselectively constructed by the intramolecular double Michael reaction of the enone ester 16, derived, through the aldehyde 3, from the symmetrical ketone 4.