Journal of Natural Products · 2013 · 29 citations · 19 references
AgricultureBiochemistryBioisosterismFruit ScienceNatural Product BiosynthesisFruit BiochemistryFruit RipeningAcid-catalyzed ReactionsAnalytical Chiral SeparationCarotenoid BiosynthesisCarotenoid ChemistryConfigurational AnalysisConfigurational AssignmentFruit PhytochemicalsPlant-derived Natural Products
New carotenoids, cryptocapsin-5,6-epoxide, 3'-deoxycapsanthin-5,6-epoxide, and cryptocapsin-5,8-epoxides, have been isolated from the ripe fruits of red mamey (Pouteria sapota). Cryptocapsin-5,6-epoxide was prepared by partial synthesis via epoxidation of cryptocapsin, and the (5R,6S)- and (5S,6R)-stereoisomers were identified by HPLC-ECD analysis. Spectroscopic data of the natural (anti) and semisynthetic (syn) derivatives obtained by acid-catalyzed rearrangement of cryptocapsin-5,8-epoxide stereoisomers were compared for structural elucidation. Chiral HPLC separation of natural and semisynthetic samples of cryptocapsin-5,8-epoxides was performed, and HPLC-ECD analysis allowed configurational assignment of the separated stereoisomers.
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Florence Bouvier, Philippe Hugueney, Alain d’Harlingue et al. · The Plant Journal · 1994 · 200 citations · Full text
Stereochemistry of atropisomeric 9,10-dihydrophenanthrene dimers from Pholidota chinensis
Sheng Yao, Chunping Tang, Yang Ye et al. · Tetrahedron Asymmetry · 2008 · 46 citations