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- W3175884055 abstract "From the teaching class with the bispericyclic Diels–Alder reaction of ortho-quinols drawn on the chalk board to the laboratory with the (+)-ferruginol substrate and a chiral bisiodyl reagent in the flask: The single ortho-quinol diastereomer thus produced combines in pairs to reach a C2-symmetric transition state in which [4+2] and [2+4] processes are equivalent, as described by Laurent Pouységu, Stéphane Quideau, and co-workers in their Research Article on page 14967. Under high pressure, this transition state leads to the product, the natural (+)-maytenone, which was first isolated from the plant Maytenus dispermus, here appearing in the background image. Design by Jean Ung@SQuideau Lab." @default.
- W3175884055 created "2021-07-05" @default.
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- W3175884055 date "2021-05-17" @default.
- W3175884055 modified "2023-10-18" @default.
- W3175884055 title "Inside Back Cover: Bispericyclic Diels–Alder Dimerization of ortho ‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone (Angew. Chem. Int. Ed. 27/2021)" @default.
- W3175884055 doi "https://doi.org/10.1002/anie.202106111" @default.
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