Totalsynthese von Rameswaralid
Zusammenfassung der Projektergebnisse
The synthesis of chiral from racemic allenes constitutes a challenge in organic chemistry and the corresponding synthetic methods have been limited to kinetic resolutions of racemic allenes. In contrast, our methodology1 allows for the synthesis of structurally complex chiral allenes from readily available racemic allenes by palladium-catalysis. The reaction proceeds via a catalyst-controlled generation of a diastereomeric palladium/nucleophile complex and its addition to activated achiral electrophiles. That leads to absolute control of stereochemistry and substitution around the allene core with excellent levels of regio-, diastereo-, and enantiocontrol. Furthermore, we were able to demonstrate the involvement of a DYKAT process and a stepwise mechanism for the cycloaddition event. The densely functionalized chiral allenes were readily derivatized to a variety of useful molecules in a particularly step-economic manner.
Projektbezogene Publikationen (Auswahl)
- Enantio‐and Diastereoselective Synthesis of Chiral Allenes by Palladium ‐Catalyzed Asymmetric [3+ 2] Cycloaddition Reactions, Angew. Chem. Int. Ed. 2018, 57, 12916–12920
B. M. Trost, D. Zell, C. Hohn, G. Mata, A. Maruniak
(Siehe online unter https://doi.org/10.1002/anie.201808345) - Palladium-Catalyzed Asymmetric Allylic Fluoroalkylation/Trifluoromethylation, J. Am. Chem. Soc. 2019, 141, 11446–11451
B. M. Trost, H. Gholami, D. Zell
(Siehe online unter https://doi.org/10.1021/jacs.9b06231)
