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Diastereoselective Synthesis of Highly Functionalized Proline Derivatives.

Anna N PhilippovaDaria V VorobyevaPavel S GribanovFedor M DolgushinSergey N Osipov
Published in: Molecules (Basel, Switzerland) (2022)
An efficient way to access highly functionalized proline derivatives was developed based on a Cu(I)-catalyzed reaction between CF 3 -substituted allenynes and tosylazide, which involved a cascade of [3 + 2]-cycloaddition/ketenimine and a rearrangement/Alder-ene cyclization to afford the new proline framework with a high diastereoselectivity.
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