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DNA-Based Asymmetric Inverse Electron-Demand Hetero-Diels-Alder.

Justine MansotJimmy LauberteauxAurélien LebrunMarc MauduitJean-Jacques VasseurRenata Marcia de FigueiredoStellios ArseniyadisJean-Marc CampagneMichael Smietana
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
While artificial cyclases hold great promise in chemical synthesis, this work presents the first example of a DNA-catalyzed inverse electron-demand hetero-Diels-Alder (IEDHDA) between dihydrofuran and various α,β-unsaturated acyl imidazoles. The resulting fused bicyclic O,O-acetals containing three contiguous stereogenic centers are obtained in high yields (up to 99 %) and excellent diastereo- (up to >99:1 dr) and enantioselectivities (up to 95 % ee) using a low catalyst loading. Most importantly, these results show that the concept of DNA-based asymmetric catalysis can be expanded to new synthetic transformations offering an efficient, sustainable, and highly selective tool for the construction of chiral building blocks.
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