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

17Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

Mansot, J., Lauberteaux, J., Lebrun, A., Mauduit, M., Vasseur, J. J., Marcia de Figueiredo, R., … Smietana, M. (2020). DNA-Based Asymmetric Inverse Electron-Demand Hetero-Diels–Alder. Chemistry - A European Journal, 26(16), 3519–3523. https://doi.org/10.1002/chem.202000516

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free