Since the seminal work of Roelfes and Feringa in 2005,[1] DNA-based asymmetric catalysis has drawn increasing attention to become a particularly attractive tool for synthetic organic chemists. Indeed, DNA-based catalysts have now been successfully applied to a variety of asymmetric transformations including Diels–Alder cycloadditions,[1] Michael additions,[2] Friedel–Crafts alkylations,[3] fluorinations,[4] and syn-hydrations.[5, 6] More recently, the ...
[Willemsen, Jorgen S.; Megens, Rik P.; Roelfes, Gerard; Van Hest, Jan C. M.; Rutjes, Floris P. J. T. European Journal of Organic Chemistry, 2014 , vol. 2014, # 14 p. 2892 - 2898]
