| Literature DB >> 31646689 |
Jan Felix Scholtes1,2, Oliver Trapp1,2.
Abstract
Chirality plays a pivotal role in an uncountable number of biological processes, and nature has developed intriguing mechanisms to maintain this state of enantiopurity. The strive for a deeper understanding of the different elements that constitute such self-sustaining systems on a molecular level has sparked great interest in the studies of autoinductive and amplifying enantioselective reactions. The design of these reactions remains highly challenging; however, the development of generally applicable principles promises to have a considerable impact on research of catalyst design and other adjacent fields in the future. Here, we report the realization of an autoinductive, enantioselective self-inhibiting hydrogenation reaction. Development of a stereodynamic catalyst with chiral sensing abilities allowed for a chiral reaction product to interact with the catalyst and change its selectivity in order to suppress its formation, which caused a reversal of selectivity over time.Keywords: asymmetric catalysis; autoinduction; chirality transfer; ligand design; noncovalent interaction; tropos ligands
Year: 2019 PMID: 31646689 DOI: 10.1002/chir.23132
Source DB: PubMed Journal: Chirality ISSN: 0899-0042 Impact factor: 2.437