Literature DB >> 31646689

Design and synthesis of a stereodynamic catalyst with reversal of selectivity by enantioselective self-inhibition.

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.
© 2019 The Authors. Chirality published by Wiley Periodicals, Inc.

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


  1 in total

1.  Efficient Amplification in Soai's Asymmetric Autocatalysis by a Transient Stereodynamic Catalyst.

Authors:  Oliver Trapp
Journal:  Front Chem       Date:  2020-12-09       Impact factor: 5.221

  1 in total

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