Literature DB >> 33650626

α,β-Unsaturated acyl ammonium species as reactive intermediates in organocatalysis: an update.

Jacqueline Bitai1, Matthew T Westwood, Andrew D Smith.   

Abstract

α,β-Unsaturated acyl ammonium species are versatile intermediates that have been applied in a variety of transformations including Michael additions, domino reactions and cycloadditions. Many of these transformations are promoted by chiral Lewis base catalysts, enabling the rapid generation of molecular complexity with high stereochemical control. This review highlights recent developments in the generation and application of α,β-unsaturated acyl ammonium intermediates reported since a previous review of this area in 2016. Particular emphasis will be placed on reports providing mechanistic insight into catalytic transformations and observed selectivities. A perspective on current challenges and potential future developments in the field of α,β-unsaturated acyl ammonium catalysis is also provided.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 33650626     DOI: 10.1039/d0ob02208j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Esters.

Authors:  Jacqueline Bitai; Alastair J Nimmo; Alexandra M Z Slawin; Andrew D Smith
Journal:  Angew Chem Int Ed Engl       Date:  2022-04-28       Impact factor: 16.823

2.  Isothiourea-Catalyzed Enantioselective Michael Addition of Malonates to α,β-Unsaturated Aryl Esters.

Authors:  Jiufeng Wu; Claire M Young; Amy A Watts; Alexandra M Z Slawin; Gregory R Boyce; Michael Bühl; Andrew D Smith
Journal:  Org Lett       Date:  2022-06-02       Impact factor: 6.072

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.