Issue 46, 2021

Ternary complexes of chiral disulfonimides in transfer-hydrogenation of imines: the relevance of late intermediates in ion pair catalysis

Abstract

In ion pairing catalysis, the structures of late intermediates and transition states are key to understanding and further development of the field. Typically, a plethora of transition states is explored computationally. However, especially for ion pairs the access to energetics via computational chemistry is difficult and experimental data is rare. Here, we present for the first time extensive NMR spectroscopic insights about the ternary complex of a catalyst, substrate, and reagent in ion pair catalysis exemplified by chiral Brønsted acid-catalyzed transfer hydrogenation. Quantum chemistry calculations were validated by a large amount of NMR data for the structural and energetic assessment of binary and ternary complexes. In the ternary complexes, the expected catalyst/imine H-bond switches to an unexpected O–H–N structure, not yet observed in the multiple hydrogen-bond donor–acceptor situation such as disulfonimides (DSIs). This arrangement facilitates the hydride transfer from the Hantzsch ester in the transition states. In these reactions with very high isomerization barriers preventing fast pre-equilibration, the reaction barriers from the ternary complex to the transition states determine the enantioselectivity, which deviates from the relative transition state energies. Overall, the weak hydrogen bonding, the hydrogen bond switching and the special geometrical adaptation of substrates in disulfonimide catalyst complexes explain the robustness towards more challenging substrates and show that DSIs have the potential to combine high flexibility and high stereoselectivity.

Graphical abstract: Ternary complexes of chiral disulfonimides in transfer-hydrogenation of imines: the relevance of late intermediates in ion pair catalysis

Supplementary files

Article information

Article type
Edge Article
Submitted
08 Jūl. 2021
Accepted
22 Okt. 2021
First published
17 Nov. 2021
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2021,12, 15263-15272

Ternary complexes of chiral disulfonimides in transfer-hydrogenation of imines: the relevance of late intermediates in ion pair catalysis

M. Žabka and R. M. Gschwind, Chem. Sci., 2021, 12, 15263 DOI: 10.1039/D1SC03724B

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements