Photoredox autocatalysis: towards a library of generally applicable reductive photocatalysts

23 July 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Dichotomous thinking dominates the field of synthetic photochemistry – either a reaction needs a photocatalyst or not. Herein, we report the discovery of photoredox autocatalytic pathway, a third mechanistic paradigm that is thus far overlooked, to access cyclic biaryl sulfonamides (BASNs). This reaction does not require exogenous catalyst as the visible light absorbing deprotonated product itself, with potent excited state reductive power, acts as the photocatalyst for its own synthesis. This finding implicated BASN as a novel organophotocatalyst architecture and allowed a rapid, modular, and low-cost combinatorial synthesis of a BASN library that expediated optimal photocatalyst screening. Furthermore, BASN was revealed as a general organophotocatalyst for a diverse set of transition metal-free transformations such as: intramolecular (spiro)-cyclizations, defunctionalizations, and C-C / C-heteroatom couplings.

Keywords

photocatalysis
autocatalysis
photoredox autocatalysis
autophotocatalysis
sulfonamide
biarylsultam
sultam
radicals
library
high-throughput screening
cyclization
defunctionalization
Heck
deoxygenation
dehalogenation

Supplementary materials

Title
Description
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Title
Supplementary Material File
Description
Synthetic procedures, listed compound data, computational investigations, further mechanistic investigations references
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Supplementary Material Spectra
Description
NMR spectra of compounds synthesized.
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