Triplet Excited Nitroarene Converts Linear Alkynes to Bent Ketones by Deleting a Carbon Atom

21 December 2023, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Alkynes are rarely modified using visible light catalysis employing molecular editing techniques. In this work, we utilized triplet excited nitroarenes to transform linear alkyne topology to bent ketone fragments. The process involves the concurrent insertion of an oxygen atom and the detection of a carbon atom. The effectiveness and broad applicability of this approach were demonstrated through its successful application across diverse substrates (31 examples), compatibility with various functionalities and the modification of bioactive molecules, scalability in large-scale synthesis in continuous flow, and the synthesis of commercially available drug molecules. UV-vis spectroscopic studies unveiled the role of visible light in exciting the nitroarene in its triplet state. Preliminary mechanistic experiments by various kinetic and control experiments elucidated ketene and nitrosoarene as the key intermediates. The deleted carbon is released as CO and CO2 gases.

Keywords

Skeletal editing
Nitroarene photochemistry
Triplet state
Visible light
Cycloaddition reaction
Alkyne
Ketone
Flow-synthesis

Supplementary materials

Title
Description
Actions
Title
Triplet Excited Nitroarene Converts Linear Alkynes to Bent Ketones by Deleting a Carbon Atom
Description
The supplementary information includes all experimental details, including optimization of the synthetic method, synthesis and characterization of all starting materials and products reported in this study, mechanistic studies, and NMR spectra of all products.
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.