Issue 79, 2023

Photogenerated donor–donor diazo compounds enable facile access to spirocyclopropanes

Abstract

Prompted by the increasing interest in strained hydrocarbons as potential drug candidates, we developed a simple and efficient photochemical protocol for (spiro)cyclopropanes from bench stable tosylhydrazones and electron poor olefins. This two-step one-pot transformation proceeds by (3+2)-cycloaddition of in situ formed donor–donor diazo compounds, followed by nitrogen extrusion of the Δ1-pyrazoline intermediates. Notably, kinetic analysis enabled the isolation of intermediary spiro-heterocycles.

Graphical abstract: Photogenerated donor–donor diazo compounds enable facile access to spirocyclopropanes

Supplementary files

Article information

Article type
Communication
Submitted
25 jul 2023
Accepted
08 set 2023
First published
11 set 2023

Chem. Commun., 2023,59, 11835-11838

Photogenerated donor–donor diazo compounds enable facile access to spirocyclopropanes

V. George and B. König, Chem. Commun., 2023, 59, 11835 DOI: 10.1039/D3CC03581F

To request permission to reproduce material from this article, 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 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