Photo-triggered construction of nitrogen-containing aromatic heterocycles under physiological conditions

Clicks: 18
ID: 326286
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #724 of 794 articles by views in phytochemistry letters

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 794 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Precise spatiotemporal control of molecular function is essential for probing biological systems and developing safer therapeutics. Herein, we review photoinducible intramolecular cyclization reactions developed in-house for generating nitrogen-containing aromatic heterocycles. These photoreactions exploit the unique photoreactivity of o-nitrobenzyl oxime ethers, producing iminyl radicals as key intermediates. Notably, these reactions occur under physiological conditions and in cellulo, thereby expanding the design space for photocontrollable molecules in biological environments.
Reference Key
openalex_W7204028509 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Hidenori Okamura, Fumi Nagatsugi
Journal phytochemistry letters
Year 2026
DOI
10.1093/chemle/upag170
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.