One-step synthesis of C -alkylated tetrazoles via coupling of ethers with C -sulfonylated tetrazole promoted by a photoexcited aryl ketone

Clicks: 36
ID: 329151
2026
Free PDF
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 820 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 820 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
Sign in to mint
Abstract
Abstract A one-step synthesis of C-alkylated tetrazoles was achieved by coupling of ethers with 1-phenyl-5-methylsulfonyl-1H-tetrazole as the introducing tetrazole source in the presence of photoexcited benzophenone as the C(sp3)–H bond-cleaving agent. The present transformation proceeds via generation of an α-oxy carbon radical derived from the starting ether and can be carried out at ambient temperature even in protic solvents such as alcohol and water.
Reference Key
openalex_W7213607103 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Reika Nakamura, Toshihiro Murafuji, Shin Kamijo
Are you one of these authors? Claim your profile
Journal phytochemistry letters
Year 2026
DOI
10.1093/chemle/upag188
URL
https://doi.org/10.1093/chemle/upag188
Keywords Keywords not found

Citations

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

Comments

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