Exploring Low-Cost Methods for BEpin Borylation of Aryl Iodides using Nickel catalysts
Clicks: 1
ID: 316323
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.
Reader Engagement
0.0
/100
1 views
0 readers
AI Quality Assessment
Not analyzed
Readership in this journal
Ranked #775 of 788 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 788 in total.
Mint this article as an NFT
Not yet mintedCreate 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 Herein, we present our investigation into a low-cost Miyaura borylation method for the formation of Ar-BEpin compounds. The method described occurs at room temperature, is catalysed by nickel, and produces boronic esters, which are more stable than the boronic acid or Bpin ester equivalents. This work also examines the rates of the two borylating agents, B2Pin2 and B2Epin2, at room temperature.
| Reference Key |
openalex_W7163805850
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Jiashen Tan, Daven Foster, George; id_orcid 0000-0001-8755-3596 Koutsantonis, Reto Dorta, Scott Stewart |
| Journal | phytochemistry letters |
| Year | 2026 |
| DOI |
10.1093/chemle/upag107
|
| URL | |
| 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.