Solvent-controlled selective synthesis of biphenols and quinones via oxidative coupling of phenols.
Clicks: 341
ID: 263122
2017
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
Steady Performance
81.5
/100
341 views
232 readers
Trending
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #29 of 184 articles by views in Chemical communications (Cambridge, England)
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 184 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
A regioselective synthesis of unsymmetrical and symmetrical biphenols and binaphthols via oxidative coupling of phenols or naphthols in the presence of KSO in CFCOOH under ambient conditions is described. Interestingly, the 1 : 1 ratio of HO and CHCN solvent mixtures at 80 °C instead of CFCOOH provided substituted unsymmetrical quinones. A gram-scale synthesis of biphenols and binaphthols was demonstrated.
| Reference Key |
more2017solventcontrolledchemical
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | More, Nagnath Yadav;Jeganmohan, Masilamani; |
| Journal | Chemical communications (Cambridge, England) |
| Year | 2017 |
| DOI |
10.1039/c7cc04829g
|
| URL | |
| Keywords |
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.