Powered by OpenAIRE graph
Found an issue? Give us feedback
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ Organic & Biomolecul...arrow_drop_down
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
Lirias
Article . 2020
Data sources: Lirias
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Organic & Biomolecular Chemistry
Article . 2020 . Peer-reviewed
License: Royal Society of Chemistry Licence to Publish
Data sources: Crossref
versions View all 4 versions
addClaim

Aldehydes: magnificent acyl equivalents for direct acylation

Authors: Kumar, Prashant; Dutta, Sriparna; Kumar, Sandeep; Bahadur, Vijay; van der Eycken, Erik V.; Vimaleswaran, Karani Santhanarishnan; Parmar, Virinder S.; +1 Authors

Aldehydes: magnificent acyl equivalents for direct acylation

Abstract

This review sheds light on the use of aldehydes in the selective acylation of arene, heteroarene and alkyl (sp3, sp2and sp) C–H bonds by proficient utilization of the C–H activation strategy.

Countries
Russian Federation, Belgium
Keywords

Novel molecules, Reaction steps, Acylation, C-H ACTIVATION, Chemistry, Organic, AROMATIC-ALDEHYDES, 0305 Organic Chemistry, Bioactive compounds, GRIGNARD-REAGENTS, Acylated products, DIRECT ACCESS, 3404 Medicinal and biomolecular chemistry, CARBOXYLIC-ACIDS, Aldehydes, Science & Technology, 0304 Medicinal and Biomolecular Chemistry, Activation analysis, Title compounds, PALLADIUM-CATALYZED ACYLATION, Organic Chemistry, Mechanistic aspects, Ketones, Chemical activation, 540, Chemistry, DIRECT N-ACYLATION, C-h activation, Green chemistry, Synthesis (chemical), Physical Sciences, VISIBLE-LIGHT PHOTOREDOX, 3405 Organic chemistry, METAL-FREE, OXIDATIVE ACYLATION

  • BIP!
    Impact byBIP!
    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    31
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Average
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
31
Top 10%
Average
Top 10%
Green
bronze