5 years ago

Dienyl esters synthesis: Palladium-catalyzed C–H olefination of electron-deficient alkenes with allenoates

Dienyl esters synthesis: Palladium-catalyzed C–H olefination of electron-deficient alkenes with allenoates
The palladium(II)-catalyzed direct oxidative C–H olefination of readily available N-tosylacrylamides and allenoates for the synthesis of dienyl esters is described. The amide and ester moieties both act as the directing groups for the regio- and the stereo-controlled C–H functionalization/cyclization, which was proved by DFT calculations. Molecular oxygen was used as the terminal oxidant in the approach, rendering the reaction more sustainable.

Publisher URL: www.sciencedirect.com/science

DOI: S0040402017305112

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.