3 years ago

A chiral multidentate salan-supported heterobimetallic catalyst for asymmetric Friedel-Crafts reaction

A chiral multidentate salan-supported heterobimetallic catalyst for asymmetric Friedel-Crafts reaction
A new hydroxymethyl-pendant salan (3) containing a chiral backbone and an extra O4 cavity has been prepared through a facile one-pot procedure. The ligand has been characterized by ESI-MS, elemental analysis and 2D NMR techniques. To continue our previous work on the catalytically asymmetric F-C reactions using multimetallic complexes involving salan-type ligands, we investigated the applicability of 3 for both asymmetric Henry and F-C reactions, in comparison with previously reported results using salans 1 and 2. It was revealed that although 3 was not a suitable ligand for homometallic copper-catalyzed Henry reaction, it was effective for the hetereobimetallic Cu/Zn-catalyzed asymmetric F-C reaction, affording desired alkylated product with good yield and moderate enantiomeric excess (ee), after screening of various catalyst combinations.

Publisher URL: www.sciencedirect.com/science

DOI: S1387700316304427

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.