3 years ago

Highly stereoselective construction of the C2 stereocentre of [small alpha]-tocopherol (vitamin E) by asymmetric addition of Grignard reagents to ketones

Highly stereoselective construction of the C2 stereocentre of [small alpha]-tocopherol (vitamin E) by asymmetric addition of Grignard reagents to ketones
Bartosz Bieszczad, Declan G. Gilheany
Both C2-diastereomers of [small alpha]-tocopherol can be prepared in three ways by asymmetric addition of Grignard reagents to ketones in up to 96 : 4 dr.

Publisher URL: http://feeds.rsc.org/~r/rss/OB/~3/_vOgo8ERJjI/C7OB00751E

DOI: 2017/OB/C7OB00751E

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.