Filter By:

Journal Check one or more journals to show results from those journals only.
Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–1 of 1 results
Advanced filters: Author: Jake L. Stymiest Clear advanced filters
  • A new method to convert secondary alcohols in their single mirror image form into tertiary alcohols has been developed. Starting from a single enantiomer of the secondary alcohol, either mirror image form of the tertiary alcohol can be made with very high levels of stereocontrol. A broad range of tertiary alcohols can now be easily made by this method with very high levels of selectivity.

    • Jake L. Stymiest
    • Viktor Bagutski
    • Varinder K. Aggarwal
    Research
    Nature
    Volume: 456, P: 778-782