skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


  • Home
  • Search Results
  • Page 1 of 1

Search for: All records

Creators/Authors contains: "Troya, Diego"

Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher. Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?

Some links on this page may take you to non-federal websites. Their policies may differ from this site.

  1. ; ; ; (, Polymer Chemistry)
    We report highkp(macro)monomer structures for use in grafting-through ring-opening metathesis polymerization to make linear and bottlebrush polymers. 
    more » « less
    Full Text Available 
  2. ; ; ; (, Macromolecules)
    Full Text Available 
  3. ; ; ; ; ; ; (, Macromolecules)
    Full Text Available 
  4. ; ; (, The Journal of Physical Chemistry B)
    Full Text Available 
  5. ; ; ; (, Angewandte Chemie International Edition)
    Abstract We report herein a Cu‐catalyzed regio‐, diastereo‐ and enantioselective acylboration of 1,3‐butadienylboronate with acyl fluorides. Under the developed conditions, the reactions provide (Z)‐β,γ‐unsaturated ketones bearing an α‐tertiary stereocenter with highZ‐selectivity and excellent enantioselectivities. While direct access to highly enantioenrichedE‐isomers was not successful, we showed that such molecules can be synthesized with excellentE‐selectivity and optical purities via Pd‐catalyzed alkene isomerization from the correspondingZ‐isomers. The orthogonal chemical reactivities of the functional groups embedded in the ketone products allow for diverse chemoselective transformations, which provides a valuable platform for further derivatization. 
    more » « less
  6. ; ; ; ; (, Macromolecules)
    null (Ed.)
    Full Text Available 
  7. ; ; ; (, Macromolecules)
    Full Text Available 
  8. ; ; ; ; ; ; ; ; ; ; et al (, Journal of the American Chemical Society)
    null (Ed.)
    Full Text Available 
  9. ; ; ; (, The Journal of Physical Chemistry B)
    Full Text Available 
  10. ; ; ; ; ; (, ACS Energy Letters)