Scheidt Research Group
  • Research
    • Complex Synthesis
    • Catalysis
    • Translational Chemistry
  • Publications
  • Group Members
    • Karl Scheidt
    • Current Members
    • Alumni
  • About Us
    • Outreach
  • Contact
Select Page

N-Heterocyclic Carbene-Initiated α-Acylvinyl Anion Reactivity: Additions of α-Hydroxypropargylsilanes to Aldehydes

Methodology

Reynolds, T. E.; Stern, C. A.; Scheidt, K. A.Org. Lett. 2007, 9, 2581-2584.

Highly Stereoselective Formal [3+3] Cycloaddition of Enals and Azomethine Imines Catalyzed by N-Heterocyclic Carbenes

Methodology

Chan, A.; Scheidt, K. A.J. Am. Chem. Soc. 2007, 129, 5334-5335.

Microwave-Assisted Piloty–Robinson Synthesis of 3,4-Disubstitued Pyrroles

Methodology

Milgram, B. C.; Eskildsen, K.; Richter, S. M.; Scheidt, W. R.; Scheidt, K. A.J. Org. Chem. 2007, 72, 3941-3944.

Nucleophilic Acylation of o-Quinone Methides: An Umpolung Strategy for the Synthesis of α-Aryl Ketones and Benzofurans

Methodology

Mattson, A. E.; Scheidt, K. A.J. Am. Chem. Soc. 2007, 129, 4508-4509.

Catalytic Enantioselective Synthesis of Flavanones and Chromanones

Methodology

Biddle, M. A.; Lin, M.; Scheidt, K. A.J. Am. Chem. Soc. 2007, 129, 3830-3831.

Highly Enantioselective Intramolecular Michael Reaction Catalyzed by N-Heterocyclic Carbenes

Methodology

Phillips, E. M.; Wadamoto, M.; Chan, A.; Scheidt, K. A.Angew. Chem. Int. Ed. 2007, 46, 3107-3110.
« Older Entries
Next Entries »
  • Research
  • Complex Synthesis
  • Catalysis
  • Translational Chemistry
  • Publications


  • About Us
  • News
  • Karl Scheidt
  • Current Members
  • Alumni
  • Openings
  • Contact
  • Sitemap
© 2023 Scheidt Research Group