Inventor

SCHEIDT KARL A

US33 patents

⚠️ This page may combine multiple inventors who share the name “SCHEIDT KARL A”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

SCHEIDT KARL A

UNIV NORTHWESTERN

Inhibition of cancer cell motility

Catalytic enantioselective synthesis of 2-aryl chromenes and related phosphoramidite ligands and catalyst compounds

Inhibition of cancer cell motility

Catalytic enantioselective synthesis of 2-aryl chromenes and related phosphoramidite ligands and catalyst compounds

Inhibition of cancer cell motility

Catalytic enantioselective synthesis of 2-aryl chromenes and related phosphoramidite ligands and catalyst compounds

Catalytic enantioselective synthesis of 2-aryl chromenes and related phosphoramidite ligands and catalyst compounds

Enantioselective syntheses of heteroyohimbine natural product intermediates

Enantioselective syntheses of heteroyohimbine natural product intermediates

Azolium metal-organic frameworks

Inhibition and treatment of prostate cancer metastasis

Catalysts and methods for enantioselective conjugate additions of amines to unsaturated electrophiles

Substituted pyrrolo[2,3-d]pyrimidines for the treatment of cancer and proliferative disorders

Enantioselective N-heterocyclic carbene-catalyzed annulation reactions with imidazolidinones

7-membered fused heterocycles and methods of their synthesis

N-heterocyclic carbene-catalyzed synthesis of 2-aryl indoles

Chiral imidazolium salts for asymmetric catalysis

3-methylideneoxan-4-one compounds and substituted derivatives thereof as inhibitors of telomerase

Agents that target telomerase reverse transcriptase (TERT) for treating cancer and sensitizing cancer cells to genotoxic therapy

Substituted fused pyrrolo-diazepinones and uses thereof

Substituted fused pyrrolo-diazepinones and uses thereof

3-methylideneoxan-4-one compounds and substituted derivates thereof as inhibitors of telomerase

Catalysts and methods for enantioselective conjugate addition of amines to unsaturated electrophiles

Substituted dihydrobenzoxazinones, dihydroquinolones, and methods of their use and synthesis

Beta-carbolines as positive allosteric modulators of the human serotonin receptor 2C (5-HT2C)

Substituted chromanes, analogs thereof, and methods of use and synthesis

Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions

Substituted chromanes, analogs thereof, and methods of use and synthesis

3-arylindazoles as selective MEK4 inhibitors

Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions

Substituted tetrahydropyranoindoles, derivatives thereof, and their methods of synthesis and use

BERGAN RAYMOND C

Inhibition and treatment of prostate cancer metastasis

SCHEIDT KARL A

Azolium metal-organic frameworks