Year |
Citation |
Score |
2024 |
He T, Liang C, Cheng H, Shi S, Huang S. Cathodically Coupled Electrolysis to Access Biheteroaryls. Organic Letters. 26: 607-612. PMID 38206057 DOI: 10.1021/acs.orglett.3c03859 |
0.324 |
|
2019 |
Ramurthy S, Taft BR, Aversa RJ, Barsanti P, Burger MT, Lou Y, Nishiguchi G, Rico A, Setti L, Smith A, Subramanian S, Tamez VNA, Tanner HR, Wan L, Hu C, ... ... Huang S, et al. Design and Discovery of N-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methylphenyl)-2-(trifluoromethyl)isonicotinamide (LXH254)- A selective, efficacious and well-tolerated RAF inhibitor targeting RAS mutant cancers: The path to the clinic. Journal of Medicinal Chemistry. PMID 31059256 DOI: 10.1021/Acs.Jmedchem.9B00161 |
0.639 |
|
2018 |
Feng Q, Chen D, Hong M, Wang F, Huang S. Phenyliodine(III) Bis(trifluoroacetate) (PIFA)-Mediated Synthesis of Aryl Sulfides in Water. The Journal of Organic Chemistry. PMID 29664643 DOI: 10.1021/acs.joc.8b00435 |
0.316 |
|
2017 |
Nishiguchi GA, Rico A, Tanner HR, Aversa RJ, Taft BR, Subramanian S, Setti L, Burger MT, Wan L, Tamez VNA, Smith A, Lou Y, Barsanti PA, Appleton BA, Mamo M, ... ... Huang S, et al. Design and Discovery of N-(2-methyl-5'-morpholino-6'-((tetrahydro-2H-pyran-4-yl)oxy)-[3,3'-bipyridin]-5-yl)-3-(trifluoromethyl)benzamide (RAF709): A potent, selective and efficacious RAF inhibitor targeting RAS mutant cancers. Journal of Medicinal Chemistry. PMID 28557458 DOI: 10.1021/Acs.Jmedchem.6B01862 |
0.642 |
|
2016 |
Nishikata T, Abela AR, Huang S, Lipshutz BH. Cationic Pd(II)-catalyzed C-H activation/cross-coupling reactions at room temperature: synthetic and mechanistic studies. Beilstein Journal of Organic Chemistry. 12: 1040-64. PMID 27340491 DOI: 10.3762/Bjoc.12.99 |
0.731 |
|
2012 |
Lipshutz BH, Huang S, Leong WW, Zhong G, Isley NA. C-C bond formation via copper-catalyzed conjugate addition reactions to enones in water at room temperature. Journal of the American Chemical Society. 134: 19985-8. PMID 23190029 DOI: 10.1021/Ja309409E |
0.573 |
|
2010 |
Huang S, Petersen TB, Lipshutz BH. Total synthesis of (+)-korupensamine B via an atropselective intermolecular biaryl coupling. Journal of the American Chemical Society. 132: 14021-3. PMID 20849111 DOI: 10.1021/Ja1065202 |
0.696 |
|
2010 |
Nishikata T, Abela AR, Huang S, Lipshutz BH. Cationic palladium(II) catalysis: C-H activation/Suzuki-Miyaura couplings at room temperature. Journal of the American Chemical Society. 132: 4978-9. PMID 20307066 DOI: 10.1021/Ja910973A |
0.724 |
|
2010 |
Lipshutz B, Huang S, Petersen T. Atropselective Biaryl Coupling in the Synthesis of (+)-Korupensamine B Synfacts. 2010: 1395-1395. DOI: 10.1055/s-0030-1258894 |
0.714 |
|
2010 |
Huang S, Voigtritter KR, Unger JB, Lipshutz BH. Asymmetric CuH-catalyzed 1,4-reductions in water at room temperature Synlett. 2041-2044. DOI: 10.1055/S-0030-1258540 |
0.665 |
|
2009 |
Lee C, Huang S, Lipshutz B. Copper-in-Charcoal-Catalyzed, Tandem One-Pot Diazo Transfer-Click Reactions Advanced Synthesis & Catalysis. 351: 3139-3142. DOI: 10.1002/Adsc.200900604 |
0.629 |
|
2007 |
Huang S, Lin R, Yu Y, Lu Y, Connolly PJ, Chiu G, Li S, Emanuel SL, Middleton SA. Synthesis of 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitor. Bioorganic & Medicinal Chemistry Letters. 17: 1243-5. PMID 17234412 DOI: 10.1002/chin.200729132 |
0.308 |
|
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