Year |
Citation |
Score |
2021 |
Trost BM, Taft BR, Tracy JS, Stivala CE. Catalytic Asymmetric Synthesis of the Pentacyclic Core of (+)-Citrinadin A. Organic Letters. PMID 34114462 DOI: 10.1021/acs.orglett.1c01389 |
0.372 |
|
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, 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 |
0.443 |
|
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, 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 |
0.447 |
|
2016 |
Trost BM, Masters JT, Taft BR, Lumb JP. Asymmetric synthesis of chiral β-alkynyl carbonyl and sulfonyl derivatives via sequential palladium and copper catalysis. Chemical Science. 7: 6217-6231. PMID 27746892 DOI: 10.1039/C6Sc01724J |
0.707 |
|
2012 |
Lipshutz BH, Isley NA, Moser R, Ghorai S, Leuser H, Taft BR. Rhodium-Catalyzed Asymmetric 1,4-Additions, in Water at Room Temperature, with In-Flask Catalyst Recycling. Advanced Synthesis & Catalysis. 354: 3175-3179. PMID 24659941 DOI: 10.1002/Adsc.201200160 |
0.697 |
|
2012 |
Lipshutz BH, Taft BR, Abela AR, Ghorai S, Krasovskiy A, Duplais C. Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar catalysis. Platinum Metals Review. 56: 62-74. PMID 23555153 DOI: 10.1595/147106712X629761 |
0.752 |
|
2011 |
Trost BM, Taft BR, Masters JT, Lumb JP. A new strategy for the synthesis of chiral β-alkynyl esters via sequential palladium and copper catalysis. Journal of the American Chemical Society. 133: 8502-5. PMID 21557627 DOI: 10.1021/Ja203171X |
0.697 |
|
2011 |
Lipshutz BH, Ghorai S, Leong WW, Taft BR, Krogstad DV. Manipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperature. The Journal of Organic Chemistry. 76: 5061-73. PMID 21539384 DOI: 10.1021/Jo200746Y |
0.593 |
|
2011 |
Trost BM, Taft BR, Masters JT, Lumb J. ChemInform Abstract: A New Strategy for the Synthesis of Chiral β-Alkynyl Esters via Sequential Palladium and Copper Catalysis. Cheminform. 42: no-no. DOI: 10.1002/chin.201145019 |
0.671 |
|
2009 |
Gallagher BD, Taft BR, Lipshutz BH. Asymmetric conjugate reductions of coumarins. A new route to tolterodine and related coumarin derivatives. Organic Letters. 11: 5374-7. PMID 19877705 DOI: 10.1021/Ol9020404 |
0.498 |
|
2009 |
Taft BR, Swift EC, Lipshutz BH. A convenient preparation of di-p-chlorobenzyl azodicarboxylate (DCAD) for mitsunobu couplings Synthesis. 332-334. DOI: 10.1055/S-0028-1083274 |
0.515 |
|
2009 |
Nulwala H, Takizawa K, Odukale A, Khan A, Thibault RJ, Taft BR, Lipshutz BH, Hawker CJ. Synthesis and characterization of isomeric vinyl-1,2,3-triazole materials by azide - Alkyne click chemistry Macromolecules. 42: 6068-6074. DOI: 10.1021/Ma900892H |
0.55 |
|
2008 |
Lipshutz BH, Nihan DM, Vinogradova E, Taft BR, Bosković ZV. Copper + nickel-in-charcoal (Cu-Ni/C): a bimetallic, heterogeneous catalyst for cross-couplings. Organic Letters. 10: 4279-82. PMID 18763793 DOI: 10.1021/Ol801676U |
0.755 |
|
2008 |
Lipshutz BH, Taft BR. Heck couplings at room temperature in nanometer aqueous micelles. Organic Letters. 10: 1329-32. PMID 18335945 DOI: 10.1021/Ol702755G |
0.502 |
|
2007 |
Lipshutz BH, Unger JB, Taft BR. Copper-in-charcoal (Cu/C) promoted diaryl ether formation. Organic Letters. 9: 1089-92. PMID 17305352 DOI: 10.1021/Ol0700409 |
0.715 |
|
2007 |
Lipshutz BH, Lee CT, Taft BR. A conjugate reduction pathway to chiral silanes using CuH Synthesis. 3257-3260. DOI: 10.1055/S-2007-983830 |
0.662 |
|
2007 |
Lipshutz B, Taft B. Cu/C Catalyst for Click Chemistry Synfacts. 2007: 0340-0340. DOI: 10.1055/s-2007-968222 |
0.304 |
|
2006 |
Lipshutz BH, Frieman BA, Lee CT, Lower A, Nihan DM, Taft BR. Microwave-assisted heterogeneous cross-coupling reactions catalyzed by nickel-in-charcoal (Ni/C). Chemistry, An Asian Journal. 1: 417-29. PMID 17441078 DOI: 10.1002/Asia.200600031 |
0.711 |
|
2006 |
Lipshutz BH, Taft BR. Heterogeneous copper-in-charcoal-catalyzed click chemistry. Angewandte Chemie (International Ed. in English). 45: 8235-8. PMID 17111447 DOI: 10.1002/Anie.200603726 |
0.545 |
|
2006 |
Lipshutz BH, Tanaka N, Taft BR, Lee CT. Chiral silanes via asymmetric hydrosilylation with catalytic CuH. Organic Letters. 8: 1963-6. PMID 16671757 DOI: 10.1021/Ol0529593 |
0.678 |
|
2006 |
Lipshutz BH, Butler T, Frieman BA, Kogan V, Lee CT, Lower A, Nihan DM, Taft BR, Tomaso AE. New technologies in catalysis using base metals Pure and Applied Chemistry. 78: 377-384. DOI: 10.1351/Pac200678020377 |
0.691 |
|
2005 |
Frieman BA, Taft BR, Lee CT, Butler T, Lipshutz BH. Nickel-in-charcoal (Ni/C): An efficient heterogeneous catalyst for the construction of C-C, C-N, and C-H bonds Synthesis. 2989-2993. DOI: 10.1055/S-2005-872145 |
0.785 |
|
2004 |
Lipshutz BH, Servesko JM, Taft BR. Asymmetric 1,4-hydrosilylations of alpha,beta-unsaturated esters. Journal of the American Chemical Society. 126: 8352-3. PMID 15237972 DOI: 10.1021/Ja049135L |
0.692 |
|
2004 |
Ball DB, Wood M, Lindsley C, Mollard P, Buzard DJ, Vivian R, Mahoney M, Taft BR. Research, Teaching, and Professional Development at a Comprehensive University Journal of Chemical Education. 81: 1796. DOI: 10.1021/Ed081P1796 |
0.533 |
|
2004 |
Lipshutz BH, Servesko JM, Taft BR. Asymmetric 1,4-Hydrosilylations of α,β-Unsaturated Esters. Cheminform. 35. DOI: 10.1002/chin.200445024 |
0.678 |
|
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