Year |
Citation |
Score |
2022 |
Bang J, Gi S, Lee Y, Tan KL, Lee S. -Selective C-H Functionalization of Arylsilanes Using a Silicon Tethered Directing Group. Organic Letters. PMID 35822845 DOI: 10.1021/acs.orglett.2c02015 |
0.671 |
|
2017 |
Andorfer MC, Grob JE, Hajdin CE, Chael JR, Siuti P, Lilly J, Tan KL, Lewis JC. Understanding Flavin-Dependent Halogenase Reactivity via Substrate Activity Profiling. Acs Catalysis. 7: 1897-1904. PMID 28989809 DOI: 10.1021/Acscatal.6B02707 |
0.541 |
|
2017 |
Keylor MH, Niemeyer ZL, Sigman MS, Tan KL. Inverting Conventional Chemoselectivity in Pd-Catalyzed Amine Arylations with Multiply Halogenated Pyridines. Journal of the American Chemical Society. PMID 28715180 DOI: 10.1021/Jacs.7B05409 |
0.364 |
|
2016 |
Daniels MH, Armand JR, Tan KL. Sequential Regioselective C-H Functionalization of Thiophenes. Organic Letters. PMID 27388746 DOI: 10.1021/Acs.Orglett.6B01205 |
0.379 |
|
2015 |
Liu R, Stephani C, Tan KL, Wang D. Tuning redox potentials of CO2 reduction catalysts for carbon photofixation by Si nanowires Science China Materials. 58: 515-520. DOI: 10.1007/S40843-015-0068-8 |
0.387 |
|
2014 |
Lee S, Blaisdell TP, Kasaplar P, Sun X, Tan KL. Synthesis of 5'-O-DMT-2'-O-TBS Mononucleosides Using an Organic Catalyst. Current Protocols in Nucleic Acid Chemistry / Edited by Serge L. Beaucage ... [Et Al.]. 57: 2.17.1-2.17.11. PMID 24961720 DOI: 10.1002/0471142700.Nc0217S57 |
0.68 |
|
2014 |
Joe CL, Blaisdell TP, Geoghan AF, Tan KL. Distal-selective hydroformylation using scaffolding catalysis. Journal of the American Chemical Society. 136: 8556-9. PMID 24902624 DOI: 10.1021/Ja504247G |
0.392 |
|
2013 |
Lee S, Lee H, Tan KL. Meta-selective C-H functionalization using a nitrile-based directing group and cleavable Si-tether. Journal of the American Chemical Society. 135: 18778-81. PMID 24325399 DOI: 10.1021/Ja4107034 |
0.687 |
|
2013 |
Sun X, Worthy AD, Tan KL. Resolution of terminal 1,2-diols via silyl transfer. The Journal of Organic Chemistry. 78: 10494-9. PMID 24087949 DOI: 10.1021/Jo4012909 |
0.303 |
|
2013 |
Blaisdell TP, Lee S, Kasaplar P, Sun X, Tan KL. Practical silyl protection of ribonucleosides. Organic Letters. 15: 4710-3. PMID 24000770 DOI: 10.1021/Ol402023C |
0.671 |
|
2013 |
Sun X, Lee H, Lee S, Tan KL. Catalyst recognition of cis-1,2-diols enables site-selective functionalization of complex molecules. Nature Chemistry. 5: 790-5. PMID 23965682 DOI: 10.1038/Nchem.1726 |
0.688 |
|
2013 |
Liu R, Stephani C, Han JJ, Tan KL, Wang D. Silicon nanowires show improved performance as photocathode for catalyzed carbon dioxide photofixation. Angewandte Chemie (International Ed. in English). 52: 4225-8. PMID 23471719 DOI: 10.1002/Anie.201210228 |
0.361 |
|
2013 |
Giustra ZX, Tan KL. The efficient desymmetrization of glycerol using scaffolding catalysis. Chemical Communications (Cambridge, England). 49: 4370-2. PMID 22790118 DOI: 10.1039/C2Cc33633B |
0.438 |
|
2012 |
Tan KL, Sun X, Worthy AD. Scaffolding Catalysis: Expanding the Repertoire of Bifunctional Catalysts. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2012: 321-325. PMID 24600164 DOI: 10.1055/S-0031-1290321 |
0.441 |
|
2012 |
Liu R, Yuan G, Joe CL, Lightburn TE, Tan KL, Wang D. Silicon nanowires as photoelectrodes for carbon dioxide fixation. Angewandte Chemie (International Ed. in English). 51: 6709-12. PMID 22615263 DOI: 10.1002/Anie.201202569 |
0.334 |
|
2012 |
Worthy AD, Sun X, Tan KL. Site-selective catalysis: toward a regiodivergent resolution of 1,2-diols. Journal of the American Chemical Society. 134: 7321-4. PMID 22515351 DOI: 10.1021/Ja3027086 |
0.467 |
|
2012 |
Tan KL. Catalysis: Temporary intramolecularity. Nature Chemistry. 4: 253-4. PMID 22437708 DOI: 10.1038/Nchem.1308 |
0.384 |
|
2011 |
Joe CL, Tan KL. Enantioselective hydroformylation of aniline derivatives. The Journal of Organic Chemistry. 76: 7590-6. PMID 21842847 DOI: 10.1021/Jo201328D |
0.358 |
|
2011 |
Sun X, Worthy AD, Tan KL. Scaffolding catalysts: highly enantioselective desymmetrization reactions. Angewandte Chemie (International Ed. in English). 50: 8167-71. PMID 21739552 DOI: 10.1002/Anie.201103470 |
0.471 |
|
2011 |
Lightburn TE, De Paolis OA, Cheng KH, Tan KL. Regioselective hydroformylation of allylic alcohols. Organic Letters. 13: 2686-9. PMID 21504208 DOI: 10.1021/Ol200782D |
0.332 |
|
2011 |
Tan KL. Induced Intramolecularity: An Effective Strategy in Catalysis Acs Catalysis. 1: 877-886. DOI: 10.1021/Cs2002302 |
0.448 |
|
2010 |
Worthy AD, Joe CL, Lightburn TE, Tan KL. Application of a chiral scaffolding ligand in catalytic enantioselective hydroformylation. Journal of the American Chemical Society. 132: 14757-9. PMID 20882977 DOI: 10.1021/Ja107433H |
0.425 |
|
2010 |
Sun X, Frimpong K, Tan KL. Synthesis of quaternary carbon centers via hydroformylation. Journal of the American Chemical Society. 132: 11841-3. PMID 20687551 DOI: 10.1021/Ja1036226 |
0.454 |
|
2010 |
Tan KL, Bergman RG, Ellman JA. ChemInform Abstract: Annulation of Alkenyl-Substituted Heterocycles via Rhodium-Catalyzed Intramolecular C-H Activated Coupling Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200129130 |
0.467 |
|
2009 |
Worthy AD, Gagnon MM, Dombrowski MT, Tan KL. Regioselective hydroformylation of sulfonamides using a scaffolding ligand. Organic Letters. 11: 2764-7. PMID 19489593 DOI: 10.1021/Ol900921E |
0.412 |
|
2008 |
Lightburn TE, Dombrowski MT, Tan KL. Catalytic scaffolding ligands: an efficient strategy for directing reactions. Journal of the American Chemical Society. 130: 9210-1. PMID 18576619 DOI: 10.1021/Ja803011D |
0.419 |
|
2008 |
Lightburn TE, Dombrowski MT, Tan KL. Branch-Selective Hydroformylation by Rh-Scaffolding LigandComplexes Synfacts. 2008: 1080-1080. DOI: 10.1055/S-2008-1078139 |
0.324 |
|
2007 |
Tan KL, Jacobsen EN. Indium-mediated asymmetric allylation of acylhydrazones using a chiral urea catalyst. Angewandte Chemie (International Ed. in English). 46: 1315-7. PMID 17211916 DOI: 10.1002/Anie.200603354 |
0.556 |
|
2007 |
Jacobsen E, Tan K. Asymmetric Allylation of Acylhydrazones Synfacts. 2007: 0435-0435. DOI: 10.1055/S-2007-968345 |
0.553 |
|
2006 |
O’Malley SJ, Tan KL, Watzke A, Bergman RG, Ellman JA. Synthesis of (+)-Lithospermic Acid Synfacts. 2006: 98-98. DOI: 10.1055/S-2005-921780 |
0.431 |
|
2005 |
O'Malley SJ, Tan KL, Watzke A, Bergman RG, Ellman JA. Total synthesis of (+)-lithospermic acid by asymmetric intramolecular alkylation via catalytic C-H bond activation. Journal of the American Chemical Society. 127: 13496-7. PMID 16190703 DOI: 10.1021/Ja052680H |
0.533 |
|
2004 |
Tan KL, Park S, Ellman JA, Bergman RG. Intermolecular coupling of alkenes to heterocycles via C-H bond activation. The Journal of Organic Chemistry. 69: 7329-35. PMID 15471487 DOI: 10.1021/Jo048666P |
0.569 |
|
2003 |
Tan KL, Vasudevan A, Bergman RG, Ellman JA, Souers AJ. Microwave-assisted C-H bond activation: a rapid entry into functionalized heterocycles. Organic Letters. 5: 2131-4. PMID 12790546 DOI: 10.1021/Ol030050J |
0.531 |
|
2003 |
Blum SA, Tan KL, Bergman RG. Application of physical organic methods to the investigation of organometallic reaction mechanisms. The Journal of Organic Chemistry. 68: 4127-37. PMID 12762711 DOI: 10.1021/Jo034198S |
0.646 |
|
2002 |
Tan KL, Bergman RG, Ellman JA. Intermolecular coupling of isomerizable alkenes to heterocycles via rhodium-catalyzed C-H bond activation. Journal of the American Chemical Society. 124: 13964-5. PMID 12440873 DOI: 10.1021/Ja0281129 |
0.582 |
|
2002 |
Tan KL, Bergman RG, Ellman JA. Intermediacy of an N-heterocyclic carbene complex in the catalytic C-H activation of a substituted benzimidazole. Journal of the American Chemical Society. 124: 3202-3. PMID 11916392 DOI: 10.1021/Ja017351D |
0.571 |
|
2001 |
Tan KL, Bergman RG, Ellman JA. Annulation of alkenyl-substituted heterocycles via rhodium-catalyzed intramolecular C-H activated coupling reactions. Journal of the American Chemical Society. 123: 2685-6. PMID 11456947 DOI: 10.1021/ja0058738 |
0.467 |
|
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