| Year |
Citation |
Score |
| 2019 |
Hackel T, McGrath NA. Tris(pentafluorophenyl)borane-Catalyzed Reactions Using Silanes. Molecules (Basel, Switzerland). 24. PMID 30691072 DOI: 10.3390/Molecules24030432 |
0.312 |
|
| 2016 |
Vasta JD, Choudhary A, Jensen KH, McGrath NA, Raines RT. Prolyl 4-Hydroxylase: Substrate Isosteres in Which an (E)- or (Z)-Alkene Replaces the Prolyl Peptide Bond. Biochemistry. PMID 28001367 DOI: 10.1021/Acs.Biochem.6B00976 |
0.712 |
|
| 2016 |
Lucas KM, Kleman AF, Sadergaski LR, Jolly CL, Bollinger BS, Mackesey BL, McGrath NA. Versatile, mild, and selective reduction of various carbonyl groups using an electron-deficient boron catalyst. Organic & Biomolecular Chemistry. PMID 27005847 DOI: 10.1039/C6Ob00127K |
0.334 |
|
| 2015 |
Andersen KA, Aronoff MR, McGrath NA, Raines RT. Diazo groups endure metabolism and enable chemoselectivity in cellulo. Journal of the American Chemical Society. 137: 2412-5. PMID 25658416 DOI: 10.1021/Ja5095815 |
0.704 |
|
| 2015 |
McGrath NA, Andersen KA, Davis AK, Lomax JE, Raines RT. Diazo compounds for the bioreversible esterification of proteins. Chemical Science (Royal Society of Chemistry : 2010). 6: 752-755. PMID 25544883 DOI: 10.1039/C4Sc01768D |
0.708 |
|
| 2013 |
Marshall CJ, Agarwal N, Kalia J, Grosskopf VA, McGrath NA, Abbott NL, Raines RT, Shusta EV. Facile chemical functionalization of proteins through intein-linked yeast display. Bioconjugate Chemistry. 24: 1634-44. PMID 23924245 DOI: 10.1021/Bc4002618 |
0.696 |
|
| 2012 |
McGrath NA, Raines RT. Diazo Compounds as Highly Tunable Reactants in 1,3-Dipolar Cycloaddition Reactions with Cycloalkynes(). Chemical Science (Royal Society of Chemistry : 2010). 3: 3237-3240. PMID 23227302 DOI: 10.1039/C2Sc20806G |
0.515 |
|
| 2012 |
Palte MJ, Davis AK, McGrath NA, Spiegel CA, Raines RT. Ribonucleoside 3'-phosphates as pro-moieties for an orally administered drug. Chemmedchem. 7: 1361-4. PMID 22807330 DOI: 10.1002/Cmdc.201200243 |
0.736 |
|
| 2012 |
Ellis GA, McGrath NA, Palte MJ, Raines RT. Ribonuclease-Activated Cancer Prodrug. Acs Medicinal Chemistry Letters. 3: 268-272. PMID 22611478 DOI: 10.1021/Ml2002554 |
0.712 |
|
| 2012 |
Palte MJ, Davis AKF, McGrath NA, Spiegel CA, Raines RT. Inside Cover: Ribonucleoside 3′-Phosphates as Pro-Moieties for an Orally Administered Drug (ChemMedChem 8/2012) Chemmedchem. 7: 1302-1302. DOI: 10.1002/Cmdc.201290036 |
0.459 |
|
| 2011 |
McGrath NA, Raines RT. Chemoselectivity in chemical biology: acyl transfer reactions with sulfur and selenium. Accounts of Chemical Research. 44: 752-61. PMID 21639109 DOI: 10.1021/Ar200081S |
0.57 |
|
| 2011 |
McGrath NA, Binner JR, Markopoulos G, Brichacek M, Njardarson JT. An efficient oxidative dearomatization-radical cyclization approach to symmetrically substituted bicyclic guttiferone natural products. Chemical Communications (Cambridge, England). 47: 209-11. PMID 20607196 DOI: 10.1039/C0Cc01419B |
0.735 |
|
| 2010 |
McGrath NA, Brichacek M, Njardarson JT. A graphical journey of innovative organic architectures that have improved our lives Journal of Chemical Education. 87: 1348-1349. DOI: 10.1021/Ed1003806 |
0.71 |
|
| 2010 |
Brichacek M, Batory LA, McGrath NA, Njardarson JT. The strategic marriage of method and motif. Total synthesis of varitriol Tetrahedron. 66: 4832-4840. DOI: 10.1016/J.Tet.2010.03.038 |
0.664 |
|
| 2009 |
McGrath NA, Bartlett ES, Sittihan S, Njardarson JT. A concise ring-expansion route to the compact core of platensimycin. Angewandte Chemie (International Ed. in English). 48: 8543-6. PMID 19798708 DOI: 10.1002/Anie.200903347 |
0.668 |
|
| 2008 |
McGrath NA, Lee CA, Araki H, Brichacek M, Njardarson JT. An efficient substrate-controlled approach towards hypoestoxide, a member of a family of diterpenoid natural products with an inside-out [9.3.1]bicyclic core. Angewandte Chemie (International Ed. in English). 47: 9450-3. PMID 18979485 DOI: 10.1002/Anie.200804237 |
0.731 |
|
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