| Year |
Citation |
Score |
| 2021 |
Chan YC, Sak MH, Frank SA, Miller SJ. "Tunable and Cooperative Catalysis for Enantioselective Pictet-Spengler Reaction with Varied Nitrogen-Containing Heterocyclic Carboxaldehydes". Angewandte Chemie (International Ed. in English). PMID 34487418 DOI: 10.1002/anie.202109694 |
0.461 |
|
| 2020 |
Struble TJ, Alvarez JC, Brown S, Chytil M, Cisar J, DesJarlais R, Engkvist O, Frank SA, Greve DR, Griffin DJ, Hou X, Johannes JW, Kreatsoulas C, Lahue B, Mathea M, et al. Current and Future Roles of Artificial Intelligence in Medicinal Chemistry Synthesis. Journal of Medicinal Chemistry. PMID 32243158 DOI: 10.1021/Acs.Jmedchem.9B02120 |
0.319 |
|
| 2016 |
May SA, Johnson MD, Buser JY, Campbell AN, Frank SA, Haeberle BD, Hoffman PC, Lambertus GR, McFarland AD, Moher ED, White TD, Hurley DD, Corrigan AP, Gowran O, Kerrigan NG, et al. Development and Manufacturing GMP Scale-Up of a Continuous Ir-Catalyzed Homogeneous Reductive Amination Reaction Organic Process Research & Development. 20: 1870-1898. DOI: 10.1021/Acs.Oprd.6B00148 |
0.434 |
|
| 2014 |
Vaid RK, Boini SK, Alt CA, Spitler JT, Hadden CE, Frank SA, Moher ED. Synthesis of Methyl 7,9-Dimethyl-5-oxo-2,3,4,5-tetrahydro-1 H -benzo[ b ]azepine-1-carboxylate and Its Analogues Synthesis (Germany). 46: 2463-2470. DOI: 10.1055/S-0034-1378279 |
0.457 |
|
| 2014 |
Kocienski P, Frederick MO, Frank SA, Vicenzi JT, LeTourneau ME, Berglund KD, Edward AW, Alt CA. Synthesis of Evacetrapib Synfacts. 10: 673-673. DOI: 10.1055/S-0034-1378239 |
0.488 |
|
| 2014 |
Frederick MO, Frank SA, Vicenzi JT, Letourneau ME, Berglund KD, Edward AW, Alt CA. Development of a hydrogenative reductive amination for the synthesis of evacetrapib: Unexpected benefits of water Organic Process Research and Development. 18: 546-551. DOI: 10.1021/Op500025V |
0.371 |
|
| 2013 |
Kissane MG, Frank SA, Rener GA, Ley CP, Alt CA, Stroud PA, Vaid RK, Boini SK, McKee LA, Vicenzi JT, Stephenson GA. Counterion effects in the preparation of aldehyde-bisulfite adducts Tetrahedron Letters. 54: 6587-6591. DOI: 10.1016/J.Tetlet.2013.09.105 |
0.378 |
|
| 2010 |
Frank SA, Roush WR. ChemInform Abstract: Studies on the Synthesis of (-)-Spinosyn A: Application of the Steric Directing Group Strategy to Transannular Diels-Alder Reactions. Cheminform. 33: no-no. DOI: 10.1002/chin.200247200 |
0.651 |
|
| 2010 |
Frank SA, Mergott DJ, Roush WR. ChemInform Abstract: The Vinylogous Intramolecular Morita-Baylis-Hillman Reaction: Synthesis of Functionalized Cyclopentenes and Cyclohexenes with Trialkylphosphines as Nucleophilic Catalysts. Cheminform. 33: no-no. DOI: 10.1002/chin.200232041 |
0.746 |
|
| 2010 |
Frank SA, Chen H, Kunz RK, Schnaderbeck MJ, Roush WR. ChemInform Abstract: Use of Thallium(I) Ethoxide in Suzuki Cross-Coupling Reactions. Cheminform. 31: no-no. DOI: 10.1002/chin.200046042 |
0.574 |
|
| 2008 |
Yu H, Richey RN, Stout JR, LaPack MA, Gu R, Khau VV, Frank SA, Ott JP, Miller RD, Carr MA, Zhang TY. Development of a pratical synthisis of DPP IV inhibitor LY2497282 Organic Process Research and Development. 12: 218-225. DOI: 10.1021/Op700235C |
0.352 |
|
| 2004 |
Mergott DJ, Frank SA, Roush WR. Total synthesis of (-)-spinosyn A. Proceedings of the National Academy of Sciences of the United States of America. 101: 11955-9. PMID 15173590 DOI: 10.1073/Pnas.0401247101 |
0.751 |
|
| 2002 |
Mergott DJ, Frank SA, Roush WR. Application of the intramolecular vinylogous Morita-Baylis-Hillman reaction toward the synthesis of the spinosyn A tricyclic nucleus. Organic Letters. 4: 3157-60. PMID 12201741 DOI: 10.1021/Ol026540D |
0.759 |
|
| 2002 |
Frank SA, Roush WR. Studies on the synthesis of (-)-spinosyn a: application of the steric directing group strategy to transannular Diels-Alder reactions. The Journal of Organic Chemistry. 67: 4316-24. PMID 12054969 DOI: 10.1021/Jo025580S |
0.69 |
|
| 2002 |
Frank SA, Mergott DJ, Roush WR. The vinylogous intramolecular Morita-Baylis-Hillman reaction: synthesis of functionalized cyclopentenes and cyclohexenes with trialkylphosphines as nucleophilic catalysts. Journal of the American Chemical Society. 124: 2404-5. PMID 11890766 DOI: 10.1021/Ja017123J |
0.756 |
|
| 2000 |
Frank SA, Chen H, Kunz RK, Schnaderbeck MJ, Roush WR. Use of thallium(I) ethoxide in Suzuki cross coupling reactions. Organic Letters. 2: 2691-4. PMID 10990429 DOI: 10.1021/Ol0062446 |
0.728 |
|
| 2000 |
Frank SA, Works AB, Roush WR. Studies on the synthesis of the decahydro-as-indacene ring system of (-)-spinosyn A via transannular Diels-Alder reactions of substituted (E,E,E)-cyclododeca-1,6,8-trienes Canadian Journal of Chemistry. 78: 757-771. DOI: 10.1139/V00-045 |
0.66 |
|
| 1998 |
Udodong UE, Turner WW, Astleford BA, Brown F, Clayton MT, Dunlap SE, Frank SA, Grutsch JL, LaGrandeur LM, Verral DE, Werner JA. Studies on the phosphorylation of LY303366 Tetrahedron Letters. 39: 6115-6118. DOI: 10.1016/S0040-4039(98)01294-5 |
0.327 |
|
| 1997 |
Faul MM, Huff BE, Dunlap SE, Frank SA, Fritz JE, Kaldor SW, LeTourneau ME, Staszak MA, Ward JA, Werner JA, Winneroski LL. Synthesis of 2',3'-dideoxy-3'-hydroxymethylcytidine; A unique antiviral nucleoside Tetrahedron. 53: 8085-8104. DOI: 10.1016/S0040-4020(97)00500-0 |
0.51 |
|
| 1996 |
Werner JA, Cerbone LR, Frank SA, Ward JA, Labib P, Tharp-Taylor RW, Ryan CW. Synthesis of trans-3,4-Dimethyl-4-(3-hydroxyphenyl)piperidine Opioid Antagonists: Application of the Cis-Thermal Elimination of Carbonates to Alkaloid Synthesis. The Journal of Organic Chemistry. 61: 587-597. PMID 11666979 DOI: 10.1021/Jo951403Y |
0.378 |
|
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