Year |
Citation |
Score |
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Organic & Inorganic Au. 3: 321-327. PMID 38075448 DOI: 10.1021/acsorginorgau.3c00050 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Central Science. 9: 1846-1852. PMID 37901169 DOI: 10.1021/acscentsci.3c01136 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Medicinal Chemistry Letters. 14: 1311-1317. PMID 37849544 DOI: 10.1021/acsmedchemlett.3c00412 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Biochemistry. PMID 37772735 DOI: 10.1021/acs.biochem.3c00495 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Organic Letters. PMID 37772728 DOI: 10.1021/acs.orglett.3c03103 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Journal of Medicinal Chemistry. PMID 37772719 DOI: 10.1021/acs.jmedchem.3c01704 |
0.682 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. The Journal of Organic Chemistry. PMID 37772717 DOI: 10.1021/acs.joc.3c02082 |
0.682 |
|
2018 |
Metsänen TT, Lexa KW, Santiago CB, Chung CK, Xu Y, Liu Z, Humphrey GR, Ruck RT, Sherer EC, Sigman MS. Combining traditional 2D and modern physical organic-derived descriptors to predict enhanced enantioselectivity for the key aza-Michael conjugate addition in the synthesis of Prevymis™ (letermovir). Chemical Science. 9: 6922-6927. PMID 30210766 DOI: 10.1039/C8Sc02089B |
0.495 |
|
2017 |
Ji Y, Li H, Hyde AM, Chen Q, Belyk KM, Lexa KW, Yin J, Sherer EC, Williamson RT, Brunskill A, Ren S, Campeau LC, Davies IW, Ruck RT. A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions. Chemical Science. 8: 2841-2851. PMID 28553522 DOI: 10.1039/C6Sc05472B |
0.438 |
|
2017 |
Ashley ER, Sherer EC, Pio B, Orr RK, Ruck RT. Ruthenium-Catalyzed Dynamic Kinetic Resolution Asymmetric Transfer Hydrogenation of β-Chromanones by an Elimination-Induced Racemization Mechanism Acs Catalysis. 7: 1446-1451. DOI: 10.1021/Acscatal.6B03191 |
0.647 |
|
2013 |
Bassan E, Ruck RT, Dienemann E, Emerson KM, Humphrey GR, Raheem IT, Tschaen DM, Vickery TP, Wood HB, Yasuda N. Merck's Reaction Review Policy: An Exercise in Process Safety Organic Process Research and Development. 17: 1611-1616. DOI: 10.1021/op4002033 |
0.603 |
|
2005 |
Blum SA, Rivera VA, Ruck RT, Michael FE, Bergman RG. Synthetic and Mechanistic Studies of Strained Heterocycle Opening Reactions Mediated by Zirconium(IV) Imido Complexes. Organometallics. 24: 1647-1659. PMID 16508693 DOI: 10.1021/Om049105R |
0.391 |
|
2004 |
Ruck RT, Bergman RG. Reactions of Imines with Azazirconacyclobutenes and Generation of Electron-Deficient Imidozirconocene Complexes. Organometallics. 23: 2231-2233. PMID 16508694 DOI: 10.1021/Om0497994 |
0.35 |
|
2004 |
Ruck RT, Bergman RG. Zirconium-mediated conversion of amides to nitriles: a surprising additive effect. Angewandte Chemie (International Ed. in English). 43: 5375-7. PMID 15468091 DOI: 10.1002/Anie.200461064 |
0.42 |
|
2004 |
Ruck RT, Zuckerman RL, Krska SW, Bergman RG. Carboamination: additions of imine C=N bonds across alkynes catalyzed by imidozirconium complexes. Angewandte Chemie (International Ed. in English). 43: 5372-4. PMID 15468090 DOI: 10.1002/Anie.200461063 |
0.403 |
|
2003 |
Ruck RT, Jacobsen EN. Asymmetric hetero-ene reactions of trimethylsilyl enol ethers catalyzed by tridentate Schiff base chromium(III) complexes. Angewandte Chemie (International Ed. in English). 42: 4771-4. PMID 14562344 DOI: 10.1002/Anie.200351591 |
0.516 |
|
2002 |
Ruck RT, Jacobsen EN. Asymmetric catalysis of hetero-ene reactions with tridentate Schiff base chromium(III) complexes. Journal of the American Chemical Society. 124: 2882-3. PMID 11902873 DOI: 10.1021/Ja025588J |
0.503 |
|
Low-probability matches (unlikely to be authored by this person) |
2020 |
Ruck RT. Eric Jacobsen and Gender Diversity in Organic Chemistry Advanced Synthesis & Catalysis. 362: 285-286. DOI: 10.1002/ADSC.201901110 |
0.275 |
|
2017 |
Chung CK, Liu Z, Lexa K, Andreani T, Xu Y, Ji Y, DiRocco DA, Humphrey GR, Ruck RT. Asymmetric Hydrogen Bonding Catalysis for the Synthesis of Dihydroquinazoline-containing Antiviral, Letermovir. Journal of the American Chemical Society. PMID 28737937 DOI: 10.1021/Jacs.7B05806 |
0.231 |
|
2018 |
Friedfeld MR, Zhong H, Ruck RT, Shevlin M, Chirik PJ. Cobalt-catalyzed asymmetric hydrogenation of enamides enabled by single-electron reduction. Science (New York, N.Y.). 360: 888-893. PMID 29798879 DOI: 10.1126/Science.Aar6117 |
0.206 |
|
2019 |
Vanable EP, Kennemur JL, Joyce LA, Ruck RT, Schultz DM, Hull KL. Rhodium-Catalyzed Asymmetric Hydroamination of Allyl Amines. Journal of the American Chemical Society. PMID 30614700 DOI: 10.1021/Jacs.8B09811 |
0.201 |
|
2019 |
Daponte JA, Guo Y, Ruck RT, Hein JE. Using an Automated Monitoring Platform for Investigations of Biphasic Reactions Acs Catalysis. 9: 11484-11491. DOI: 10.1021/Acscatal.9B03953 |
0.199 |
|
2008 |
Ruck RT, Huffman MA, Kim MM, Shevlin M, Kandur WV, Davies IW. ChemInform Abstract: Palladium-Catalyzed Tandem Heck Reaction/C-H Functionalization - Preparation of Spiro-Indan Oxindoles. Cheminform. 39. DOI: 10.1002/CHIN.200841027 |
0.188 |
|
2017 |
DiRocco DA, Ji Y, Sherer EC, Klapars A, Reibarkh M, Dropinski J, Mathew R, Maligres P, Hyde AM, Limanto J, Brunskill A, Ruck RT, Campeau LC, Davies IW. A multifunctional catalyst that stereoselectively assembles prodrugs. Science (New York, N.Y.). 356: 426-430. PMID 28450641 DOI: 10.1126/Science.Aam7936 |
0.188 |
|
2021 |
Klapars A, Chung JYL, Limanto J, Calabria R, Campeau LC, Campos KR, Chen W, Dalby SM, Davis TA, DiRocco DA, Hyde AM, Kassim AM, Larsen MU, Liu G, Maligres PE, ... ... Ruck RT, et al. Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036. PMID 34276931 DOI: 10.1039/d1sc01978c |
0.181 |
|
2021 |
Klapars A, Chung JYL, Limanto J, Calabria R, Campeau LC, Campos KR, Chen W, Dalby SM, Davis TA, DiRocco DA, Hyde AM, Kassim AM, Larsen MU, Liu G, Maligres PE, ... ... Ruck RT, et al. Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036. PMID 34276931 DOI: 10.1039/d1sc01978c |
0.181 |
|
2008 |
Ruck RT, Huffman MA, Kim MM, Shevlin M, Kandur WV, Davies IW. Palladium-catalyzed tandem Heck reaction/C-H functionalization--preparation of spiro-indane-oxindoles. Angewandte Chemie (International Ed. in English). 47: 4711-4. PMID 18491340 DOI: 10.1002/anie.200800549 |
0.181 |
|
2016 |
Basu K, Poirier M, Ruck RT. Solution to the C3-Arylation of Indazoles: Development of a Scalable Method. Organic Letters. PMID 27336404 DOI: 10.1021/acs.orglett.6b01456 |
0.179 |
|
2012 |
Bellomo A, Celebi-Olcum N, Bu X, Rivera N, Ruck RT, Welch CJ, Houk KN, Dreher SD. Rapid catalyst identification for the synthesis of the pyrimidinone core of HIV integrase inhibitors. Angewandte Chemie (International Ed. in English). 51: 6912-5. PMID 22689502 DOI: 10.1002/Anie.201201720 |
0.171 |
|
2022 |
McIntosh JA, Liu Z, Andresen BM, Marzijarani NS, Moore JC, Marshall NM, Borra-Garske M, Obligacion JV, Fier PS, Peng F, Forstater JH, Winston MS, An C, Chang W, Lim J, ... ... Ruck RT, et al. A kinase-cGAS cascade to synthesize a therapeutic STING activator. Nature. 603: 439-444. PMID 35296845 DOI: 10.1038/s41586-022-04422-9 |
0.133 |
|
2016 |
Christensen M, Nolting A, Shevlin M, Weisel M, Maligres PE, Lee J, Orr RK, Plummer CW, Tudge MT, Campeau LC, Ruck RT. Enantioselective Synthesis of α-Methyl-β-Cyclopropyldihydrocinnamates. The Journal of Organic Chemistry. PMID 26743694 DOI: 10.1021/acs.joc.5b02296 |
0.132 |
|
1998 |
Ruck RT, Jones M. Solvent perturbs the reactivity of tert-butylcarbene Tetrahedron Letters. 39: 2277-2280. DOI: 10.1016/S0040-4039(98)00291-3 |
0.132 |
|
2019 |
Ruck RT, Faul MM. Gender Diversity in Process Chemistry Organic Process Research & Development. 23: 109-113. DOI: 10.1021/ACS.OPRD.8B00378 |
0.121 |
|
2018 |
Twilton J, Christensen M, DiRocco DA, Ruck RT, Davies IW, MacMillan DW. Selective Hydrogen Atom Abstraction via Induced Bond Polarization: The Direct -Arylation of Alcohols via Photoredox, HAT and Nickel Catalysis. Angewandte Chemie (International Ed. in English). PMID 29490112 DOI: 10.1002/Anie.201800749 |
0.117 |
|
2018 |
Orr RK, McCabe Dunn JM, Nolting A, Hyde AM, Ashley ER, Leone J, Sirota E, Jurica JA, Gibson A, Wise C, Oliver S, Ruck RT. New reactions and processes for the efficient synthesis of a HCV NS5b prodrug Green Chemistry. 20: 2519-2525. DOI: 10.1039/C8GC00102B |
0.116 |
|
2017 |
Xu F, Zhong YL, Li H, Qi J, Desmond R, Song ZJ, Park J, Wang T, Truppo M, Humphrey GR, Ruck RT. Asymmetric Synthesis of Functionalized trans-Cyclopropoxy Building Block for Grazoprevir. Organic Letters. PMID 29052413 DOI: 10.1021/acs.orglett.7b02867 |
0.115 |
|
2017 |
McCabe Dunn JM, Reibarkh M, Sherer EC, Orr RK, Ruck RT, Simmons B, Bellomo A. The protecting-group free selective 3'-functionalization of nucleosides. Chemical Science. 8: 2804-2810. PMID 28553517 DOI: 10.1039/C6Sc05081F |
0.11 |
|
2016 |
Orr R, Campeau L, Chobanian H, McCabe Dunn J, Pio B, Plummer C, Nolting A, Ruck R. A Modular Synthesis of 2-Alkyl- and 2-Arylchromans via a Three-Step Sequence Synthesis. 49: 657-666. DOI: 10.1055/s-0036-1588075 |
0.099 |
|
2011 |
Mangion IK, Ruck RT, Rivera N, Huffman MA, Shevlin M. A concise synthesis of a β-lactamase inhibitor. Organic Letters. 13: 5480-3. PMID 21916523 DOI: 10.1021/ol202195n |
0.094 |
|
2016 |
Chung CK, Cleator E, Dumas AM, Hicks JD, Humphrey GR, Maligres PE, Nolting AF, Rivera N, Ruck RT, Shevlin M. A Synthesis of a Spirocyclic Macrocyclic Protease Inhibitor for the Treatment of Hepatitis C. Organic Letters. PMID 26950496 DOI: 10.1021/acs.orglett.6b00331 |
0.09 |
|
2008 |
Kim MM, Ruck RT, Zhao D, Huffman MA. Green iodination of pyrazoles with iodine/hydrogen peroxide in water Tetrahedron Letters. 49: 4026-4028. DOI: 10.1016/j.tetlet.2008.04.082 |
0.088 |
|
2016 |
Neelamkavil SF, Agrawal S, Bara T, Bennett C, Bhat S, Biswas D, Brockunier L, Buist N, Burnette D, Cartwright M, Chackalamannil S, Chase R, Chelliah M, Chen A, Clasby M, ... ... Ruck RT, et al. Discovery of MK-8831, A Novel Spiro-Proline Macrocycle as a Pan-Genotypic HCV-NS3/4a Protease Inhibitor. Acs Medicinal Chemistry Letters. 7: 111-6. PMID 26819676 DOI: 10.1021/Acsmedchemlett.5B00425 |
0.068 |
|
2017 |
Boga SB, Christensen M, Perrotto N, Krska SW, Dreher S, Tudge MT, Ashley ER, Poirier M, Reibarkh M, Liu Y, Streckfuss E, Campeau L, Ruck RT, Davies IW, Vachal P. Selective functionalization of complex heterocycles via an automated strong base screening platform Reaction Chemistry & Engineering. 2: 446-450. DOI: 10.1039/C7Re00057J |
0.06 |
|
2020 |
Ren H, Maloney KM, Basu K, Di Maso MJ, Humphrey G, Peng F, Desmond R, Otte DAL, Alwdi E, Liu W, Zhang SW, Song S, Arvary RA, Zompa MA, Lehnherr D, ... ... Ruck RT, et al. Development of a Green & Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 1: Introduction and Process Overview Org. Process Res. Dev.. DOI: 10.1021/acs.oprd.0c00248 |
0.053 |
|
2018 |
Yu W, Tong L, Selyutin O, Chen L, Hu B, Zhong B, Hao J, Ji T, Zan S, Yin J, Ruck RT, Curry S, McMonagle P, Agrawal S, Rokosz L, et al. The Discovery of MK-6169, A Potent Pan-genotype Hepatitis C Virus NS5A Inhibitor with Optimized Activity Against Common Resistance-Associated Substitutions. Journal of Medicinal Chemistry. PMID 29681153 DOI: 10.1021/Acs.Jmedchem.7B01927 |
0.052 |
|
1998 |
Ruck RT, Jones M. Bicyclo[2.2.1]heptan-1-ylcarbene can ring expand Tetrahedron Letters. 39: 4433-4436. DOI: 10.1016/S0040-4039(98)00840-5 |
0.04 |
|
2016 |
Tong L, Yu W, Coburn CA, Chen L, Selyutin O, Zeng Q, Dwyer MP, Nair AG, Shankar BB, Kim SH, Yang DY, Rosenblum SB, Ruck RT, Davies IW, Hu B, et al. Structure-activity relationships of proline modifications around the tetracyclic-indole class of NS5A inhibitors. Bioorganic & Medicinal Chemistry Letters. PMID 27680588 DOI: 10.1016/j.bmcl.2016.08.097 |
0.038 |
|
2016 |
Tong L, Yu W, Chen L, Selyutin O, Dwyer MP, Nair AG, Mazzola R, Kim JH, Sha D, Yin J, Ruck RT, Davies IW, Hu B, Zhong B, Hao J, et al. The Discovery of Ruzasvir (MK-8408): A Potent, Pan-genotype HCV NS5A Inhibitor with Optimized Activity Against Common Resistance-Associated Polymorphisms. Journal of Medicinal Chemistry. PMID 27808515 DOI: 10.1021/Acs.Jmedchem.6B01310 |
0.035 |
|
2012 |
He S, Ye Z, Truong Q, Shah S, Du W, Guo L, Dobbelaar PH, Lai Z, Liu J, Jian T, Qi H, Bakshi RK, Hong Q, Dellureficio J, Pasternak A, ... ... Ruck RT, et al. The Discovery of MK-4256, a Potent SSTR3 Antagonist as a Potential Treatment of Type 2 Diabetes. Acs Medicinal Chemistry Letters. 3: 484-9. PMID 24900499 DOI: 10.1021/ml300063m |
0.028 |
|
2012 |
Ruck RT, Huffman MA, Stewart GW, Cleator E, Kandur WV, Kim MM, Zhao D. Route development and multikilogram GMP delivery of a somatostatin receptor antagonist Organic Process Research and Development. 16: 1329-1337. DOI: 10.1021/op300128c |
0.015 |
|
Hide low-probability matches. |