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Justin T. Mohr, Ph.D. - Publications

Affiliations: 
2009 Chemistry California Institute of Technology, Pasadena, CA 
 2012- University of Illinois at Chicago, Chicago, IL, United States 
Website:
http://www2.chem.uic.edu/mohr/
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44 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Galaktionova DV, Siddiqui SY, Mohr JT. Remote Fluorination of α,β-Unsaturated Carbonyls via Silyl Dienol Ethers. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400493. PMID 38441174 DOI: 10.1002/chem.202400493  0.337
2023 Galaktionova D, Liu X, Chen X, Mohr JT. Iron-Catalyzed Gamma-Gamma Dimerization of Siloxydienes. Chemistry (Weinheim An Der Bergstrasse, Germany). e202302901. PMID 37903957 DOI: 10.1002/chem.202302901  0.528
2020 Grabovyi GA, Bhatti A, Mohr JT. Total Synthesis of Benzofuran-Based Aspergillusene B via Halogenative Aromatization of Enones. Organic Letters. 22: 4196-4200. PMID 32437168 DOI: 10.1021/Acs.Orglett.0C01259  0.792
2018 Defieber C, Mohr JT, Grabovyi GA, Stoltz BM. Short Enantioselective Formal Synthesis of (-)-Platencin. Synthesis. 50: 4359-4368. PMID 31061542 DOI: 10.1055/S-0037-1610437  0.815
2018 Mohr JT, Grabovyi GA. Synthetic studies toward the total synthesis of aeroplysinin Arkivoc. 2018: 215-230. DOI: 10.24820/Ark.5550190.P010.491  0.792
2017 Zhao M, Mohr JT. Vanadium(V)-mediated rearrangement/halogenation cascade: Synthesis of α-haloenones from propargyl alcohols Tetrahedron. 73: 4115-4124. DOI: 10.1016/J.Tet.2016.12.055  0.351
2017 Deng Y, Kauser NI, Islam SM, Mohr JT. AgII -Mediated Synthesis of β-Fluoroketones by Oxidative Cyclopropanol Opening European Journal of Organic Chemistry. 2017: 5872-5879. DOI: 10.1002/Ejoc.201700899  0.374
2016 Mohr JT, Moore JT, Stoltz BM. Enantioconvergent catalysis. Beilstein Journal of Organic Chemistry. 12: 2038-2045. PMID 27829909 DOI: 10.3762/bjoc.12.192  0.625
2016 Grabovyi GA, Mohr JT. Total Synthesis of Grifolin, Grifolic Acid, LL-Z1272α, LL-Z1272β, and Ilicicolinic Acid A. Organic Letters. PMID 27647101 DOI: 10.1021/Acs.Orglett.6B02469  0.804
2016 Liu X, Chen X, Mohr JT. Regiocontrolled Oxidative C-C Coupling of Dienol Ethers and 1,3-Dicarbonyl Compounds. Organic Letters. PMID 27280861 DOI: 10.1021/Acs.Orglett.6B01397  0.541
2016 Chen X, Liu X, Mohr JT. Cu-Catalyzed Stereoselective γ-Alkylation of Enones. Journal of the American Chemical Society. PMID 27159549 DOI: 10.1021/Jacs.6B02565  0.552
2016 Chen X, Liu X, Mohr JT. Direct Regioselective γ-Amination of Enones. Organic Letters. PMID 26840753 DOI: 10.1021/Acs.Orglett.5B03689  0.565
2016 Chen X, Liu X, Martinez JS, Mohr JT. Practical regioselective halogenation of vinylogous esters: Synthesis of differentiated mono-haloresorcinols and polyhalogenated resorcinols Tetrahedron. DOI: 10.1016/J.Tet.2016.02.006  0.595
2015 Liu X, Chen X, Mohr JT. Cascade Mn-mediated γ-Alkylation/oxa-Michael Addition of Enones with 1,3-Dicarbonyls. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26683524 DOI: 10.1002/Chem.201505027  0.571
2015 Craig RA, Loskot SA, Mohr JT, Behenna DC, Harned AM, Stoltz BM. Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones. Organic Letters. 17: 5160-3. PMID 26501770 DOI: 10.1021/Acs.Orglett.5B02376  0.807
2015 Liu X, Chen X, Mohr JT. Copper-Catalyzed γ-Sulfonylation of α,β-Unsaturated Carbonyl Compounds by Means of Silyl Dienol Ethers. Organic Letters. PMID 26132556 DOI: 10.1021/Acs.Orglett.5B01675  0.603
2015 Chen X, Martinez JS, Mohr JT. Regiodivergent halogenation of vinylogous esters: one-pot, transition-metal-free access to differentiated haloresorcinols. Organic Letters. 17: 378-81. PMID 25564873 DOI: 10.1021/Ol503561X  0.537
2014 Liu Y, Liniger M, McFadden RM, Roizen JL, Malette J, Reeves CM, Behenna DC, Seto M, Kim J, Mohr JT, Virgil SC, Stoltz BM. Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation. Beilstein Journal of Organic Chemistry. 10: 2501-12. PMID 25383121 DOI: 10.3762/Bjoc.10.261  0.811
2012 Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA. The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation. Journal of the American Chemical Society. 134: 19050-60. PMID 23102088 DOI: 10.1021/Ja306860N  0.765
2012 Zuhl AM, Mohr JT, Bachovchin DA, Niessen S, Hsu KL, Berlin JM, Dochnahl M, López-Alberca MP, Fu GC, Cravatt BF. Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition. Journal of the American Chemical Society. 134: 5068-71. PMID 22400490 DOI: 10.1021/Ja300799T  0.663
2011 Behenna DC, Mohr JT, Sherden NH, Marinescu SC, Harned AM, Tani K, Seto M, Ma S, Novák Z, Krout MR, McFadden RM, Roizen JL, Enquist JA, White DE, Levine SR, et al. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14199-223. PMID 22083969 DOI: 10.1002/Chem.201003383  0.699
2011 Bachovchin DA, Mohr JT, Speers AE, Wang C, Berlin JM, Spicer TP, Fernandez-Vega V, Chase P, Hodder PS, Schürer SC, Nomura DK, Rosen H, Fu GC, Cravatt BF. Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors. Proceedings of the National Academy of Sciences of the United States of America. 108: 6811-6. PMID 21398589 DOI: 10.1073/Pnas.1015248108  0.662
2011 Stoltz BM, Mohr JT. ChemInform Abstract: Protonation, Alkylation, Arylation, and Vinylation of Enolates Cheminform. 42: no-no. DOI: 10.1002/chin.201142247  0.529
2010 EWERS CLJ, HARRE M, MOHR J, NICKISCH K, TILSTAM U. ChemInform Abstract: An Efficient Synthesis of 17-epi-Ethynylestradiol. Cheminform. 29: no-no. DOI: 10.1002/chin.199832248  0.305
2009 Mohr JT, Krout MR, Stoltz BM. PREPARATION OF (S)-2-Allyl-2-methylcyclohexanone (Cyclohexanone, 2-methyl-2-(2-propen-1-yl)-, (2S)-). Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 86: 194-211. PMID 21197146 DOI: 10.15227/Orgsyn.086.0194  0.731
2009 Mohr JT, Hong AY, Stoltz BM. Enantioselective protonation. Nature Chemistry. 1: 359-69. PMID 20428461 DOI: 10.1038/nchem.297  0.47
2009 Krout MR, Mohr JT, Stoltz BM. PREPARATION OF (S)-tert-ButylPHOX (Oxazole, 4-(1,1-dimethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro- (4S)-). Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 86: 181. PMID 20072718 DOI: 10.15227/Orgsyn.086.0181  0.699
2009 Petrova KV, Mohr JT, Stoltz BM. Enantioselective total synthesis of (+)-cassiol. Organic Letters. 11: 293-5. PMID 19093836 DOI: 10.1021/Ol802410T  0.625
2009 Petrova KV, Mohr JT, Stoltz BM. Synthesis of (+)-Cassiol Synfacts. 2009: 712-712. DOI: 10.1055/S-0029-1217239  0.599
2009 Mohr JT, Krout MR, Stoltz BM. Preparation of (S)‐2‐Allyl‐2‐Methylcyclohexanone Organic Syntheses. 194-211. DOI: 10.1002/0471264229.Os086.20  0.561
2009 Krout MR, Mohr JT, Stoltz BM. Preparation of (S)-tert-ButylPHOX Organic Syntheses. 181-193. DOI: 10.1002/0471264229.Os086.19  0.527
2009 Kraut MR, Mohr JT, Stoltz BM, Schumacher A, Pfaltz A. Preparation of (s)-terf-butylPHOX (Oxazole,4-(1,1-dimethylethyl)-2-[2- (diphenyIphosphino)phenyl]-4,5-dihydro- (4S)-) Organic Syntheses. 86: 181-193.  0.421
2009 Mohr JT, Kraut MR, Stoltz BM, Ebner C, Pfaltz A. Preparation of (5)-2-Allyl-2-Methylcyclohexanone (Cyclohexanone, 2-Methyl-2-(2-Propen-1-Yl)-, (2S)-) Organic Syntheses. 86: 194-211.  0.462
2008 Mohr JT, Krout MR, Stoltz BM. Natural products as inspiration for the development of asymmetric catalysis. Nature. 455: 323-32. PMID 18800131 DOI: 10.1038/Nature07370  0.777
2008 Marinescu SC, Nishimata T, Mohr JT, Stoltz BM. Homogeneous pd-catalyzed enantioselective decarboxylative protonation. Organic Letters. 10: 1039-42. PMID 18303896 DOI: 10.1021/Ol702821J  0.649
2008 Marinescu SC, Nishimata T, Mohr JT, Stoltz BM. Synthesis of Chiral α-Substituted Ketones via Enantioselective Protonation Synfacts. 2008: 617-617. DOI: 10.1055/S-2008-1078398  0.61
2007 Mohr JT, Ebner DC, Stoltz BM. Catalytic enantioselective stereoablative reactions: an unexploited approach to enantioselective catalysis. Organic & Biomolecular Chemistry. 5: 3571-6. PMID 17971984 DOI: 10.1039/B711159M  0.788
2007 Mohr JT, Stoltz BM. Enantioselective Tsuji allylations. Chemistry, An Asian Journal. 2: 1476-91. PMID 17935094 DOI: 10.1002/Asia.200700183  0.65
2007 Keith JA, Behenna DC, Mohr JT, Ma S, Marinescu SC, Oxgaard J, Stoltz BM, Goddard WA. The inner-sphere process in the enantioselective Tsuji allylation reaction with (S)-t-Bu-phosphinooxazoline ligands. Journal of the American Chemical Society. 129: 11876-7. PMID 17824701 DOI: 10.1021/Ja070516J  0.8
2006 Mohr JT, Nishimata T, Behenna DC, Stoltz BM. Catalytic enantioselective decarboxylative protonation. Journal of the American Chemical Society. 128: 11348-9. PMID 16939246 DOI: 10.1021/Ja063335A  0.794
2006 Stoltz B, Mohr J, Nishimata T, Behenna D. Catalytic Enantioselective Decarboxylation-Protonation Synfacts. 2006: 1239-1239. DOI: 10.1055/S-2006-949497  0.767
2005 Mohr JT, Behenna DC, Harned AM, Stoltz BM. Deracemization of quaternary stereocenters by Pd-catalyzed enantioconvergent decarboxylative allylation of racemic beta-ketoesters. Angewandte Chemie (International Ed. in English). 44: 6924-7. PMID 16206310 DOI: 10.1002/Anie.200502018  0.798
2005 Mohr JT, Gribble GW, Lin SS, Eckenhoff RG, Cantor RS. Anesthetic potency of two novel synthetic polyhydric alkanols longer than the n-alkanol cutoff: evidence for a bilayer-mediated mechanism of anesthesia? Journal of Medicinal Chemistry. 48: 4172-6. PMID 15943489 DOI: 10.1021/Jm049459K  0.492
2005 Stoltz B, Mohr J, Behenna D, Harned A. Quaternary Carbon Center Formation by Decarboxylation of Allyl β-Ketoesters Synfacts. 2006: 0053-0053. DOI: 10.1055/S-2005-921674  0.761
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