| Year |
Citation |
Score |
| 2024 |
Schroeder EZ, Lin C, Hu Y, Dai ZY, Griffin AF, Hotvedt TS, Guzei IA, Schomaker JM. Chemoselective Silver-Catalyzed Nitrene Transfer: Tunable Syntheses of Azepines and Cyclic Carbamimidates. Journal of the American Chemical Society. PMID 39051463 DOI: 10.1021/jacs.4c08249 |
0.343 |
|
| 2024 |
Dequina HJ, Vine LE, Robey JT, Raskopf WT, Schomaker JM. Progress toward the Total Synthesis of Nogalamycin Using a Benzyne Cycloaddition Strategy. The Journal of Organic Chemistry. 89: 3491-3499. PMID 38372575 DOI: 10.1021/acs.joc.3c02921 |
0.311 |
|
| 2023 |
Dai ZY, Guzei IA, Schomaker JM. Iron-Catalyzed Site- and Regioselective 1,2-Azidoamidations of 1,3-Dienes. Organic Letters. 26: 269-273. PMID 38127720 DOI: 10.1021/acs.orglett.3c03947 |
0.359 |
|
| 2023 |
Trinh TA, Fu Y, Hu DB, Zappia SA, Guzei IA, Liu P, Schomaker JM. Chemo- and enantioselective intramolecular silver-catalyzed aziridinations of carbamimidates. Chemical Communications (Cambridge, England). PMID 38051226 DOI: 10.1039/d3cc05670h |
0.35 |
|
| 2023 |
Ward RM, Hu Y, Tu NP, Schomaker JM. Solvent effects on the chemo- and site-selectivity of transition metal-catalyzed nitrene transfer reactions: Alternatives to chlorinated solvents. Chemsuschem. e202300964. PMID 37696772 DOI: 10.1002/cssc.202300964 |
0.392 |
|
| 2022 |
Choi I, Trenerry MJ, Lee KS, King N, Berry JF, Schomaker JM. Divergent C-H Amidations and Imidations by Tuning Electrochemical Reaction Potentials. Chemsuschem. PMID 36166327 DOI: 10.1002/cssc.202201662 |
0.363 |
|
| 2022 |
Dequina HJ, Eshon J, Schmid SC, Raskopf WT, Sanders KM, Fernández I, Schomaker JM. Re-Evaluation of Product Outcomes in the Rh-Catalyzed Ring Expansion of Aziridines with -Sulfonyl-1,2,3-Triazoles. The Journal of Organic Chemistry. PMID 35947772 DOI: 10.1021/acs.joc.2c01186 |
0.354 |
|
| 2022 |
Nicastri KA, Zappia S, Pratt JC, Duncan JM, Guzei IA, Fernández I, Schomaker JM. Tunable Aziridinium Ylide Reactivity: Non-covalent Interactions Enable Divergent Product Outcomes. Acs Catalysis. 12: 1572-1580. PMID 35291380 DOI: 10.1021/acscatal.1c05413 |
0.351 |
|
| 2022 |
Fu Y, Zerull EE, Schomaker JM, Liu P. . Journal of the American Chemical Society. 144: 2735-2746. PMID 35130697 DOI: 10.1021/jacs.1c12111 |
0.358 |
|
| 2021 |
Ju M, Schomaker JM. Nitrene transfer catalysts for enantioselective C-N bond formation. Nature Reviews. Chemistry. 5: 580-594. PMID 37117585 DOI: 10.1038/s41570-021-00291-4 |
0.382 |
|
| 2021 |
Vine LE, Reeves RD, Landwehr EM, Fernández I, Schomaker JM. Scope and mechanistic investigations of Pd-catalyzed coupling/cyclizations and cycloisomerizations of allenyl malonates. Acs Catalysis. 11: 9485-9494. PMID 35832338 DOI: 10.1021/acscatal.1c01847 |
0.697 |
|
| 2021 |
Vine LE, Schomaker JM. Pd-catalyzed Heck-type Reactions of Allenes for Stereoselective Syntheses of Substituted 1,3-Dienes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34727393 DOI: 10.1002/chem.202103507 |
0.326 |
|
| 2021 |
Ward RM, Schomaker JM. Allene Trifunctionalization Amidyl Radical Cyclization and TEMPO Trapping. The Journal of Organic Chemistry. 86: 8891-8899. PMID 34125539 DOI: 10.1021/acs.joc.1c00675 |
0.314 |
|
| 2020 |
Reeves RD, Kinkema CN, Landwehr EM, Vine LE, Schomaker JM. Stereodivergent Metal-Catalyzed Allene Cycloisomerizations. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 11: 627-631. PMID 34219977 DOI: 10.1055/s-0037-1610746 |
0.701 |
|
| 2020 |
Carrasquel-Ursulaez W, Reeves RD, Dehghany M, Jones C, Schomaker JM, Chanda B. Re-evaluation of the mechanism of cytotoxicity of dialkylated lariat ether compounds. Rsc Advances. 10: 40391-40394. PMID 33732448 DOI: 10.1039/d0ra08494h |
0.629 |
|
| 2020 |
Dequina HJ, Schomaker JM. Aziridinium Ylides: Underutilized Intermediates for Complex Amine Synthesis. Trends in Chemistry. 2: 874-887. PMID 33665590 DOI: 10.1016/j.trechm.2020.08.003 |
0.303 |
|
| 2020 |
Ju M, Zerull E, Roberts JM, Huang M, Guzei IA, Schomaker JM. Silver-Catalyzed Enantioselective Propargylic C-H Bond Amination Through Rational Ligand Design. Journal of the American Chemical Society. PMID 32659081 DOI: 10.1021/Jacs.0C05726 |
0.476 |
|
| 2020 |
Liu L, Ward RM, Schomaker JM. Regioselective intramolecular allene amidation enabled by an EDA complex. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32449968 DOI: 10.1002/Chem.202002533 |
0.445 |
|
| 2020 |
Gerstner NC, Nicastri KA, Schomaker JM. Strategies for the Syntheses of Pactamycin and Jogyamycin. Angewandte Chemie (International Ed. in English). PMID 32392399 DOI: 10.1002/Anie.202004560 |
0.372 |
|
| 2020 |
Dequina HJ, Eshon J, Raskopf WT, Fernández I, Schomaker JM. Rh-Catalyzed Aziridine Ring Expansions to Dehydropiperazines. Organic Letters. PMID 32320259 DOI: 10.1021/Acs.Orglett.0C01124 |
0.413 |
|
| 2020 |
Eshon J, Nicastri KA, Schmid SC, Raskopf WT, Guzei IA, Fernández I, Schomaker JM. Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines through the intermediacy of aziridinium ylides. Nature Communications. 11: 1273. PMID 32152321 DOI: 10.1038/S41467-020-15134-X |
0.506 |
|
| 2020 |
Corbin J, Ketelboeter DR, Fernandez I, Schomaker JM. Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination. Journal of the American Chemical Society. PMID 32142272 DOI: 10.1021/Jacs.0C02441 |
0.48 |
|
| 2020 |
Vine LE, Zerull EE, Schomaker JM. Taming Nitrene Reactivity with Silver Catalysts Synlett. DOI: 10.1055/S-0040-1707197 |
0.399 |
|
| 2020 |
Reeves RD, Kinkema CN, Landwehr EM, Vine LE, Schomaker JM. Stereodivergent Metal-Catalyzed Allene Cycloisomerizations Synlett. 31: 627-631. DOI: 10.1055/S-0037-1610746 |
0.718 |
|
| 2020 |
Nicastri KA, Schomaker JM. 1,2-Azide Migration Enables Synthesis of β-Difluoroalkyl Azides Chem. 6: 327-329. DOI: 10.1016/J.Chempr.2020.01.016 |
0.396 |
|
| 2019 |
Liu L, Ward RM, Schomaker JM. Mechanistic Aspects and Synthetic Applications of Radical Additions to Allenes. Chemical Reviews. PMID 31833759 DOI: 10.1021/Acs.Chemrev.9B00312 |
0.42 |
|
| 2019 |
Ju M, Guan W, Schomaker JM, Harper KC. Sequential Reduction of Nitroalkanes Mediated by CS and Amidine/Guanidine Bases: A Controllable Nef Reaction. Organic Letters. PMID 31657582 DOI: 10.1021/Acs.Orglett.9B02987 |
0.456 |
|
| 2019 |
Gerstner NC, Schomaker JM. Stereocontrolled Synthesis of the Aminocyclopentitol Core of Jogyamycin via an Ichikawa Rearrangement Reaction. The Journal of Organic Chemistry. PMID 31578059 DOI: 10.1021/Acs.Joc.9B02249 |
0.454 |
|
| 2019 |
Scamp RJ, Scheffer B, Schomaker JM. Regioselective differentiation of vicinal methylene C-H bonds enabled by silver-catalysed nitrene transfer. Chemical Communications (Cambridge, England). PMID 31173000 DOI: 10.1039/C9Cc04006D |
0.834 |
|
| 2018 |
Eshon J, Gerstner NC, Schomaker JM. Oxidative allene amination for the synthesis of nitrogen-containing heterocycles. Arkivoc : Free Online Journal of Organic Chemistry. 2018: 204-233. PMID 31903453 DOI: 10.24820/Ark.5550190.P010.670 |
0.55 |
|
| 2018 |
Schmid SC, Guzei IA, Fernández I, Schomaker JM. Ring Expansion of Bicyclic Methyleneaziridines via Concerted, Near-Barrierless [2,3]-Stevens Rearrangements of Aziridinium Ylides. Acs Catalysis. 8: 7907-7914. PMID 30294503 DOI: 10.1021/Acscatal.8B02206 |
0.451 |
|
| 2018 |
Eshon J, Foarta F, Landis CR, Schomaker JM. α-Tetrasubstituted aldehydes through electronic and strain-controlled branch-selective stereoselective hydroformylation. The Journal of Organic Chemistry. PMID 30070109 DOI: 10.3389/Conf.Fchem.2018.01.00023 |
0.479 |
|
| 2018 |
Tansukawat ND, See AE, Jiranuntirat S, Corbin J, Schomaker JM. A Method for Small-Scale Production of Deuterochloroform. The Journal of Organic Chemistry. PMID 29864274 DOI: 10.1021/Acs.Joc.8B01018 |
0.389 |
|
| 2018 |
Alderson JM, Corbin JR, Schomaker JM. Investigation of transition metal-catalyzed nitrene transfer reactions in water. Bioorganic & Medicinal Chemistry. PMID 29681485 DOI: 10.1016/J.Bmc.2018.04.002 |
0.405 |
|
| 2018 |
Schomaker J, Mat Lani A. Site-Selective, Catalyst-Controlled Alkene Aziridination Synthesis. 50: 4462-4470. DOI: 10.1055/S-0037-1609858 |
0.436 |
|
| 2017 |
Huang M, Yang T, Paretsky J, Berry JF, Schomaker JM. Inverting Steric Effects: Using 'Attractive' Non-Covalent Interactions to Direct Silver-Catalyzed Nitrene Transfer. Journal of the American Chemical Society. PMID 29091737 DOI: 10.1021/Jacs.7B07619 |
0.508 |
|
| 2017 |
Schmid SC, Guzei IA, Schomaker JM. A Stereoselective [3+1] Ring Expansion for the Synthesis of Highly-Substituted Methylene Azetidines. Angewandte Chemie (International Ed. in English). PMID 28834110 DOI: 10.1002/Anie.201705202 |
0.468 |
|
| 2017 |
Burke EG, Schomaker JM. Synthetic Applications of Flexible SNO-OCT Strained Alkynes and their Use in Post-Polymerization Modifications. The Journal of Organic Chemistry. PMID 28795808 DOI: 10.1021/Acs.Joc.7B01506 |
0.331 |
|
| 2017 |
Alderson JM, Corbin JR, Schomaker JM. Tunable, Chemo- and Site-Selective Nitrene Transfer Reactions through the Rational Design of Silver(I) Catalysts. Accounts of Chemical Research. PMID 28787131 DOI: 10.1021/Acs.Accounts.7B00178 |
0.494 |
|
| 2017 |
Eshon J, Landis CR, Schomaker JM. Regioselective Rh-Catalyzed Hydroformylation of 1,1,3-Trisubstituted Allenes Using BisDiazaPhos Ligand. The Journal of Organic Chemistry. PMID 28621533 DOI: 10.1021/Acs.Joc.7B01140 |
0.441 |
|
| 2017 |
Ju M, Weatherly C, Guzei I, Schomaker JM. Chemo- and enantioselective intramolecular silver-catalyzed aziridination. Angewandte Chemie (International Ed. in English). PMID 28614622 DOI: 10.1002/Anie.201704786 |
0.818 |
|
| 2017 |
Reeves RD, Phelps AM, Raimbach WAT, Schomaker JM. Diastereoselective Au-Catalyzed Allene Cycloisomerizations to Highly Substituted Cyclopentenes. Organic Letters. PMID 28598168 DOI: 10.1021/Acs.Orglett.7B01350 |
0.76 |
|
| 2017 |
Liu L, Gerstner NC, Oxtoby LJ, Guzei IA, Schomaker JM. Fluorinated Amine Stereotriads via Allene Amination. Organic Letters. PMID 28573862 DOI: 10.1021/Acs.Orglett.7B01342 |
0.383 |
|
| 2017 |
Huang M, Corbin JR, Dolan NS, Fry CG, Vinokur AI, Guzei IA, Schomaker JM. Synthesis, Characterization, and Variable-Temperature NMR Studies of Silver(I) Complexes for Selective Nitrene Transfer. Inorganic Chemistry. PMID 28509541 DOI: 10.1021/Acs.Inorgchem.7B00838 |
0.398 |
|
| 2017 |
Burke EG, Gold B, Hoang TT, Raines RT, Schomaker JM. Fine-tuning Strain and Electronic Activation of Strain-promoted 1,3-Dipolar Cycloadditions with Endocyclic Sulfamates in SNO-OCTs. Journal of the American Chemical Society. PMID 28505435 DOI: 10.1021/Jacs.7B03943 |
0.334 |
|
| 2017 |
Schomaker JM, Alderson JM. Tandem Oxidative Derivatization of Nitrene Insertion Products for the Highly Diastereoselective Synthesis of 1,3-aminoalcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28486762 DOI: 10.1002/Chem.201702038 |
0.513 |
|
| 2017 |
Corbin JR, Schomaker JM. Tunable differentiation of tertiary C-H bonds in intramolecular transition metal-catalyzed nitrene transfer reactions. Chemical Communications (Cambridge, England). PMID 28367559 DOI: 10.1039/C7Cc01235G |
0.484 |
|
| 2017 |
Weatherly C, Alderson JM, Berry JF, Hein JE, Schomaker JM. Catalyst-Controlled Nitrene Transfer by Tuning Metal:Ligand Ratios: Insight into the Mechanisms of Chemoselectivity Organometallics. 36: 1649-1661. DOI: 10.1021/Acs.Organomet.7B00190 |
0.786 |
|
| 2016 |
Dolan N, Scamp RJ, Yang T, Berry JF, Schomaker JM. Catalyst-Controlled and Tunable, Chemoselective Silver-Catalyzed Intermolecular Nitrene Transfer: Experimental and Computational Studies. Journal of the American Chemical Society. PMID 27726353 DOI: 10.1021/Jacs.6B07981 |
0.808 |
|
| 2016 |
Gerstner NC, Adams CS, Tretbar M, Schomaker JM. Stereocontrolled Syntheses of Seven-Membered Carbocycles by Tandem Allene Aziridination/[4+3] Reaction. Angewandte Chemie (International Ed. in English). 55: 13240-13243. PMID 27709816 DOI: 10.1002/Anie.201606195 |
0.82 |
|
| 2016 |
Scamp RJ, Jirak JG, Dolan NS, Guzei IA, Schomaker JM. A General Catalyst for Site-Selective C(sp(3))-H Bond Amination of Activated Secondary over Tertiary Alkyl C(sp(3))-H Bonds. Organic Letters. PMID 27228003 DOI: 10.1021/Acs.Orglett.6B01392 |
0.808 |
|
| 2016 |
Phelps AM, Chan VS, Napolitano JG, Krabbe SW, Schomaker JM, Shekhar S. Ligand-Controlled Synthesis of Azoles via Ir-Catalyzed Reactions of Sulfoxonium Ylides with 2-Amino Heterocycles. The Journal of Organic Chemistry. PMID 27104299 DOI: 10.1021/Acs.Joc.6B00497 |
0.617 |
|
| 2016 |
Gerstner NC, Adams CS, Grigg RD, Tretbar M, Rigoli JW, Schomaker JM. Diastereoselective Synthesis of the Aminocyclitol Core of Jogyamycin via an Allene Aziridination Strategy. Organic Letters. PMID 26741730 DOI: 10.1021/Acs.Orglett.5B03453 |
0.772 |
|
| 2016 |
Touney EE, Van Hoveln R, Buttke CT, Freidberg MD, Guzei IA, Schomaker JM. Heteroleptic Nickel Complexes for the Markovnikov-Selective Hydroboration of Styrenes Organometallics. 35: 3436-3439. DOI: 10.1021/Acs.Organomet.6B00652 |
0.427 |
|
| 2015 |
Burke EG, Schomaker JM. Oxidative Allene Amination for the Synthesis of Azetidin-3-ones. Angewandte Chemie (International Ed. in English). 54: 12097-101. PMID 26387687 DOI: 10.1002/Anie.201504723 |
0.52 |
|
| 2015 |
Van Hoveln R, Hudson BM, Wedler HB, Bates DM, Le Gros G, Tantillo DJ, Schomaker JM. Mechanistic studies of copper(I)-catalyzed 1,3-halogen migration. Journal of the American Chemical Society. 137: 5346-54. PMID 25828031 DOI: 10.1021/Ja511236D |
0.454 |
|
| 2015 |
Schmid SC, Van Hoveln R, Rigoli JW, Schomaker JM. Development of N-Heterocyclic Carbene-Copper Complexes for 1,3-Halogen Migration Organometallics. 34: 4164-4173. DOI: 10.1021/Acs.Organomet.5B00629 |
0.807 |
|
| 2015 |
Croisant MF, Van Hoveln R, Schomaker JM. Formal Dyotropic Rearrangements in Organometallic Transformations European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201500561 |
0.421 |
|
| 2014 |
Van Hoveln RJ, Schmid SC, Tretbar M, Buttke CT, Schomaker JM. Formal Asymmetric Hydrobromination of Styrenes via Copper-Catalyzed 1,3-Halogen Migration. Chemical Science (Royal Society of Chemistry : 2010). 5: 4763-4767. PMID 26167268 DOI: 10.1039/C4Sc02040E |
0.824 |
|
| 2014 |
Alderson JM, Phelps AM, Scamp RJ, Dolan NS, Schomaker JM. Ligand-controlled, tunable silver-catalyzed C-H amination. Journal of the American Chemical Society. 136: 16720-3. PMID 25386769 DOI: 10.1021/Ja5094309 |
0.82 |
|
| 2014 |
Van Hoveln RJ, Schmid SC, Schomaker JM. 1,3-Halogen migration as an entry to aryl coppers from an unintuitive starting material. Organic & Biomolecular Chemistry. 12: 7655-8. PMID 25136932 DOI: 10.1039/C4Ob01294A |
0.418 |
|
| 2014 |
Adams CS, Weatherly CD, Burke EG, Schomaker JM. The conversion of allenes to strained three-membered heterocycles. Chemical Society Reviews. 43: 3136-63. PMID 24647416 DOI: 10.1039/C3Cs60416K |
0.804 |
|
| 2014 |
Rigoli JW, Guzei IA, Schomaker JM. Aminodiols via stereocontrolled oxidation of methyleneaziridines. Organic Letters. 16: 1696-9. PMID 24617556 DOI: 10.1021/Ol5003576 |
0.785 |
|
| 2014 |
Scamp RJ, Rigoli JW, Schomaker JM. Chemoselective silver-catalyzed nitrene insertion reactions Pure and Applied Chemistry. 86: 381-393. DOI: 10.1515/Pac-2014-5040 |
0.789 |
|
| 2014 |
Rigoli JW, Guzei IA, Schomaker JM. Ruthenium-Catalyzed Stereocontrolled Synthesis of Aminodiols Synfacts. 10: 608-608. DOI: 10.1055/S-0033-1339057 |
0.473 |
|
| 2014 |
Adams CS, Grigg RD, Schomaker JM. Complete stereodivergence in the synthesis of 2-amino-1,3-diols from allenes Chemical Science. 5: 3046-3056. DOI: 10.1039/C4Sc01214C |
0.814 |
|
| 2014 |
Adams CS, Grigg RD, Schomaker JM. Aminosugar motifs via an allene aziridination strategy Tetrahedron. 70: 4128-4134. DOI: 10.1016/J.Tet.2014.03.084 |
0.793 |
|
| 2013 |
Rigoli JW, Weatherly CD, Alderson JM, Vo BT, Schomaker JM. Tunable, chemoselective amination via silver catalysis. Journal of the American Chemical Society. 135: 17238-41. PMID 24187997 DOI: 10.1021/Ja406654Y |
0.814 |
|
| 2013 |
Rigoli JW, Weatherly CD, Vo BT, Neale S, Meis AR, Schomaker JM. Chemoselective allene aziridination via Ag(I) catalysis. Organic Letters. 15: 290-3. PMID 23265391 DOI: 10.1021/Ol303167N |
0.8 |
|
| 2013 |
Schomaker J, Grigg RD. Activating group recycling: A fresh approach to arene functionalization Synlett. 24: 401-407. DOI: 10.1055/S-0032-1317953 |
0.807 |
|
| 2013 |
Phelps AM, Dolan NS, Connell NT, Schomaker JM. Divergent reactivity of allene-containing α-diazoesters using Cu and Rh catalysis Tetrahedron. 69: 5614-5621. DOI: 10.1016/J.Tet.2013.03.014 |
0.459 |
|
| 2013 |
Weatherly CD, Guzei IA, Schomaker JM. Stereocontrolled synthesis of 1,3-diamino-2-ols by aminohydroxylation of bicyclic methylene-aziridines European Journal of Organic Chemistry. 3667-3670. DOI: 10.1002/Ejoc.201300416 |
0.796 |
|
| 2012 |
Grigg RD, Van Hoveln R, Schomaker JM. Copper-catalyzed recycling of halogen activating groups via 1,3-halogen migration. Journal of the American Chemical Society. 134: 16131-4. PMID 22985198 DOI: 10.1021/Ja306446M |
0.804 |
|
| 2012 |
Grigg RD, Rigoli JW, Van Hoveln R, Neale S, Schomaker JM. Beyond benzyl grignards: facile generation of benzyl carbanions from styrenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9391-6. PMID 22718528 DOI: 10.1002/Chem.201200642 |
0.816 |
|
| 2012 |
Adams CS, Boralsky LA, Guzei IA, Schomaker JM. Modular functionalization of allenes to aminated stereotriads. Journal of the American Chemical Society. 134: 10807-10. PMID 22708990 DOI: 10.1021/Ja304859W |
0.674 |
|
| 2012 |
Weatherly CD, Rigoli JW, Schomaker JM. Synthesis of 1,3-diaminated stereotriads via rearrangement of 1,4-diazaspiro[2.2]pentanes. Organic Letters. 14: 1704-7. PMID 22433023 DOI: 10.1021/Ol300269U |
0.819 |
|
| 2012 |
Rigoli JW, Boralsky LA, Hershberger JC, Marston D, Meis AR, Guzei IA, Schomaker JM. 1,4-Diazaspiro[2.2]pentanes as a flexible platform for the synthesis of diamine-bearing stereotriads. The Journal of Organic Chemistry. 77: 2446-55. PMID 22304460 DOI: 10.1021/Jo3000282 |
0.837 |
|
| 2012 |
Rigoli JW, Moyer SA, Pearce SD, Schomaker JM. α,β-Unsaturated imines via Ru-catalyzed coupling of allylic alcohols and amines. Organic & Biomolecular Chemistry. 10: 1746-9. PMID 22266838 DOI: 10.1039/C2Ob06921K |
0.786 |
|
| 2012 |
Grigg RD, Rigoli JW, Pearce SD, Schomaker JM. Synthesis of propargylic and allenic carbamates via the C-H amination of alkynes. Organic Letters. 14: 280-3. PMID 22182178 DOI: 10.1021/Ol203055V |
0.801 |
|
| 2012 |
Gladysz JA, Ball ZT, Bertrand G, Blum SA, Dong VM, Dorta R, Hahn FE, Humphrey MG, Jones WD, Klosin J, Manners I, Marks TJ, Mayer JM, Rieger B, Ritter JC, ... ... Schomaker JM, et al. Organometallics roundtable 2011 Organometallics. 31: 1-18. DOI: 10.1021/Om201234X |
0.722 |
|
| 2011 |
Kulshrestha A, Schomaker JM, Holmes D, Staples RJ, Jackson JE, Borhan B. Selectivity in the addition reactions of organometallic reagents to aziridine-2-carboxaldehydes: the effects of protecting groups and substitution patterns. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12326-39. PMID 21928447 DOI: 10.1002/Chem.201101168 |
0.74 |
|
| 2011 |
Boralsky LA, Marston D, Grigg RD, Hershberger JC, Schomaker JM. Allene functionalization via bicyclic methylene aziridines. Organic Letters. 13: 1924-7. PMID 21438516 DOI: 10.1021/Ol2002418 |
0.793 |
|
| 2011 |
Bergman R, Toste F, Boyd W, Crimmin M, Rosebrugh L, Schomaker J. Enantioselective Synthesis ofC2andC1Dienes Synfacts. 2011: 0183-0183. DOI: 10.1055/S-0030-1259337 |
0.771 |
|
| 2011 |
Guzei IA, Gunn EM, Spencer LC, Schomaker JM, Rigoli JW. Polymorphism of 5-(pyridin-2-ylmethylene)-3-phenyl-2-methylthio-3,5- dihydro-4H-imidazole-4-one Crystengcomm. 13: 3444-3450. DOI: 10.1039/C1Ce05098B |
0.736 |
|
| 2011 |
Grigg RD, Schomaker JM, Timokhin V. C-H amination/cyclocarbonylation of allene carbamates: A versatile platform for the synthesis of α,β-unsaturated γ-lactams Tetrahedron. 67: 4318-4326. DOI: 10.1016/J.Tet.2011.03.026 |
0.802 |
|
| 2010 |
Boyd WC, Crimmin MR, Rosebrugh LE, Schomaker JM, Bergman RG, Toste FD. Cobalt-mediated, enantioselective synthesis of C(2) and C(1) dienes. Journal of the American Chemical Society. 132: 16365-7. PMID 21033667 DOI: 10.1021/Ja107968C |
0.774 |
|
| 2009 |
Schomaker JM, Toste FD, Bergman RG. Cobalt-mediated [3 + 2]-annulation reaction of alkenes with alpha,beta-unsaturated ketones and imines. Organic Letters. 11: 3698-700. PMID 19639989 DOI: 10.1021/Ol901542N |
0.589 |
|
| 2008 |
Schomaker JM, Borhan B. Total synthesis of haterumalides NA and NC via a chromium-mediated macrocyclization. Journal of the American Chemical Society. 130: 12228-9. PMID 18722441 DOI: 10.1021/Ja8043695 |
0.624 |
|
| 2008 |
Schomaker JM, Boyd WC, Stewart IC, Toste FD, Bergman RG. Cobalt dinitrosoalkane complexes in the C-H functionalization of olefins. Journal of the American Chemical Society. 130: 3777-9. PMID 18318538 DOI: 10.1021/Ja800738D |
0.77 |
|
| 2007 |
Schomaker JM, Geiser AR, Huang R, Borhan B. Tetrasubstituted pyrrolidines via a tandem aza-Payne/hydroamination reaction. Journal of the American Chemical Society. 129: 3794-5. PMID 17348649 DOI: 10.1021/Ja068077W |
0.653 |
|
| 2007 |
Schomaker JM, Bhattacharjee S, Yan J, Borhan B. Diastereomerically and enantiomerically pure 2,3-disubstituted pyrrolidines from 2,3-aziridin-1-ols using a sulfoxonium ylide: a one-carbon homologative relay ring expansion. Journal of the American Chemical Society. 129: 1996-2003. PMID 17256932 DOI: 10.1021/Ja065833P |
0.667 |
|
| 2007 |
Schomaker JM, Bhattacharjee S, Yan J, Borhan B. Stereoselective Synthesis of Pyrrolidines from Aziridinols Synfacts. 2007: 582-582. DOI: 10.1055/S-2007-968582 |
0.648 |
|
| 2006 |
Delia TJ, Schomaker JM, Kalinda AS. The synthesis of substituted phenylpyrimidines via Suzuki coupling reactions Journal of Heterocyclic Chemistry. 43: 127-131. DOI: 10.1002/Jhet.5570430119 |
0.453 |
|
| 2005 |
Zheng T, Narayan RS, Schomaker JM, Borhan B. One-pot regio- and stereoselective cyclization of 1,2,n-triols. Journal of the American Chemical Society. 127: 6946-7. PMID 15884926 DOI: 10.1021/Ja043002I |
0.792 |
|
| 2004 |
Schomaker JM, Pulgam VR, Borhan B. Synthesis of diastereomerically and enantiomerically pure 2,3-disubstituted tetrahydrofurans using a sulfoxonium ylide. Journal of the American Chemical Society. 126: 13600-1. PMID 15493901 DOI: 10.1021/Ja0469075 |
0.654 |
|
| 2004 |
Schomaker JM, Borhan B. Total synthesis of (+)-tanikolide via oxidative lactonization. Organic & Biomolecular Chemistry. 2: 621-4. PMID 14770242 DOI: 10.1039/B311432E |
0.649 |
|
| 2004 |
Delia TJ, Anderson DP, Schomaker JM. 2,4,6-Trifluoropyrimidine. Reactions with nitrogen nucleophiles Journal of Heterocyclic Chemistry. 41: 991-993. DOI: 10.1002/Jhet.5570410623 |
0.433 |
|
| 2003 |
Schomaker JM, Travis BR, Borhan B. Direct lactonization of alkenols via osmium tetroxide-mediated oxidative cleavage. Organic Letters. 5: 3089-92. PMID 12916988 DOI: 10.1021/Ol035057F |
0.749 |
|
| 2001 |
Schomaker JM, Delia TJ. Arylation of halogenated pyrimidines via a Suzuki coupling reaction. The Journal of Organic Chemistry. 66: 7125-8. PMID 11597240 DOI: 10.1021/Jo010573+ |
0.43 |
|
| 2000 |
Schomaker JM, Delia TJ. 2,4,6-Trichloropyrimidine. Reaction with anilines Journal of Heterocyclic Chemistry. 37: 1457-1462. DOI: 10.1002/Jhet.5570370609 |
0.4 |
|
| 1999 |
Delia TJ, Meltsner BR, Schomaker JM. 2,4,6-Trichloropyrimidine. Reaction with sodium amide Journal of Heterocyclic Chemistry. 36: 1259-1261. DOI: 10.1002/Jhet.5570360524 |
0.432 |
|
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