| Year |
Citation |
Score |
| 2024 |
Rubel CZ, He WJ, Wisniewski SR, Engle KM. Benchtop Nickel Catalysis Invigorated by Electron-Deficient Diene Ligands. Accounts of Chemical Research. PMID 38236260 DOI: 10.1021/acs.accounts.3c00638 |
0.32 |
|
| 2024 |
Laudadio G, Neigenfind P, Péter Á, Rubel CZ, Emmanuel MA, Oderinde MS, El-Hayek Ewing T, Palkowitz MD, Sloane JL, Gillman KW, Ridge D, Mandler MD, Bolduc PN, Nicastri MC, Zhang B, ... ... Engle KM, et al. Nickel-Electrocatalytic Decarboxylative Arylation to Access Quaternary Centers. Angewandte Chemie (International Ed. in English). e202314617. PMID 38181042 DOI: 10.1002/anie.202314617 |
0.313 |
|
| 2023 |
Rubel CZ, Cao Y, El-Hayek Ewing T, Laudadio G, Beutner GL, Wisniewski SR, Wu X, Baran PS, Vantourout JC, Engle KM. Electroreductive Synthesis of Nickel(0) Complexes. Angewandte Chemie (International Ed. in English). e202311557. PMID 37984444 DOI: 10.1002/anie.202311557 |
0.308 |
|
| 2023 |
Hwang Y, Wisniewski SR, Engle KM. Ligand-Enabled Carboamidation of Unactivated Alkenes through Enhanced Organonickel Electrophilicity. Journal of the American Chemical Society. 145: 25293-25303. PMID 37938051 DOI: 10.1021/jacs.3c08855 |
0.367 |
|
| 2023 |
Ni HQ, Dai JC, Yang S, Loach RP, Chuba MD, McAlpine IJ, Engle KM. Catalytic σ-Bond Annulation with Ambiphilic Organohalides Enabled by β-X Elimination. Angewandte Chemie (International Ed. in English). e202306581. PMID 37306958 DOI: 10.1002/anie.202306581 |
0.343 |
|
| 2023 |
Ni HQ, Karunananda MK, Zeng T, Yang S, Liu Z, Houk KN, Liu P, Engle KM. Redox-Paired Alkene Difunctionalization Enables Skeletally Divergent Synthesis. Journal of the American Chemical Society. PMID 37220422 DOI: 10.1021/jacs.3c03274 |
0.808 |
|
| 2023 |
Simlandy AK, Alturaifi TM, Nguyen JM, Oxtoby LJ, Wong QN, Chen JS, Liu P, Engle KM. Enantioselective Hydroalkenylation and Hydroalkynylation of Alkenes Enabled by a Transient Directing Group: Catalyst Generality through Rigidification. Angewandte Chemie (International Ed. in English). e202304013. PMID 37141510 DOI: 10.1002/anie.202304013 |
0.829 |
|
| 2022 |
Gao Y, Kim N, Mendoza SD, Yazdani S, Faria-Vieira A, Liu M, Kendrick A, Grotjahn DB, Bertrand G, Jazzar R, Engle KM. (CAAC)Copper Catalysis Enables Regioselective Three-Component Carboboration of Terminal Alkynes. Acs Catalysis. 12: 7243-7247. PMID 37143933 DOI: 10.1021/acscatal.2c00614 |
0.389 |
|
| 2022 |
Tran VT, Kim N, Rubel CZ, Wu X, Kang T, Jankins TC, Li ZQ, Joannou MV, Ayers S, Gembicky M, Bailey J, Sturgell EJ, Sanchez BB, Chen JS, Lin S, ... ... Engle KM, et al. Structurally Diverse Bench-Stable Nickel(0) Pre-Catalysts: A Practical Toolkit for In Situ Ligation Protocols. Angewandte Chemie (International Ed. in English). PMID 36524997 DOI: 10.1002/anie.202211794 |
0.332 |
|
| 2022 |
Apolinar O, Kang T, Alturaifi TM, Bedekar PG, Rubel CZ, Derosa J, Sanchez BB, Wong QN, Sturgell EJ, Chen JS, Wisniewski SR, Liu P, Engle KM. Three-Component Asymmetric Ni-Catalyzed 1,2-Dicarbofunctionalization of Unactivated Alkenes via Stereoselective Migratory Insertion. Journal of the American Chemical Society. PMID 36222701 DOI: 10.1021/jacs.2c06636 |
0.731 |
|
| 2022 |
Liu Z, Oxtoby LJ, Sun J, Li ZQ, Kim N, Davies GHM, Engle KM. A Sterically Tuned Directing Auxiliary Promotes Catalytic 1,2-Carbofluorination of Alkenyl Carbonyl Compounds. Angewandte Chemie (International Ed. in English). PMID 36221812 DOI: 10.1002/anie.202214153 |
0.371 |
|
| 2022 |
Liu M, Sun J, Zhang T, Ding Y, Han YQ, Martín-Montero R, Lan Y, Shi BF, Engle KM. Regio- and Stereoselective 1,2-Oxyhalogenation of Non-Conjugated Alkynes via Directed Nucleopalladation: Catalytic Access to Tetrasubstituted Alkenes. Angewandte Chemie (International Ed. in English). e202209099. PMID 36082442 DOI: 10.1002/anie.202209099 |
0.583 |
|
| 2022 |
Li ZQ, He WJ, Ni HQ, Engle KM. Directed, nickel-catalyzed 1,2-alkylsulfenylation of alkenyl carbonyl compounds. Chemical Science. 13: 6567-6572. PMID 35756518 DOI: 10.1039/d2sc01563c |
0.352 |
|
| 2022 |
Jankins TC, Bell WC, Zhang Y, Qin ZY, Chen JS, Gembicky M, Liu P, Engle KM. Low-valent tungsten redox catalysis enables controlled isomerization and carbonylative functionalization of alkenes. Nature Chemistry. 14: 632-639. PMID 35655006 DOI: 10.1038/s41557-022-00951-y |
0.353 |
|
| 2022 |
Liu M, Sun J, Erbay T, Ni HQ, Martín-Montero R, Liu P, Engle KM. Pd(II)-Catalyzed C(alkenyl)-H Activation Facilitated by a Transient Directing Group. Angewandte Chemie (International Ed. in English). PMID 35467792 DOI: 10.1002/anie.202203624 |
0.447 |
|
| 2022 |
Li ZQ, Cao Y, Kang T, Engle KM. Electrophilic Sulfur Reagent Design Enables Directed -Carbosulfenylation of Unactivated Alkenes. Journal of the American Chemical Society. PMID 35436110 DOI: 10.1021/jacs.1c13252 |
0.393 |
|
| 2021 |
Liu B, Romine AM, Rubel CZ, Engle KM, Shi BF. Transition-Metal-Catalyzed, Coordination-Assisted Functionalization of Nonactivated C(sp)-H Bonds. Chemical Reviews. PMID 34714620 DOI: 10.1021/acs.chemrev.1c00519 |
0.52 |
|
| 2021 |
Li ZQ, Apolinar O, Deng R, Engle KM. Directed Markovnikov hydroarylation and hydroalkenylation of alkenes under nickel catalysis. Chemical Science. 12: 11038-11044. PMID 34522301 DOI: 10.1039/d1sc03121j |
0.424 |
|
| 2021 |
Jankins TC, Martin-Montero R, Cooper P, Martin R, Engle KM. Low-Valent Tungsten Catalysis Enables Site-Selective Isomerization-Hydroboration of Unactivated Alkenes. Journal of the American Chemical Society. 143: 14981-14986. PMID 34498848 DOI: 10.1021/jacs.1c07162 |
0.354 |
|
| 2021 |
Romine AM, Demer MJ, Gembicky M, Rheingold AL, Engle KM. Ligand Rearrangement Leads to Tetrahydrothiophene-Functionalized -Heterocyclic Carbene Palladium(II) Complexes. Organometallics. 40: 2311-2319. PMID 34433997 DOI: 10.1021/acs.organomet.1c00041 |
0.325 |
|
| 2021 |
Matsuura R, Karunananda MK, Liu M, Nguyen N, Blackmond DG, Engle KM. Mechanistic Studies of Pd(II)-Catalyzed / Isomerization of Unactivated Alkenes: Evidence for a Monometallic Nucleopalladation Pathway. Acs Catalysis. 11: 4239-4246. PMID 34422450 DOI: 10.1021/acscatal.1c00783 |
0.785 |
|
| 2021 |
Ni HQ, Li ZQ, Tran VT, Engle KM. Modular synthesis of non-conjugated -(quinolin-8-yl) alkenyl amides via cross-metathesis. Tetrahedron. 93. PMID 34393281 DOI: 10.1016/j.tet.2021.132279 |
0.366 |
|
| 2021 |
Kleinmans R, Apolinar O, Derosa J, Karunananda MK, Li ZQ, Tran VT, Wisniewski SR, Engle KM. Ni-Catalyzed 1,2-Diarylation of Alkenyl Ketones: A Comparative Study of Carbonyl-Directed Reaction Systems. Organic Letters. PMID 34213351 DOI: 10.1021/acs.orglett.1c01447 |
0.837 |
|
| 2021 |
Gao Y, Yazdani S, Kendrick A, Junor GP, Kang T, Grotjahn DB, Bertrand G, Jazzar R, Engle KM. Cyclic(Alkyl)(Amino)Carbene Ligands Enable Cu-Catalyzed Markovnikov Protoboration and Protosilylation of Terminal Alkynes: A Versatile Portal to Functionalized Alkenes. Angewandte Chemie (International Ed. in English). PMID 34159696 DOI: 10.1002/anie.202106107 |
0.423 |
|
| 2021 |
Liu Z, Oxtoby LJ, Liu M, Li ZQ, Tran VT, Gao Y, Engle KM. A Transient Directing Group Strategy Enables Enantioselective Multicomponent Organofluorine Synthesis. Journal of the American Chemical Society. PMID 34077182 DOI: 10.1021/jacs.1c03178 |
0.335 |
|
| 2021 |
Liu M, Tang T, Apolinar O, Matsuura R, Busacca CA, Qu B, Fandrick DR, Zatolochnaya OV, Senanayake CH, Song JJ, Engle KM. Atom-Economical Cross-Coupling of Internal and Terminal Alkynes to Access 1,3-Enynes. Journal of the American Chemical Society. PMID 33683868 DOI: 10.1021/jacs.0c12565 |
0.458 |
|
| 2020 |
Wang X, Li ZQ, Mai BK, Gurak JA, Xu JE, Tran VT, Ni HQ, Liu Z, Liu Z, Yang KS, Xiang R, Liu P, Engle KM. Controlling cyclization pathways in palladium(ii)-catalyzed intramolecular alkene hydro-functionalization substrate directivity. Chemical Science. 11: 11307-11314. PMID 35382446 DOI: 10.1039/d0sc03409f |
0.83 |
|
| 2020 |
Derosa J, Apolinar O, Kang T, Tran VT, Engle KM. Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes. Chemical Science. 11: 4287-4296. PMID 34122886 DOI: 10.1039/c9sc06006e |
0.677 |
|
| 2020 |
Kang T, Erbay TG, Xu KL, Gallego GM, Burtea A, Nair SK, Patman RL, Zhou R, Sutton SC, McAlpine IJ, Liu P, Engle KM. Multifaceted Substrate-Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds. Acs Catalysis. 10: 13075-13083. PMID 33791144 DOI: 10.1021/acscatal.0c03622 |
0.388 |
|
| 2020 |
Liu Z, Gao Y, Zeng T, Engle KM. Transition-Metal-Catalyzed 1,2-Carboboration of Alkenes: Strategies, Mechanisms, and Stereocontrol. Israel Journal of Chemistry. 60: 219-229. PMID 33785969 DOI: 10.1002/ijch.201900087 |
0.414 |
|
| 2020 |
Ni HQ, Kevlishvili I, Bedekar PG, Barber JS, Yang S, Tran-Dubé M, Romine AM, Lu HX, McAlpine IJ, Liu P, Engle KM. Anti-selective [3+2] (Hetero)annulation of non-conjugated alkenes via directed nucleopalladation. Nature Communications. 11: 6432. PMID 33353940 DOI: 10.1038/s41467-020-20182-4 |
0.39 |
|
| 2020 |
Li ZQ, Fu Y, Deng R, Tran VT, Gao Y, Liu P, Engle KM. Ligand-Controlled Regiodivergence in Nickel-Catalyzed Hydroarylation and Hydroalkenylation of Alkenyl Carboxylic Acids. Angewandte Chemie (International Ed. in English). PMID 32894810 DOI: 10.1002/Anie.202010840 |
0.395 |
|
| 2020 |
Gao Y, Wu ZQ, Engle KM. Synthesis of Stereodefined 1,1-Diborylalkenes via Copper-Catalyzed Diboration of Terminal Alkynes. Organic Letters. PMID 32574499 DOI: 10.1021/Acs.Orglett.0C01901 |
0.494 |
|
| 2020 |
Gao DW, Gao Y, Shao H, Qiao TZ, Wang X, Sanchez BB, Chen JS, Liu P, Engle KM. Cascade CuH-Catalysed Conversion of Alkynes to Enantioenriched 1,1-Disubstituted Products. Nature Catalysis. 3: 23-29. PMID 32420528 DOI: 10.1038/s41929-019-0384-6 |
0.777 |
|
| 2020 |
Vasquez AM, Gurak JA, Joe C, Cherney EC, Engle KM. Catalytic α-Hydroarylation of Acrylates and Acrylamides via an Interrupted Hydrodehalogenation Reaction. Journal of the American Chemical Society. PMID 32379433 DOI: 10.1021/Jacs.0C03040 |
0.434 |
|
| 2020 |
Oxtoby L, Li ZQ, Tran V, Erbay T, Deng R, Liu P, Engle KM. A Transient Directing Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes. Angewandte Chemie (International Ed. in English). PMID 32196876 DOI: 10.1002/Anie.202001069 |
0.501 |
|
| 2020 |
Tran V, Li ZQ, Apolinar O, Derosa J, Wisniewski S, Joannou MV, Eastgate M, Engle KM. Ni(COD)(DQ): An Air-Stable 18-Electron Ni(0)-Olefin Precatalyst. Angewandte Chemie (International Ed. in English). PMID 32065839 DOI: 10.1002/Anie.202000124 |
0.658 |
|
| 2020 |
Tran V, Li ZQ, Gallagher T, Derosa J, Liu P, Engle KM. Integrating Allyl Electrophiles into Nickel-Catalyzed Conjunctive Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 31958202 DOI: 10.1002/Anie.201915454 |
0.739 |
|
| 2020 |
Tran VT, Nimmagadda SK, Liu M, Engle KM. Recent applications of chiral phosphoric acids in palladium catalysis. Organic & Biomolecular Chemistry. PMID 31907504 DOI: 10.1039/C9Ob02205H |
0.835 |
|
| 2020 |
Derosa J, Apolinar O, Kang T, Tran VT, Engle KM. Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes Chemical Science. 11: 4287-4296. DOI: 10.1039/C9Sc06006E |
0.674 |
|
| 2019 |
Medina JM, Kang T, Erbay TG, Shao H, Gallego GM, Yang S, Tran-Dubé M, Richardson PF, Derosa J, Helsel RT, Patman RL, Wang F, Ashcroft CP, Braganza JF, McAlpine I, ... ... Engle KM, et al. Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization, (Hetero)Aryl Scope, and Origins of Pathway Selectivity. Acs Catalysis. 9: 11130-11136. PMID 32617185 DOI: 10.1021/Acscatal.9B03557 |
0.798 |
|
| 2019 |
Oxtoby LJ, Gurak JA, Wisniewski SR, Eastgate MD, Engle KM. Palladium-Catalyzed Reductive Heck Coupling of Alkenes. Trends in Chemistry. 1: 572-587. PMID 32542234 DOI: 10.1016/j.trechm.2019.05.007 |
0.385 |
|
| 2019 |
Romine AM, Yang KS, Karunananda MK, Chen JS, Engle KM. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis. Acs Catalysis. 9: 7626-7640. PMID 32542117 DOI: 10.1021/Acscatal.9B01471 |
0.837 |
|
| 2019 |
Liu Z, Li X, Zeng T, Engle KM. Directed, Palladium(II)-Catalyzed Enantioselective anti-Carboboration of Alkenyl Carbonyl Compounds. Acs Catalysis. 9: 3260-3265. PMID 31799023 DOI: 10.1021/Acscatal.9B00181 |
0.626 |
|
| 2019 |
Jankins TC, Qin Z, Engle KM. A practical method for N-alkylation of phosphinic (thio)amides with alcohols via transfer hydrogenation. Tetrahedron. 75: 3272-3281. PMID 31745374 DOI: 10.1016/J.Tet.2019.04.029 |
0.352 |
|
| 2019 |
Derosa J, Kang T, Tran VT, Wisniewski S, Karunananda MK, Jankins TC, Xu KL, Engle KM. Nickel-Catalyzed 1,2-Diarylation of Alkenyl Carboxylates: A Gateway to 1,2,3-Trifunctionalized Building Blocks. Angewandte Chemie (International Ed. in English). PMID 31693286 DOI: 10.1002/Anie.201913062 |
0.833 |
|
| 2019 |
Lv H, Kang H, Zhou B, Xue X, Engle KM, Zhao D. Nickel-catalyzed intermolecular oxidative Heck arylation driven by transfer hydrogenation. Nature Communications. 10: 5025. PMID 31690717 DOI: 10.1038/S41467-019-12949-1 |
0.504 |
|
| 2019 |
Liu Z, Chen J, Lu HX, Li X, Gao Y, Coombs J, Goldfogel M, Engle KM. Pd(0)-Catalyzed Directed syn-1,2-Carboboration and -Silylation: Alkene Scope, Applications in Dearomatization, and Stereocontrol via a Chiral Auxiliary. Angewandte Chemie (International Ed. in English). PMID 31538388 DOI: 10.1002/Anie.201910304 |
0.591 |
|
| 2019 |
Nimmagadda SK, Liu M, Karunananda MK, Gao DW, Apolinar O, Chen JS, Liu P, Engle KM. Catalytic, Enantioselective α-Alkylation of Azlactones with Non-Conjugated Alkenes via Directed Nucleopalladation. Angewandte Chemie (International Ed. in English). PMID 30729619 DOI: 10.1002/Anie.201814272 |
0.8 |
|
| 2019 |
Medina JM, Kang T, Erbay TG, Shao H, Gallego GM, Yang S, Tran-Dubé M, Richardson PF, Derosa J, Helsel RT, Patman RL, Wang F, Ashcroft CP, Braganza JF, McAlpine I, ... ... Engle KM, et al. Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization, (Hetero)Aryl Scope, and Origins of Pathway Selectivity Acs Catalysis. 9: 11130-11136. DOI: 10.1021/acscatal.9b03557 |
0.751 |
|
| 2019 |
Romine AM, Yang KS, Karunananda MK, Chen JS, Engle KM. Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis Acs Catalysis. 9: 7626-7640. DOI: 10.1021/ACSCATAL.9B01471 |
0.796 |
|
| 2019 |
Liu Z, Gao Y, Zeng T, Engle KM. Transition‐Metal‐Catalyzed 1,2‐Carboboration of Alkenes: Strategies, Mechanisms, and Stereocontrol Israel Journal of Chemistry. 60: 219-229. DOI: 10.1002/Ijch.201900087 |
0.523 |
|
| 2018 |
Luo SX, Engle KM, Dong X, Hejl A, Takase MK, Henling LM, Liu P, Houk KN, Grubbs RH. An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes. Acs Catalysis. 8: 4600-4611. PMID 32528741 DOI: 10.1021/Acscatal.8B00843 |
0.768 |
|
| 2018 |
O'Duill ML, Engle KM. Protodepalladation as a Strategic Elementary Step in Catalysis. Synthesis. 50: 4699-4714. PMID 31105348 DOI: 10.1055/S-0037-1611064 |
0.825 |
|
| 2018 |
Gao DW, Xiao Y, Liu M, Liu Z, Karunananda MK, Chen JS, Engle KM. Catalytic, Enantioselective Synthesis of Allenyl Boronates. Acs Catalysis. 8: 3650-3654. PMID 30740261 DOI: 10.1021/Acscatal.8B00626 |
0.838 |
|
| 2018 |
Matsuura R, Jankins TC, Hill DE, Yang KS, Gallego GM, Yang S, He M, Wang F, Marsters RP, McAlpine I, Engle KM. Palladium(ii)-catalyzed γ-selective hydroarylation of alkenyl carbonyl compounds with arylboronic acids. Chemical Science. 9: 8363-8368. PMID 30542583 DOI: 10.1039/C8Sc03081B |
0.825 |
|
| 2018 |
Derosa J, Kleinmans R, Tran VT, Karunananda MK, Wisniewski SR, Eastgate MD, Engle KM. Nickel-Catalyzed 1,2-Diarylation of Simple Alkenyl Amides. Journal of the American Chemical Society. PMID 30525575 DOI: 10.1021/Jacs.8B11942 |
0.838 |
|
| 2018 |
Gurak JA, Engle KM. Practical Intermolecular Hydroarylation of Terminal Alkenes via Reductive Heck Coupling. Acs Catalysis. 8: 8987-8992. PMID 30393575 DOI: 10.1021/Acscatal.8B02717 |
0.515 |
|
| 2018 |
Tran VT, Gurak JA, Yang KS, Engle KM. Activation of diverse carbon-heteroatom and carbon-carbon bonds via palladium(II)-catalysed β-X elimination. Nature Chemistry. PMID 30127512 DOI: 10.1038/S41557-018-0110-Z |
0.824 |
|
| 2018 |
Derosa J, van der Puyl VA, Tran VT, Liu M, Engle KM. Directed nickel-catalyzed 1,2-dialkylation of alkenyl carbonyl compounds. Chemical Science. 9: 5278-5283. PMID 29997883 DOI: 10.1039/C8Sc01735B |
0.715 |
|
| 2018 |
Gao DW, Vinogradova EV, Nimmagadda SK, Medina JM, Xiao Y, Suciu RM, Cravatt BF, Engle KM. Direct Access to Versatile Electrophiles via Catalytic Oxidative Cyanation of Alkenes. Journal of the American Chemical Society. PMID 29894184 DOI: 10.1021/Jacs.8B03704 |
0.814 |
|
| 2018 |
Zeng T, Liu Z, Schmidt MA, Eastgate MD, Engle KM. Directed, Palladium(II)-Catalyzed Intermolecular Aminohydroxylation of Alkenes Using a Mild Oxidation System. Organic Letters. PMID 29888604 DOI: 10.1021/Acs.Orglett.8B01440 |
0.574 |
|
| 2018 |
Liu M, Yang P, Karunananda MK, Wang Y, Liu P, Engle KM. C(alkenyl)-H Activation via Six-Membered Palladacycles: Catalytic 1,3-Diene Synthesis. Journal of the American Chemical Society. PMID 29630359 DOI: 10.1021/Jacs.8B02124 |
0.818 |
|
| 2018 |
Derosa J, O'Duill ML, Holcomb M, Boulous MN, Patman RL, Wang F, Tran-Dubé M, McAlpine I, Engle KM. Copper-Catalyzed Chan-Lam Cyclopropylation of Phenols and Azaheterocycles. The Journal of Organic Chemistry. PMID 29498847 DOI: 10.1021/Acs.Joc.7B03100 |
0.813 |
|
| 2018 |
Liu Z, Ni HQ, Zeng T, Engle KM. Catalytic Carbo- and Aminoboration of Alkenyl Carbonyl Compounds via 5- and 6-Membered Palladacycles. Journal of the American Chemical Society. PMID 29384373 DOI: 10.1021/Jacs.8B00881 |
0.576 |
|
| 2018 |
van der Puyl VA, Derosa J, Engle KM. Directed, Nickel-Catalyzed Umpolung 1,2-Carboamination of Alkenyl Carbonyl Compounds Acs Catalysis. 9: 224-229. DOI: 10.1021/Acscatal.8B04516 |
0.728 |
|
| 2018 |
Luo S, Engle KM, Dong X, Hejl A, Takase MK, Henling LM, Liu P, Houk KN, Grubbs RH. An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes Acs Catalysis. 8: 4600-4611. DOI: 10.1021/acscatal.8b00843 |
0.787 |
|
| 2017 |
O'Duill ML, Matsuura R, Wang Y, Turnbull JL, Gurak JA, Gao DW, Lu G, Liu P, Engle KM. Tridentate Directing Groups Stabilize 6-Membered Palladacycles in Catalytic Alkene Hydrofunctionalization. Journal of the American Chemical Society. PMID 28972751 DOI: 10.1021/Jacs.7B08383 |
0.811 |
|
| 2017 |
Derosa J, Tran V, Boulous MN, Chen JS, Engle KM. Nickel-Catalyzed β,γ-Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Conjunctive Cross-Coupling. Journal of the American Chemical Society. PMID 28738150 DOI: 10.1021/Jacs.7B06567 |
0.722 |
|
| 2017 |
Liu Z, Wang Y, Wang Z, Zeng T, Liu P, Engle KM. Catalytic Intermolecular Carboamination of Unactivated Alkenes via Directed Aminopalladation. Journal of the American Chemical Society. PMID 28727452 DOI: 10.1021/Jacs.7B06520 |
0.61 |
|
| 2017 |
Derosa J, Cantu AL, Boulous MN, O'Duill ML, Turnbull JL, Liu Z, De La Torre DM, Engle KM. Palladium(II)-Catalyzed Directed anti-Hydrochlorination of Unactivated Alkynes with HCl. Journal of the American Chemical Society. PMID 28266849 DOI: 10.1021/Jacs.7B00892 |
0.832 |
|
| 2017 |
Engle K, Gurak J. Regioselective Hydroamination Using a Directed Nucleopalladation/Protodepalladation Strategy Synlett. 28: 2057-2065. DOI: 10.1055/S-0036-1589077 |
0.485 |
|
| 2017 |
Gurak JA, Tran VT, Sroda MM, Engle KM. N-alkylation of 2-pyridone derivatives via palladium(II)-catalyzed directed alkene hydroamination Tetrahedron. 73: 3636-3642. DOI: 10.1016/J.Tet.2017.03.091 |
0.543 |
|
| 2016 |
Liu Z, Zeng T, Yang KS, Engle KM. β,γ-Vicinal Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Directed Nucleopalladation. Journal of the American Chemical Society. PMID 27779861 DOI: 10.1021/Jacs.6B09170 |
0.832 |
|
| 2016 |
Yang KS, Gurak JA, Liu Z, Engle KM. Catalytic, Regioselective Hydrocarbofunctionalization of Unactivated Alkenes with Diverse C-H Nucleophiles. Journal of the American Chemical Society. PMID 27709911 DOI: 10.1021/Jacs.6B08850 |
0.841 |
|
| 2016 |
Luo SX, Cannon JS, Taylor BL, Engle KM, Houk KN, Grubbs RH. Z-Selective Cross-Metathesis and Homodimerization of 3E-1,3-Dienes: Reaction Optimization, Computational Analysis, and Synthetic Applications. Journal of the American Chemical Society. PMID 27689541 DOI: 10.1021/Jacs.6B08387 |
0.826 |
|
| 2016 |
Pfeifer L, Engle KM, Pidgeon GW, Sparkes HA, Thompson AL, Brown JM, Gouverneur VE. Hydrogen-Bonded Homoleptic Fluoride-Diarylurea Complexes: Structure, Reactivity and Coordinating Power. Journal of the American Chemical Society. PMID 27608274 DOI: 10.1021/Jacs.6B07501 |
0.72 |
|
| 2016 |
Liu Z, Derosa J, Engle KM. Palladium(II)-Catalyzed Regioselective syn-Hydroarylation of Disubstituted Alkynes Using a Removable Directing Group. Journal of the American Chemical Society. PMID 27602748 DOI: 10.1021/Jacs.6B08818 |
0.765 |
|
| 2016 |
Lee J, Grandner JM, Engle KM, Houk KN, Grubbs RH. In Situ Catalyst Modification in Atom Transfer Radical Reactions with Ruthenium Benzylidene Complexes. Journal of the American Chemical Society. 138: 7171-7. PMID 27186790 DOI: 10.1021/Jacs.6B03767 |
0.62 |
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| 2016 |
Yang KS, Engle KM. Organic chemistry: Precision pruning of molecules. Nature. 533: 183-184. PMID 27172040 DOI: 10.1038/533183A |
0.824 |
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| 2016 |
Gurak JA, Yang KS, Liu Z, Engle KM. Directed, Regiocontrolled Hydroamination of Unactivated Alkenes via Protodepalladation. Journal of the American Chemical Society. PMID 27093112 DOI: 10.1021/Jacs.6B02718 |
0.843 |
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| 2016 |
Engle KM. The mechanism of palladium(II)-mediated C-H cleavage with mono-N-protected amino acid (MPAA) ligands: Origins of rate acceleration Pure and Applied Chemistry. 88: 119-138. DOI: 10.1515/Pac-2015-0902 |
0.386 |
|
| 2015 |
Engle KM, Pfeifer L, Pidgeon GW, Giuffredi GT, Thompson AL, Paton RS, Brown JM, Gouverneur V. Coordination diversity in hydrogen-bonded homoleptic fluoride-alcohol complexes modulates reactivity. Chemical Science. 6: 5293-5302. PMID 29449931 DOI: 10.1039/C5Sc01812A |
0.682 |
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| 2015 |
Engle KM, Dastbaravardeh N, Thuy-Boun PS, Wang DH, Sather AC, Yu JQ. Ligand-Accelerated ortho-C-H Olefination of Phenylacetic Acids. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 92: 58-75. PMID 27397943 DOI: 10.15227/Orgsyn.092.0058 |
0.645 |
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| 2015 |
Engle KM, Lu G, Luo SX, Henling LM, Takase MK, Liu P, Houk KN, Grubbs RH. Origins of initiation rate differences in ruthenium olefin metathesis catalysts containing chelating benzylidenes. Journal of the American Chemical Society. 137: 5782-92. PMID 25897653 DOI: 10.1021/Jacs.5B01144 |
0.797 |
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| 2015 |
Koy M, Engle KM, Henling LM, Takase MK, Grubbs RH. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic Letters. 17: 1986-9. PMID 25853213 DOI: 10.1021/Acs.Orglett.5B00743 |
0.578 |
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| 2015 |
Engle KM, Luo SX, Grubbs RH. An S(N)Ar approach to sterically hindered ortho-alkoxybenzaldehydes for the synthesis of olefin metathesis catalysts. The Journal of Organic Chemistry. 80: 4213-20. PMID 25826714 DOI: 10.1021/Acs.Joc.5B00563 |
0.821 |
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| 2015 |
Wang XC, Gong W, Fang LZ, Zhu RY, Li S, Engle KM, Yu JQ. Ligand-enabled meta-C-H activation using a transient mediator. Nature. 519: 334-8. PMID 25754328 DOI: 10.1038/nature14214 |
0.704 |
|
| 2015 |
Engle KM, Pfeifer L, Pidgeon GW, Giuffredi GT, Thompson AL, Paton RS, Brown JM, Gouverneur V. Coordination diversity in hydrogen-bonded homoleptic fluoride-alcohol complexes modulates reactivity Chemical Science. 6: 5293-5302. DOI: 10.1039/c5sc01812a |
0.608 |
|
| 2015 |
Engle KM, Luo S, Grubbs RH. ChemInform Abstract: An SNAr Approach to Sterically Hindered ortho-Alkoxybenzaldehydes for the Synthesis of Olefin Metathesis Catalysts. Cheminform. 46: no-no. DOI: 10.1002/chin.201535086 |
0.781 |
|
| 2015 |
Koy M, Engle KM, Henling LM, Takase MK, Grubbs RH. ChemInform Abstract: Synthesis of Substituted Dihydrobenzofurans via Tandem SNAr/5-exo-trig Cyclization. Cheminform. 46: no-no. DOI: 10.1002/chin.201530147 |
0.46 |
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| 2013 |
Wolstenhulme JR, Rosenqvist J, Lozano O, Ilupeju J, Wurz N, Engle KM, Pidgeon GW, Moore PR, Sandford G, Gouverneur V. Asymmetric electrophilic fluorocyclization with carbon nucleophiles. Angewandte Chemie (International Ed. in English). 52: 9796-800. PMID 23873744 DOI: 10.1002/Anie.201304845 |
0.651 |
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| 2013 |
Wang H, Li G, Engle KM, Yu JQ, Davies HM. Sequential C-H functionalization reactions for the enantioselective synthesis of highly functionalized 2,3-dihydrobenzofurans. Journal of the American Chemical Society. 135: 6774-7. PMID 23600441 DOI: 10.1021/Ja401731D |
0.637 |
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| 2013 |
Engle KM, Yu JQ. Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate. The Journal of Organic Chemistry. 78: 8927-55. PMID 23565982 DOI: 10.1021/Jo400159Y |
0.622 |
|
| 2013 |
Mizuta S, Engle KM, Verhoog S, Galicia-López O, O'Duill M, Médebielle M, Wheelhouse K, Rassias G, Thompson AL, Gouverneur V. Trifluoromethylation of allylsilanes under photoredox catalysis. Organic Letters. 15: 1250-3. PMID 23465076 DOI: 10.1021/Ol400184T |
0.806 |
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| 2013 |
Mizuta S, Verhoog S, Engle KM, Khotavivattana T, O'Duill M, Wheelhouse K, Rassias G, Médebielle M, Gouverneur V. Catalytic hydrotrifluoromethylation of unactivated alkenes. Journal of the American Chemical Society. 135: 2505-8. PMID 23373772 DOI: 10.1021/Ja401022X |
0.776 |
|
| 2013 |
Engle KM, Yu J. ChemInform Abstract: Transition Metal Catalyzed C-H Functionalization. Synthetically Enabling Reactions for Building Molecular Complexity Cheminform. 44: no-no. DOI: 10.1002/chin.201325221 |
0.534 |
|
| 2012 |
Mei TS, Kou L, Ma S, Engle KM, Yu JQ. Heterocycle Formation via Palladium-Catalyzed C-H Functionalization. Synthesis. 44: 1778-1791. PMID 27397938 DOI: 10.1055/S-0031-1289766 |
0.736 |
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| 2012 |
Mizuta S, Galicia-López O, Engle KM, Verhoog S, Wheelhouse K, Rassias G, Gouverneur V. Trifluoromethylation of allylsilanes under copper catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 8583-7. PMID 22692972 DOI: 10.1002/Chem.201201707 |
0.644 |
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| 2012 |
Baxter RD, Sale D, Engle KM, Yu JQ, Blackmond DG. Mechanistic rationalization of unusual kinetics in Pd-catalyzed C-H olefination. Journal of the American Chemical Society. 134: 4600-6. PMID 22324814 DOI: 10.1021/Ja207634T |
0.655 |
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| 2012 |
Engle KM, Mei TS, Wasa M, Yu JQ. Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions. Accounts of Chemical Research. 45: 788-802. PMID 22166158 DOI: 10.1021/Ar200185G |
0.804 |
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| 2012 |
Mei TS, Kou L, Ma S, Engle K, Yu JQ. Heterocycle formation via palladium-catalyzed C-H functionalization Synthesis (Germany). 44: 1778-1791. DOI: 10.1055/s-0031-1289766 |
0.67 |
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| 2012 |
Engle KM, Yu JQ, Davies HML, Xi Z, You SL, Shi ZJ. Transition Metal-Catalyzed C-H Functionalization: Synthetically Enabling Reactions for Building Molecular Complexity Organic Chemistry - Breakthroughs and Perspectives. 279-333. DOI: 10.1002/9783527664801.ch8 |
0.488 |
|
| 2011 |
Wasa M, Engle KM, Lin DW, Yoo EJ, Yu JQ. Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. Journal of the American Chemical Society. 133: 19598-601. PMID 22059375 DOI: 10.1021/Ja207607S |
0.809 |
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| 2011 |
Engle KM, Thuy-Boun PS, Dang M, Yu JQ. Ligand-accelerated cross-coupling of C(sp2)-H bonds with arylboron reagents. Journal of the American Chemical Society. 133: 18183-93. PMID 21913636 DOI: 10.1021/Ja203978R |
0.62 |
|
| 2011 |
Engle KM, Mei TS, Wang X, Yu JQ. Bystanding F+ oxidants enable selective reductive elimination from high-valent metal centers in catalysis. Angewandte Chemie (International Ed. in English). 50: 1478-91. PMID 21264991 DOI: 10.1002/Anie.201005142 |
0.701 |
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| 2011 |
Lu Y, Leow D, Wang X, Engle KM, Yu JQ. Hydroxyl-directed C-H carbonylation enabled by mono-N-protected amino acid ligands: An expedient route to 1-isochromanones Chemical Science. 2: 967-971. DOI: 10.1039/C0Sc00633E |
0.633 |
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| 2011 |
Engle KM, Mei T, Wang X, Yu J. Passive F+-Oxidationsmittel ermöglichen die selektive reduktive Eliminierung hochvalenter Metallzentren in der Katalyse Angewandte Chemie. 123: 1514-1528. DOI: 10.1002/Ange.201005142 |
0.635 |
|
| 2010 |
Wasa M, Engle KM, Yu JQ. Cross-coupling of C(sp)-H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis** Israel Journal of Chemistry. 50: 605-616. PMID 21552359 DOI: 10.1002/Ijch.201000038 |
0.742 |
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| 2010 |
Engle KM, Wang DH, Yu JQ. Ligand-accelerated C-H activation reactions: evidence for a switch of mechanism. Journal of the American Chemical Society. 132: 14137-51. PMID 20853838 DOI: 10.1021/Ja105044S |
0.718 |
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| 2010 |
Engle KM, Wang DH, Yu JQ. Constructing multiply substituted arenes using sequential palladium(II)-catalyzed C-H olefination. Angewandte Chemie (International Ed. in English). 49: 6169-73. PMID 20632344 DOI: 10.1002/Anie.201002077 |
0.731 |
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| 2010 |
Lu Y, Wang DH, Engle KM, Yu JQ. Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands. Journal of the American Chemical Society. 132: 5916-21. PMID 20359184 DOI: 10.1021/Ja101909T |
0.755 |
|
| 2010 |
Wasa M, Engle KM, Yu JQ. Pd(II)-catalyzed olefination of sp3 C-H bonds. Journal of the American Chemical Society. 132: 3680-1. PMID 20187642 DOI: 10.1021/Ja1010866 |
0.753 |
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| 2010 |
Wang DH, Engle KM, Shi BF, Yu JQ. Ligand-enabled reactivity and selectivity in a synthetically versatile aryl C-H olefination. Science (New York, N.Y.). 327: 315-9. PMID 19965380 DOI: 10.1126/Science.1182512 |
0.789 |
|
| 2010 |
Wasa M, Engle KM, Yu J. Cover Picture: Cross-Coupling of C(sp3)-H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis (Isr. J. Chem. 5-6/2010) Israel Journal of Chemistry. 50: 537-537. DOI: 10.1002/Ijch.201090011 |
0.711 |
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| 2010 |
Wasa M, Engle KM, Yu JQ. Cross-coupling of C(sp3)-H bonds with organometallic reagents via Pd(II)/Pd(0) catalysis Israel Journal of Chemistry. 50: 605-616. DOI: 10.1002/ijch.201000038 |
0.688 |
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| 2009 |
Giri R, Shi BF, Engle KM, Maugel N, Yu JQ. Transition metal-catalyzed C-H activation reactions: diastereoselectivity and enantioselectivity. Chemical Society Reviews. 38: 3242-72. PMID 19847354 DOI: 10.1039/B816707A |
0.756 |
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| 2009 |
Wasa M, Engle KM, Yu JQ. Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds. Journal of the American Chemical Society. 131: 9886-7. PMID 19580277 DOI: 10.1021/Ja903573P |
0.739 |
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| 2009 |
Chen X, Engle KM, Wang DH, Yu JQ. Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality. Angewandte Chemie (International Ed. in English). 48: 5094-115. PMID 19557755 DOI: 10.1002/Anie.200806273 |
0.691 |
|
| 2009 |
Chen X, Engle K, Wang D, Yu J. Palladium(II)-katalysierte C-H-Aktivierung/C-C-Kreuzkupplung: Vielseitigkeit und Anwendbarkeit Angewandte Chemie. 121: 5196-5217. DOI: 10.1002/Ange.200806273 |
0.636 |
|
| 2007 |
Plass KE, Engle KM, Matzger AJ. Contrasting two- and three-dimensional crystal properties of isomeric dialkyl phthalates. Journal of the American Chemical Society. 129: 15211-7. PMID 18001022 DOI: 10.1021/Ja0744798 |
0.59 |
|
| 2006 |
Plass KE, Engle KM, Cychosz KA, Matzger AJ. Large-periodicity two-dimensional crystals by cocrystallization. Nano Letters. 6: 1178-83. PMID 16771576 DOI: 10.1021/Nl0605061 |
0.599 |
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