Year |
Citation |
Score |
2020 |
Zhou M, Park S, Dang L. Dual reactivity of B(C6F5)3 enables the silylative cascade conversion of N-aryl piperidines to sila-N-heterocycles: DFT calculations Organic Chemistry Frontiers. 7: 944-952. DOI: 10.1039/C9Qo01437C |
0.371 |
|
2020 |
Kim E, Jeon HJ, Park S, Chang S. Double Hydroboration of Quinolines via Borane Catalysis: Diastereoselective One Pot Synthesis of 3‐Hydroxytetrahydroquinolines Advanced Synthesis & Catalysis. 362: 308-313. DOI: 10.1002/Adsc.201901050 |
0.446 |
|
2019 |
Chang S, Zhang J, Jung H, Kim DW, Park S. Sequential C-H Borylation and N-Demethylation of 1,1'-Biphenylamines: An Alternative Route to Polycyclic BN-Heteroarenes. Angewandte Chemie (International Ed. in English). PMID 30941843 DOI: 10.1002/Anie.201902499 |
0.477 |
|
2019 |
Park S. Catalytic Reduction of Cyclic Ethers with Hydrosilanes. Chemistry, An Asian Journal. PMID 30938932 DOI: 10.1002/Asia.201900330 |
0.346 |
|
2019 |
Chang S, Jeong E, Heo J, Park S. Alkoxide-Promoted Selective Hydroboration of N-Heteroarenes: Pivotal Roles of in situ Generated BH3 in the Dearomatization Process. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30882934 DOI: 10.1002/Chem.201901214 |
0.473 |
|
2019 |
Zhang J, Hazra CK, Park S, Chang S. Metal‐Free Carbocyclization of Homoallylic Silyl Ethers Leading to Cyclopropanes and Cyclobutanes Asian Journal of Organic Chemistry. 8: 1637-1640. DOI: 10.1002/Ajoc.201900270 |
0.445 |
|
2018 |
Zhang J, Park S, Chang S. Catalytic Access to Bridged Sila-N-Heterocycles from Piperidines via Cascade sp3 and sp2 C-Si Bond Formation. Journal of the American Chemical Society. PMID 30269485 DOI: 10.1021/Jacs.8B08733 |
0.485 |
|
2018 |
Zhang J, Park S, Chang S. Piers' borane-mediated hydrosilylation of epoxides and cyclic ethers. Chemical Communications (Cambridge, England). PMID 29901036 DOI: 10.1039/C8Cc03741H |
0.463 |
|
2018 |
Chang S, Kim E, Park S. Silylative Reductive Amination of a,b-Unsaturated Aldehydes: A Convenient Synthetic Route to b-Silylated Secondary Amines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29488264 DOI: 10.1002/Chem.201800958 |
0.468 |
|
2018 |
Hazra CK, Jeong J, Kim H, Baik MH, Park S, Chang S. Reductive Carbocyclization of Homoallylic Alcohols to syn- Cyclobutanes via Boron-Catalyzed Dual Ring-Closing Pathway. Angewandte Chemie (International Ed. in English). PMID 29327487 DOI: 10.1002/Anie.201713285 |
0.444 |
|
2017 |
Chang S, Zhang J, Park S. In Situ Generated Piers' Borane-Catalyzed Selective C-O Bond Cleavage of Sugars with Hydrosilanes. Angewandte Chemie (International Ed. in English). PMID 28901040 DOI: 10.1002/Anie.201708109 |
0.468 |
|
2017 |
Chang S, Park S. Catalytic Dearomatization of N-Heteroarenes with Silicon and Boron Compounds. Angewandte Chemie (International Ed. in English). PMID 28164423 DOI: 10.1002/Anie.201612140 |
0.454 |
|
2017 |
Gandhamsetty N, Park S, Chang S. Boron-Catalyzed Hydrogenative Reduction of Substituted Quinolines to Tetrahydroquinolines with Hydrosilanes Synlett. 28: 2396-2400. DOI: 10.1055/S-0036-1588442 |
0.488 |
|
2017 |
Chang S, Zhang J, Park S. In Situ Generated Piers' Borane‐Catalyzed Selective C‐O Bond Cleavage of Sugars with Hydrosilanes Angewandte Chemie. DOI: 10.1002/Ange.201708109 |
0.423 |
|
2017 |
Park S, Chang S. Katalytische Desaromatisierung von N-Heteroarenen mit Silicium- und Borverbindungen Angewandte Chemie. 129: 7828-7847. DOI: 10.1002/Ange.201612140 |
0.389 |
|
2016 |
Jeong J, Park S, Chang S. Iridium-catalyzed selective 1,2-hydrosilylation of N-heterocycles. Chemical Science. 7: 5362-5370. PMID 30155189 DOI: 10.1039/C6Sc01037G |
0.497 |
|
2016 |
Hazra CK, Gandhamsetty N, Park S, Chang S. Borane catalysed ring opening and closing cascades of furans leading to silicon functionalized synthetic intermediates. Nature Communications. 7: 13431. PMID 27892459 DOI: 10.1038/Ncomms13431 |
0.473 |
|
2016 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Asilar E, Bergauer T, Brandstetter J, Brondolin E, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, ... ... Park SK, et al. Measurement of differential cross sections for Higgs boson production in the diphoton decay channel in pp collisions at [Formula: see text]. The European Physical Journal. C, Particles and Fields. 76: 13. PMID 26855607 DOI: 10.1140/Epjc/S10052-015-3853-3 |
0.315 |
|
2015 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Park SK, et al. Measurement of the differential cross section for top quark pair production in pp collisions at [Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 542. PMID 26640401 DOI: 10.1140/Epjc/S10052-015-3709-X |
0.315 |
|
2015 |
Kim KW, Park SH, Oh DH, Lee SH, Lim KS, Joo K, Chun YS, Chang SI, Min KM, Kim JC. Ribonuclease 5 coordinates signals for the regulation of intraocular pressure and inhibits neural apoptosis as a novel multi-functional anti-glaucomatous strategy. Biochimica Et Biophysica Acta. PMID 26581172 DOI: 10.1016/j.bbadis.2015.11.005 |
0.303 |
|
2015 |
Gandhamsetty N, Park S, Chang S. Selective Silylative Reduction of Pyridines Leading to Structurally Diverse Azacyclic Compounds with the Formation of sp3 C-Si Bonds. Journal of the American Chemical Society. PMID 26580152 DOI: 10.1021/Jacs.5B09209 |
0.465 |
|
2015 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Park SK, et al. Measurements of the [Formula: see text][Formula: see text] production cross sections in the [Formula: see text] channel in proton-proton collisions at [Formula: see text] and [Formula: see text] and combined constraints on triple gauge couplings. The European Physical Journal. C, Particles and Fields. 75: 511. PMID 26549982 DOI: 10.1140/Epjc/S10052-015-3706-0 |
0.329 |
|
2015 |
Kim J, Park SW, Baik MH, Chang S. Complete Switch of Selectivity in the C-H Alkenylation and Hydroarylation Catalyzed by Iridium: The Role of Directing Groups. Journal of the American Chemical Society. PMID 26449465 DOI: 10.1021/Jacs.5B09824 |
0.365 |
|
2015 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Park SK, et al. Distributions of topological observables in inclusive three- and four-jet events in pp collisions at [Formula: see text][Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 302. PMID 26190937 DOI: 10.1140/Epjc/S10052-015-3491-9 |
0.307 |
|
2015 |
Gandhamsetty N, Jeong J, Park J, Park S, Chang S. Boron-Catalyzed Silylative Reduction of Nitriles in Accessing Primary Amines and Imines. The Journal of Organic Chemistry. PMID 26152758 DOI: 10.1021/Acs.Joc.5B00941 |
0.485 |
|
2015 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Park SK, et al. Constraints on parton distribution functions and extraction of the strong coupling constant from the inclusive jet cross section in pp collisions at [Formula: see text][Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 288. PMID 26146483 DOI: 10.1140/Epjc/S10052-015-3499-1 |
0.321 |
|
2015 |
Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Park SK, et al. Search for a standard model Higgs boson produced in association with a top-quark pair and decaying to bottom quarks using a matrix element method. The European Physical Journal. C, Particles and Fields. 75: 251. PMID 26097407 DOI: 10.1140/Epjc/S10052-015-3454-1 |
0.318 |
|
2015 |
Gandhamsetty N, Park J, Jeong J, Park SW, Park S, Chang S. Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines. Angewandte Chemie (International Ed. in English). 54: 6832-6. PMID 25907098 DOI: 10.1002/Anie.201502366 |
0.474 |
|
2015 |
Gwon D, Park S, Chang S. Dual role of carboxylic acid additive: mechanistic studies and implication for the asymmetric C–H amidation Tetrahedron. 71: 4504-4511. DOI: 10.1016/J.Tet.2015.02.065 |
0.452 |
|
2014 |
Gandhamsetty N, Joung S, Park SW, Park S, Chang S. Boron-catalyzed silylative reduction of quinolines: selective sp3 C-Si bond formation. Journal of the American Chemical Society. 136: 16780-3. PMID 25412033 DOI: 10.1021/Ja510674U |
0.466 |
|
2014 |
Gwon D, Lee D, Kim J, Park S, Chang S. Iridium(III)-catalyzed C-H amidation of arylphosphoryls leading to a P-stereogenic center. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 12421-5. PMID 25145858 DOI: 10.1002/Chem.201404151 |
0.467 |
|
2014 |
Figg TM, Park S, Park J, Chang S, Musaev DG. Comparative investigations of cp*-based group 9 metal-catalyzed direct C-H amination of benzamides Organometallics. 33: 4076-4085. DOI: 10.1021/Om5005868 |
0.474 |
|
2013 |
Bézier D, Park S, Brookhart M. Selective reduction of carboxylic acids to aldehydes catalyzed by B(C6F5)3. Organic Letters. 15: 496-9. PMID 23317512 DOI: 10.1021/Ol303296A |
0.323 |
|
2012 |
Park S, Brookhart M. Development and mechanistic investigation of a highly efficient iridium(V) silyl complex for the reduction of tertiary amides to amines. Journal of the American Chemical Society. 134: 640-53. PMID 22091749 DOI: 10.1021/Ja209567M |
0.346 |
|
2012 |
Park S, Kim BG, Göttker-Schnetmann I, Brookhart M. Redistribution of trialkyl silanes catalyzed by iridium silyl complexes Acs Catalysis. 2: 307-316. DOI: 10.1021/Cs200629T |
0.302 |
|
2011 |
Park S, Brookhart M. Hydrosilylation of epoxides catalyzed by a cationic η1- silane iridium(iii) complex Chemical Communications. 47: 3643-3645. PMID 21321708 DOI: 10.1039/C0Cc05714B |
0.309 |
|
2010 |
Park S, Brookhart M. Hydrosilation of Carbonyl-Containing Substrates Catalyzed by an Electrophilic η-Silane Iridium(III) Complex. Organometallics. 29: 6057-6064. PMID 21572562 DOI: 10.1021/Om100818Y |
0.325 |
|
2009 |
Takeuchi D, Fukuda Y, Park S, Osakada K. Cyclopolymerization of 9,9-diallylfluorene promoted by Ni complexes. Stereoselective formation of six- and five-membered rings during the polymer growth Macromolecules. 42: 5909-5912. DOI: 10.1021/Ma901069Q |
0.307 |
|
2007 |
Takeuchi D, Matsuura R, Park S, Osakada K. Cyclopolymerization of 1,6-heptadienes catalyzed by iron and cobalt complexes: synthesis of polymers with trans- or cis-fused 1,2-cyclopentanediyl groups depending on the catalyst. Journal of the American Chemical Society. 129: 7002-3. PMID 17497787 DOI: 10.1021/Ja0718568 |
0.303 |
|
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