| Year |
Citation |
Score |
| 2024 |
Byeon H, Kim J, Lee MH, Jang HY. Ir(tri-N-heterocyclic carbene)-catalyzed upgrading of glycerol: C-C bond formation for the synthesis of α-hydroxy acids. Organic & Biomolecular Chemistry. PMID 38305776 DOI: 10.1039/d3ob02035e |
0.309 |
|
| 2021 |
Jang HY. Oxidative cross-coupling of thiols for S-X (X = S, N, O, P, and C) bond formation: mechanistic aspects. Organic & Biomolecular Chemistry. PMID 34596196 DOI: 10.1039/d1ob01368h |
0.313 |
|
| 2020 |
Cheong Y, Sung K, Park S, Jung J, Jang H. Valorization of Chemical Wastes: Ir(biscarbene)-Catalyzed Transfer Hydrogenation of Inorganic Carbonates Using Glycerol Acs Sustainable Chemistry & Engineering. 8: 6972-6978. DOI: 10.1021/Acssuschemeng.0C00050 |
0.374 |
|
| 2020 |
Cheong Y, Sung K, Kim J, Kim YK, Jang H. Highly Efficient Iridium‐Catalyzed Production of Hydrogen and Lactate from Glycerol: Rapid Hydrogen Evolution by Bimetallic Iridium Catalysts European Journal of Inorganic Chemistry. DOI: 10.1002/Ejic.202000670 |
0.413 |
|
| 2019 |
Cheong Y, Lee S, Hwang SJ, Yoon W, Yun H, Jang H. Ir(bis-NHC)-Catalyzed Direct Conversion of Amines to Alcohols in Aqueous Glycerol European Journal of Organic Chemistry. 2019: 1940-1943. DOI: 10.1002/Ejoc.201900042 |
0.325 |
|
| 2019 |
Park H, Bae J, Son S, Jang H. Multifunctionalization of Indoles: Synthesis of 3‐Iodo‐2‐sulfonyl Indoles Bulletin of the Korean Chemical Society. 40: 1128-1133. DOI: 10.1002/Bkcs.11882 |
0.354 |
|
| 2018 |
Hwang SJ, Shyam PK, Jang H. Synthesis of Vinyl Sulfones via I2
-mediated Alkene Sulfonylations with Thiosulfonates Bulletin of the Korean Chemical Society. 39: 535-539. DOI: 10.1002/Bkcs.11426 |
0.388 |
|
| 2017 |
Shyam P, Jang HY. Synthesis of Sulfones and Sulfonamides via Sulfinate Anions: Revisiting the Utility of Thiosulfonates. The Journal of Organic Chemistry. PMID 28078894 DOI: 10.1021/Acs.Joc.6B03016 |
0.404 |
|
| 2017 |
Shyam PK, Son S, Jang H. Copper-Catalyzed Sulfonylation of Alkenes and Amines by Using Thiosulfonates as a Sulfonylating Agent European Journal of Organic Chemistry. 2017: 5025-5031. DOI: 10.1002/Ejoc.201700971 |
0.478 |
|
| 2017 |
Cho YJ, Lim YN, Yoon W, Yun H, Jang H. Palladium-Bis(carbene) Catalysts for the Bisalkoxycarbonylation of Olefins to Succinic Diesters European Journal of Organic Chemistry. 2017: 1139-1142. DOI: 10.1002/Ejoc.201601546 |
0.379 |
|
| 2017 |
Noh H, Lee C, Jang H. Organocatalyzed α-Sulfenylation of Carbonyl Compounds UsingN-Formyl/Acyl Sulfenamides Bulletin of the Korean Chemical Society. 38: 389-391. DOI: 10.1002/Bkcs.11098 |
0.391 |
|
| 2016 |
Kim JH, Shyam PK, Kim MJ, Lee HJ, Lee JT, Jang HY. Enantioselective synthesis and antioxidant activity of 3,4,5-substituted piperidine derivatives. Bioorganic & Medicinal Chemistry Letters. PMID 27177825 DOI: 10.1016/J.Bmcl.2016.04.092 |
0.33 |
|
| 2016 |
Kang YW, Cho YJ, Han SJ, Jang HY. Tunable and Diastereoselective Brønsted Acid Catalyzed Synthesis of β-Enaminones. Organic Letters. PMID 26741050 DOI: 10.1021/Acs.Orglett.5B03445 |
0.386 |
|
| 2016 |
Choi YJ, Jang HY. Copper-Catalyzed A3-Coupling: Synthesis of 3-Amino-1,4-diynes European Journal of Organic Chemistry. 2016: 3047-3050. DOI: 10.1002/Ejoc.201600343 |
0.355 |
|
| 2016 |
Lim S, Lim YN, Jang HY. TBD/alkyl halide-catalyzed synthesis of cyclic carbonates from CO2 Bulletin of the Korean Chemical Society. 37: 608-611. DOI: 10.1002/Bkcs.10724 |
0.324 |
|
| 2016 |
Shyam PK, Kim YK, Lee C, Jang HY. Copper-Catalyzed Aerobic Formation of Unstable Sulfinyl Radicals for the Synthesis of Sulfinates and Thiosulfonates Advanced Synthesis and Catalysis. 358: 56-61. DOI: 10.1002/Adsc.201500785 |
0.372 |
|
| 2015 |
Lee C, Wang X, Jang HY. Copper-catalyzed oxidative N-S bond formation for the synthesis of N-sulfenylimines. Organic Letters. 17: 1130-3. PMID 25685885 DOI: 10.1021/Ol503760B |
0.421 |
|
| 2015 |
Kang YW, Cho YJ, Ko KY, Jang HY. Copper-catalyzed carbon-carbon bond cleavage of primary propargyl alcohols: β-carbon elimination of hemiaminal intermediates Catalysis Science and Technology. 5: 3931-3934. DOI: 10.1039/C5Cy00783F |
0.378 |
|
| 2015 |
Lee C, Lim YN, Jang HY. Copper-Catalyzed Synthesis of N-Formyl/Acylsulfenamides and -thiosulfonamides European Journal of Organic Chemistry. 2015: 5934-5938. DOI: 10.1002/Ejoc.201500857 |
0.435 |
|
| 2015 |
Lim S, Ji M, Wang X, Lee C, Jang HY. Copper-catalyzed cross-coupling of thiols, alcohols, and oxygen for the synthesis of esters European Journal of Organic Chemistry. 2015: 591-595. DOI: 10.1002/Ejoc.201403311 |
0.388 |
|
| 2015 |
Shyam PK, Lee C, Jang HY. Copper-catalyzed oxidative olefination of thiols using sulfones and phosphorous ylides Bulletin of the Korean Chemical Society. 36: 1824-1827. DOI: 10.1002/Bkcs.10347 |
0.395 |
|
| 2014 |
Kang YW, Choi YJ, Jang HY. Copper-catalyzed TEMPO addition to propargyl alcohols for the synthesis of vinylic alkoxyamines. Organic Letters. 16: 4842-5. PMID 25188041 DOI: 10.1021/Ol502341F |
0.438 |
|
| 2014 |
Wang X, Ji M, Lim S, Jang HY. Thiol as a synthon for preparing thiocarbonyl: aerobic oxidation of thiols for the synthesis of thioamides. The Journal of Organic Chemistry. 79: 7256-60. PMID 24993111 DOI: 10.1021/Jo501378V |
0.331 |
|
| 2014 |
Lim YN, Wang X, Park EJ, Jang HY. Direct coupling of Cs2CO3 and alcohols for the synthesis of dimethyl, diethyl, and various dialkyl carbonates Bulletin of the Korean Chemical Society. 35: 622-624. DOI: 10.5012/Bkcs.2014.35.2.622 |
0.339 |
|
| 2014 |
Lee HJ, Shyam PK, Yoon W, Yun H, Jang HY. Diastereo- and enantioselective synthesis of hexasubstituted cyclohexanes via a metal-organocatalytic quadruple cascade sequence Synthesis (Germany). 46: 1329-1333. DOI: 10.1055/S-0033-1341103 |
0.429 |
|
| 2014 |
Kang YW, Jang HY. NHC-catalyzed one-pot oxidation and oxidative esterification of allylic alcohols using TEMPO: The effect of alcohol additives Rsc Advances. 4: 44486-44490. DOI: 10.1039/C4Ra08133A |
0.373 |
|
| 2014 |
Ji M, Lim S, Jang HY. N-heterocyclic carbene-catalyzed oxidation of aldehydes for the synthesis of amides via phenolic esters Rsc Advances. 4: 28225-28228. DOI: 10.1039/C4Ra04012K |
0.396 |
|
| 2014 |
Ho XH, Jung WJ, Shyam PK, Jang HY. Copper-dienamine catalysis: γ-oxyamination of α,β- unsaturated aldehydes Catalysis Science and Technology. 4: 1914-1919. DOI: 10.1039/C4Cy00271G |
0.364 |
|
| 2014 |
Shyam PK, Jang H. Metal-Organocatalytic Tandem Azide Addition/Oxyamination of Aldehydes for the Enantioselective Synthesis of β-Amino α-Hydroxy Esters (Eur. J. Org. Chem. 9/2014) European Journal of Organic Chemistry. 2014: n/a-n/a. DOI: 10.1002/Ejoc.201490021 |
0.335 |
|
| 2014 |
Lim YN, Lee C, Jang HY. Metal-free synthesis of cyclic and acyclic carbonates from CO2 and alcohols European Journal of Organic Chemistry. 2014: 1823-1826. DOI: 10.1002/Ejoc.201400031 |
0.309 |
|
| 2014 |
Shyam PK, Jang HY. Metal-organocatalytic tandem azide addition/oxyamination of aldehydes for the enantioselective synthesis of β-amino α-hydroxy esters European Journal of Organic Chemistry. 2014: 1817-1822. DOI: 10.1002/Ejoc.201301915 |
0.378 |
|
| 2013 |
Wang X, Lim YN, Lee C, Ji M, Kang EJ, Jang HY. Carbon dioxide-mediated metal-free oxidation of allylic alcohols to esters Rsc Advances. 3: 24922-24926. DOI: 10.1039/C3Ra44875D |
0.313 |
|
| 2013 |
Ji M, Wang X, Lim YN, Kang YW, Jang HY. N-heterocyclic carbene catalysed oxidative coupling of aldehydes with alcohols/thiols and one-pot oxidation/esterification of allylic alcohols European Journal of Organic Chemistry. 7881-7885. DOI: 10.1002/Ejoc.201301337 |
0.406 |
|
| 2013 |
Kim JH, Park EJ, Lee HJ, Ho XH, Yoon HS, Kim P, Yun H, Jang HY. Tandem iminium/copper catalysis: Highly enantioselective synthesis of α,β-disubstituted aldehydes European Journal of Organic Chemistry. 4337-4344. DOI: 10.1002/Ejoc.201300333 |
0.385 |
|
| 2013 |
Wang X, Lim YN, Lee C, Jang HY, Lee BY. 1,5,7-triazabicyclo[4.4.0]dec-1-ene-mediated acetylene dicarboxylation and alkyne carboxylation using carbon dioxide European Journal of Organic Chemistry. 1867-1871. DOI: 10.1002/Ejoc.201201608 |
0.316 |
|
| 2012 |
Yoon HS, Ho XH, Jang J, Lee HJ, Kim SJ, Jang HY. N719 dye-sensitized organophotocatalysis: enantioselective tandem Michael addition/oxyamination of aldehydes. Organic Letters. 14: 3272-5. PMID 22681592 DOI: 10.1021/Ol3011858 |
0.402 |
|
| 2012 |
Wang X, Jang HY. All-purpose copper catalyst for coupling of ammonium salts and 1° and 2° amines with boronic acid Bulletin of the Korean Chemical Society. 33: 1785-1787. DOI: 10.5012/Bkcs.2012.33.5.1785 |
0.389 |
|
| 2012 |
Krische MJ, Jang HY. 4.6 C-C Bond Formation (Metal-Catalyzed Reductive Aldol Coupling) Comprehensive Chirality. 4: 100-121. DOI: 10.1016/B978-0-08-095167-6.00405-5 |
0.492 |
|
| 2012 |
Ho XH, Oh HJ, Jang HY. Multistep organocatalysis for the asymmetric synthesis of multisubstituted aldehydes from allylic alcohols European Journal of Organic Chemistry. 5655-5659. DOI: 10.1002/Ejoc.201200863 |
0.389 |
|
| 2012 |
Yoon HS, Kim JH, Kang EJ, Jang HY. Platinum-catalyzed cyclization of N-allyl carbamates for the synthesis of 5-vinyloxazolidinones European Journal of Organic Chemistry. 1901-1905. DOI: 10.1002/Ejoc.201101799 |
0.448 |
|
| 2011 |
Hong JT, Jang HY. Platinum-catalyzed diastereoselective intramolecular coupling of allyl halides and hydrazones. The Journal of Organic Chemistry. 76: 6877-82. PMID 21718025 DOI: 10.1021/Jo200993V |
0.43 |
|
| 2011 |
Lim YN, Kim HT, Yoon HS, Jang HY. Regio- and stereoselective reductive cyclization of 1,5-bisallenes under hydrogenation conditions Bulletin of the Korean Chemical Society. 32: 3117-3119. DOI: 10.5012/Bkcs.2011.32.8.3117 |
0.438 |
|
| 2011 |
Ho XH, Kang MJ, Kim SJ, Park ED, Jang HY. Green organophotocatalysis. TiO2-induced enantioselective α-oxyamination of aldehydes Catalysis Science and Technology. 1: 923-926. DOI: 10.1039/C1Cy00183C |
0.398 |
|
| 2011 |
Kim HT, Yoon HS, Jang WY, Kang YK, Jang HY. Experimental and theoretical investigation of hydrogenative cyclization of allenynes European Journal of Organic Chemistry. 3748-3754. DOI: 10.1002/Ejoc.201100280 |
0.439 |
|
| 2010 |
Hong JT, Kang MJ, Jang HY. Pt(II)-catalyzed cyclization of alkyne-aldehydes Bulletin of the Korean Chemical Society. 31: 2085-2087. DOI: 10.5012/Bkcs.2010.31.7.2085 |
0.506 |
|
| 2010 |
Ho XH, Mho SI, Kang H, Jang HY. Electro-organocatalysis: Enantioselective α-alkylation of aldehydes European Journal of Organic Chemistry. 4436-4441. DOI: 10.1002/Ejoc.201000453 |
0.392 |
|
| 2010 |
Hong JT, Wang X, Kim JH, Kim K, Yun H, Jang HY. Platinum(II)-catalyzed allylation of C=O and C=N bonds under hydrogenation conditions Advanced Synthesis and Catalysis. 352: 2949-2954. DOI: 10.1002/Adsc.201000648 |
0.466 |
|
| 2009 |
Lee H, Jang MS, Song YJ, Jang HY. Platinum-catalyzed reductive aldol and Michael reactions Bulletin of the Korean Chemical Society. 30: 327-333. DOI: 10.5012/Bkcs.2009.30.2.327 |
0.405 |
|
| 2009 |
Jang MS, Wang X, Jang WY, Jang HY. Pt(II)/SnX2 (X = Cl, Br)-catalyzed cyclization: Completely different reactivity of the platinum complex toward 1,6-haloenynes and 1,6-enynes Organometallics. 28: 4841-4844. DOI: 10.1021/Om9004884 |
0.398 |
|
| 2009 |
Shinde MP, Wang X, Kang EJ, Jang H. Platinum-Catalyzed Hydrogenative Cyclization of Yne-Enones, Yne-Aldehydes, and Yne-Dienes (Eur. J. Org. Chem. 35/2009) European Journal of Organic Chemistry. 2009: 6063-6063. DOI: 10.1002/Ejoc.200990099 |
0.446 |
|
| 2009 |
Shinde MP, Wang X, Kang EJ, Jang HY. Platinum-catalyzed hydrogenative cyclization of yne-enones, yne-aldehydes, and yne-dienes European Journal of Organic Chemistry. 6091-6094. DOI: 10.1002/Ejoc.200901005 |
0.484 |
|
| 2009 |
Bui NN, Ho XH, Mho SI, Jang HY. Organocatalyzed α-oxyamination of aldehydes using anodic oxidation European Journal of Organic Chemistry. 5309-5312. DOI: 10.1002/Ejoc.200900871 |
0.438 |
|
| 2008 |
Bui NN, Hong JT, Ho XH, Mho SI, Jang HY. Correlation of electrochemical characteristics and catalytic activity of Rh2(OAc)4 in the presence of various phosphines Bulletin of the Korean Chemical Society. 29: 1624-1626. DOI: 10.5012/Bkcs.2008.29.8.1624 |
0.311 |
|
| 2008 |
Song YJ, Yoo C, Hong JT, Kim SJ, Seung US, Jang HY. Nanocrystalline copper oxide(II)-catalyzed alkyne-azide cycloadditions Bulletin of the Korean Chemical Society. 29: 1561-1564. DOI: 10.5012/Bkcs.2008.29.8.1561 |
0.367 |
|
| 2008 |
Lee H, Jang MS, Hong JT, Jang HY. Platinum-catalyzed reductive coupling of activated alkenes under hydrogenation conditions Tetrahedron Letters. 49: 5785-5788. DOI: 10.1016/J.Tetlet.2008.07.117 |
0.453 |
|
| 2007 |
Jang HY, Hong JB, MacMillan DWC. Enantioselective organocatalytic singly occupied molecular orbital activation: The enantioselective α-enolation of aldehydes Journal of the American Chemical Society. 129: 7004-7005. PMID 17497866 DOI: 10.1021/Ja0719428 |
0.321 |
|
| 2007 |
Song YJ, Jung IG, Lee H, Lee YT, Chung YK, Jang HY. Cationic NHC-Pd (NHC = N-heterocyclic carbene) complex-catalyzed cycloisomerization of dienes Tetrahedron Letters. 48: 6142-6146. DOI: 10.1016/J.Tetlet.2007.06.162 |
0.318 |
|
| 2007 |
Na SJ, Lee BY, Bui NN, Mho Si, Jang HY. A new dirhodium tetraacetate carbenoid: Synthesis, crystal structure and catalytic application Journal of Organometallic Chemistry. 692: 5523-5527. DOI: 10.1016/J.Jorganchem.2007.09.004 |
0.308 |
|
| 2007 |
Krische MJ, Jang HY. Metal-catalyzed reductive carbocyclization (C=C, C=C, C=O bonds) Comprehensive Organometallic Chemistry Iii. 10: 493-536. |
0.43 |
|
| 2005 |
Jang HY, Hughes FW, Gong H, Zhang J, Brodbelt JS, Krische MJ. Enantioselective reductive cyclization of 1,6-enynes via rhodium-catalyzed asymmetric hydrogenation: C-C bond formation precedes hydrogen activation. Journal of the American Chemical Society. 127: 6174-5. PMID 15853314 DOI: 10.1021/Ja042645V |
0.67 |
|
| 2004 |
Jang HY, Krische MJ. Catalytic C-C bond formation via capture of hydrogenation intermediates. Accounts of Chemical Research. 37: 653-61. PMID 15379581 DOI: 10.1021/Ar020108E |
0.541 |
|
| 2004 |
Jang HY, Krische MJ. Rhodium-catalyzed reductive cyclization of 1,6-diynes and 1,6-enynes mediated by hydrogen: catalytic C-C bond formation via capture of hydrogenation intermediates. Journal of the American Chemical Society. 126: 7875-80. PMID 15212535 DOI: 10.1021/Ja048498I |
0.511 |
|
| 2004 |
Jang HY, Huddleston RR, Krische MJ. Hydrogen-mediated C-C bond formation: catalytic regio- and stereoselective reductive condensation of alpha-keto aldehydes and 1,3-enynes. Journal of the American Chemical Society. 126: 4664-8. PMID 15070383 DOI: 10.1021/Ja0316566 |
0.594 |
|
| 2004 |
Marriner GA, Garner SA, Jang HY, Krische MJ. Metallo-aldehyde enolates via enal hydrogenation: catalytic cross aldolization with glyoxal partners as applied to the synthesis of 3,5-disubstituted pyridazines. The Journal of Organic Chemistry. 69: 1380-2. PMID 14961698 DOI: 10.1021/Jo030310A |
0.746 |
|
| 2004 |
Jang HY, Krische MJ. Catalytic hydrogen-mediated cross-coupling of enones and carbonyl compounds: Aldol condensation by hydrogenation European Journal of Organic Chemistry. 3953-3958. DOI: 10.1002/Ejoc.200400270 |
0.559 |
|
| 2003 |
Huddleston RR, Jang HY, Krische MJ. First catalytic reductive coupling of 1,3-diynes to carbonyl partners: a new regio- and enantioselective C-C bond forming hydrogenation. Journal of the American Chemical Society. 125: 11488-9. PMID 13129338 DOI: 10.1021/Ja030415V |
0.587 |
|
| 2003 |
Jang HY, Huddleston RR, Krische MJ. A New catalytic C[bond]C bond-forming hydrogenation: reductive coupling of dienes and glyoxals under catalytic hydrogenation conditions. Angewandte Chemie (International Ed. in English). 42: 4074-7. PMID 12973774 DOI: 10.1002/Anie.200351986 |
0.531 |
|
| 2003 |
Jang HY, Huddleston RR, Krische MJ. Nucleophilic Activation of Enones via Homogeneous Catalytic Hydrogenation: Catalytic Reductive C-C Bond Formation Under Hydrogenation Conditions Chemtracts. 16: 554-559. |
0.536 |
|
| 2002 |
Jang HY, Huddleston RR, Krische MJ. Reductive generation of enolates from enones using elemental hydrogen: catalytic C-C bond formation under hydrogenative conditions. Journal of the American Chemical Society. 124: 15156-7. PMID 12487574 DOI: 10.1021/Ja021163L |
0.602 |
|
| 2002 |
Wang LC, Jang HY, Roh Y, Lynch V, Schultz AJ, Wang X, Krische MJ. Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)(2)-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): mechanism and partitioning of hydrometallative versus anion radical pathways. Journal of the American Chemical Society. 124: 9448-53. PMID 12167039 DOI: 10.1021/Ja020223K |
0.541 |
|
| 2002 |
Wang LC, Luis AL, Agapiou K, Jang HY, Krische MJ. Organocatalytic Michael cycloisomerization of bis(enones): the intramolecular Rauhut-Currier reaction. Journal of the American Chemical Society. 124: 2402-3. PMID 11890765 DOI: 10.1021/Ja0121686 |
0.697 |
|
| 2002 |
Roh Y, Jang HY, Lynch V, Bauld NL, Krische MJ. Anion radical chain cycloaddition of tethered enones: intramolecular cyclobutanation and Diels-Alder cycloaddition. Organic Letters. 4: 611-3. PMID 11843604 DOI: 10.1021/Ol0172065 |
0.474 |
|
| 2001 |
Park HJ, Han JW, Seo H, Jang HY, Chung YK, Suh J. Preparation and application of polymer-supported π-allylpalladium complex as a chiral catalyst in the asymmetric allylic alkylation Journal of Molecular Catalysis a: Chemical. 174: 151-157. DOI: 10.1016/S1381-1169(01)00198-4 |
0.374 |
|
| 2000 |
Jang HY, Seo H, Han JW, Chung YK. Role of the planar chirality of imine-phosphine hybrid ligands bearing chromium tricarbonyl in the palladium-catalyzed asymmetric allylic alkylation Tetrahedron Letters. 41: 5083-5087. DOI: 10.1016/S0040-4039(00)00778-4 |
0.385 |
|
| 1999 |
Han JW, Jang HY, Chung YK. Synthesis and use in palladium-catalyzed asymmetric allylic alkylation of new planar chiral chromium complexes of 1,2-disubstituted arenes having pyridine and aryl phosphine groups Tetrahedron Asymmetry. 10: 2853-2861. DOI: 10.1016/S0957-4166(99)00296-7 |
0.396 |
|
| 1999 |
Son SU, Jang HY, Han JW, Lee IS, Chung YK. New planar chiral P,N-ligands containing tricarbonyl(arene)chromium for enantioselective asymmetric hydroboration of styrenes Tetrahedron Asymmetry. 10: 347-354. DOI: 10.1016/S0957-4166(99)00005-1 |
0.373 |
|
| 1998 |
Son SU, Jang HY, Lee IS, Chung YK. Synthesis of planar chiral (1,2-disubstituted arene)chromium tricarbonyl compounds and their application in asymmetric hydroboration Organometallics. 17: 3236-3239. DOI: 10.1021/Om980228J |
0.394 |
|
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