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2025
Prior to KNU
Prior to KNU
[45] C–H amidation of 2-aryl azlactones under iridium(iii) catalysis: access to chiral amino acids.
[45] C–H amidation of 2-aryl azlactones under iridium(iii) catalysis: access to chiral amino acids.
Min Seo Park, Eunjae Chung, Neeraj Kumar Mishra, Sang Hoon Han, Sangil Han, Saegun Kim* and In Su Kim*
Chem. Commun., 2022, 58, 13365-13368.
[44] C−H Methylation of Iminoamido Heterocycles with Sulfur Ylides.
[44] C−H Methylation of Iminoamido Heterocycles with Sulfur Ylides.
Prithwish Ghosh, Na Yeon Kwon, Saegun Kim, Sangil Han, Suk Hun Lee, Won An, Neeraj Kumar Mishra, Soo Bong Han and In Su Kim*
Angew. Chem. Int. Ed. 2021, 60, 191–196.
[43] Ru(ii)-Catalyzed C–H addition and oxidative cyclization of 2-aryl quinazolinones with activated aldehydes.
[43] Ru(ii)-Catalyzed C–H addition and oxidative cyclization of 2-aryl quinazolinones with activated aldehydes.
Jin Ho Choi, Kunyoung Kim, Harin Oh, Sangil Han, Neeraj Kumar Mishra* and In Su Kim*
Org. Biomol. Chem., 2020, 18, 9611-9622 (selected as a Cover Page of OBC).
[42] C2-Selective C–H Methylation of Heterocyclic N-Oxides with Sulfonium Ylides.
[42] C2-Selective C–H Methylation of Heterocyclic N-Oxides with Sulfonium Ylides.
Won An, Su Bin Choi, Namhoon Kim, Na Yeon Kwon, Prithwish Ghosh, Sang Hoon Han, Neeraj Kumar Mishra, Sangil Han,* Sungwoo Hong* and In Su Kim*
Org. Lett. 2020, 22, 9004–9009.
[41] Deoxygenative Amination of Azine-N-oxides with Acyl Azides via [3 + 2] Cycloaddition.
[41] Deoxygenative Amination of Azine-N-oxides with Acyl Azides via [3 + 2] Cycloaddition.
Dongeun Kim, Prithwish Ghosh, Na Yeon Kwon, Sang Hoon Han, Sangil Han, Neeraj Kumar Mishra, Saegun Kim* and In Su Kim*
J. Org. Chem. 2020, 85, 2476–2485.
[40] Site-Selective C–H Alkylation of Diazine N-Oxides Enabled by Phosphonium Ylides.
[40] Site-Selective C–H Alkylation of Diazine N-Oxides Enabled by Phosphonium Ylides.
Prithwish Ghosh, Na Yeon Kwon, Sangil Han, Saegun Kim, Sang Hoon Han, Neeraj Kumar Mishra, Young Hoon Jung, Sang J. Chung* and In Su Kim*
Org. Lett. 2019, 21, 6488–6493.
[39] Synthesis of (2H)-Indazoles from Azobenzenes Using Paraformaldehyde as a One-Carbon Synthon.
[39] Synthesis of (2H)-Indazoles from Azobenzenes Using Paraformaldehyde as a One-Carbon Synthon.
Rina Chun, Saegun Kim, Sang Hoon Han, Sangil Han, Suk Hun Lee, Neeraj Kumar Mishra, Young Hoon Jung, Hyung Sik Kim and In Su Kim*
Adv. Synth. Catal. 2019, 361, 1617–1626.
[38] Reductive C2-Alkylation of Pyridine and Quinoline N-Oxides Using Wittig Reagents.
[38] Reductive C2-Alkylation of Pyridine and Quinoline N-Oxides Using Wittig Reagents.
Sangil Han, Prashant Chakrasali, Jihye Park, Hyunjung Oh, Saegun Kim, Kyuneun Kim, Ashok Kumar Pandey, Sang Hoon Han, Soo Bong Han* and In Su Kim*
Angew. Chem. Int. Ed. 2018, 57, 12737–12740.
[37] Synthesis of (2H)-Indazoles through Rh(III)-Catalyzed Annulation Reaction of Azobenzenes with Sulfoxonium Ylides.
[37] Synthesis of (2H)-Indazoles through Rh(III)-Catalyzed Annulation Reaction of Azobenzenes with Sulfoxonium Ylides.
Hyunjung Oh,† Sangil Han,† Ashok Kumar Pandey, Sang Hoon Han, Neeraj Kumar Mishra, Saegun Kim, Rina Chun, Hyung Sik Kim, Jihye Park* and In Su Kim*
J. Org. Chem. 2018, 83, 4070–4077.
[36] Ru(II)-Catalyzed C–H Aminocarbonylation of N-(Hetero)aryl-7-azaindoles with Isocyanates.
[36] Ru(II)-Catalyzed C–H Aminocarbonylation of N-(Hetero)aryl-7-azaindoles with Isocyanates.
Taejoo Jeong, Suk Hun Lee, Rina Chun, Sangil Han, Sang Hoon Han, Yeong Uk Jeon, Jihye Park, Takehiko Yoshimitsu, Neeraj Kumar Mishra* and In Su Kim*
J. Org. Chem. 2018, 83, 4641–4649.
[35] Cp*Rh(iii)-catalyzed C(sp3)–H alkylation of 8-methylquinolines in aqueous media.
[35] Cp*Rh(iii)-catalyzed C(sp3)–H alkylation of 8-methylquinolines in aqueous media.
Saegun Kim,‡Sangil Han,‡Jihye Park, Satyasheel Sharma, Neeraj Kumar Mishra, Hyunjung Oh, Jong Hwan Kwak and In Su Kim*
Chem. Commun. 2017, 53, 3006–3009 (This paper was selected as Cover Page).
[34] Site-Selective Rhodium(III)-Catalyzed C−H Amination of 7-Azaindoles with Anthranils: Synthesis and Anticancer Evaluation.
[34] Site-Selective Rhodium(III)-Catalyzed C−H Amination of 7-Azaindoles with Anthranils: Synthesis and Anticancer Evaluation.
Mijin Jeon, Jihye Park, Prasanta Dey, Yongguk Oh, Hyunjung Oh, Sangil Han, Sung Hee Um, Hyung Sik Kim, Neeraj Kumar Mishra* and In Su Kim*
Adv. Synth. Catal. 2017, 359, 3471–3478 (This paper was selected as Cover Page).
[33] C(sp3)–H amination of 8-methylquinolines with azodicarboxylates under Rh(iii) catalysis: cytotoxic evaluation of quinolin-8-ylmethanamines.
[33] C(sp3)–H amination of 8-methylquinolines with azodicarboxylates under Rh(iii) catalysis: cytotoxic evaluation of quinolin-8-ylmethanamines.
Taejoo Jeong, Neeraj Kumar Mishra, Prasanta Dey, Hyunjung Oh, Sangil Han, Suk Hun Lee, Hyung Sik Kim, Jihye Park* and In Su Kim*
Chem. Commun. 2017, 53, 11197–11200.
[32] Synthesis and anti-inflammatory evaluation of N-sulfonyl anthranilic acids via Ir(III)-catalyzed C–H amidation of benzoic acids.
[32] Synthesis and anti-inflammatory evaluation of N-sulfonyl anthranilic acids via Ir(III)-catalyzed C–H amidation of benzoic acids.
Sang Hoon Han, Hyo Sun Suh, Hyeim Jo, Yongguk Oh, Neeraj Kumar Mishra, Sangil Han, Hyung Sik Kim, Young Hoon Jung, Byung Mu Lee* and In Su Kim*
Bioorg. Med. Chem. Lett. 2017, 27, 2129–2134.
[31] Recent Advances in Catalytic C(sp2)–H Allylation Reactions.
[31] Recent Advances in Catalytic C(sp2)–H Allylation Reactions.
Neeraj Kumar Mishra, Satyasheel Sharma, Jihye Park, Sangil Han and In Su Kim*
ACS Catal. 2017, 7, 2821–2847.
[30] Site-selective Cp*Rh(iii)-catalyzed C–H amination of indolines with anthranils.
[30] Site-selective Cp*Rh(iii)-catalyzed C–H amination of indolines with anthranils.
Neeraj Kumar Mishra, Mijin Jeon, Yongguk Oh, Hyeim Jo, Jihye Park, Sangil Han, Satyasheel Sharma, Sang Hoon Han, Young Hoon Jung and In Su Kim*
Org. Chem. Front. 2017, 4, 241–249.
[29] Redox-Neutral Rh(III)-Catalyzed Olefination of Carboxamides with Trifluoromethyl Allylic Carbonate.
[29] Redox-Neutral Rh(III)-Catalyzed Olefination of Carboxamides with Trifluoromethyl Allylic Carbonate.
Jihye Park,† Sangil Han,† Mijin Jeon, Neeraj Kumar Mishra, Seok-Yong Lee, Jong Suk Lee, Jong Hwan Kwak, Sung Hee Um* and In Su Kim*
J. Org. Chem. 2016, 81, 11353–11359.
[28] Rhodium(III)-Catalyzed C(sp3)–H Alkylation of 8-Methylquinolines with Maleimides.
[28] Rhodium(III)-Catalyzed C(sp3)–H Alkylation of 8-Methylquinolines with Maleimides.
Sangil Han, Jihye Park, Saegun Kim, Suk Hun Lee, Satyasheel Sharma, Neeraj Kumar Mishra, Young Hoon Jung and In Su Kim*
Org. Lett. 2016, 18, 4666–4669.
[27] Synthesis of Succinimide-Containing Chromones, Naphthoquinones, and Xanthones under Rh(III) Catalysis: Evaluation of Anticancer Activity.
[27] Synthesis of Succinimide-Containing Chromones, Naphthoquinones, and Xanthones under Rh(III) Catalysis: Evaluation of Anticancer Activity.
Sang Hoon Han, Saegun Kim, Umasankar De, Neeraj Kumar Mishra, Jihye Park, Satyasheel Sharma, Jong Hwan Kwak, Sangil Han, Hyung Sik Kim* and In Su Kim*
J. Org. Chem. 2016, 81, 12416–12425.
[26] Site-Selective C–H Amidation of Azobenzenes with Dioxazolones under Rhodium Catalysis.
[26] Site-Selective C–H Amidation of Azobenzenes with Dioxazolones under Rhodium Catalysis.
Neeraj Kumar Mishra, Yongguk Oh, Mijin Jeon, Sangil Han, Satyasheel Sharma, Sang Hoon Han, Sung Hee Um and In Su Kim*
Eur. J. Org. Chem. 2016, 4976–4980.
[25] Ruthenium(II)- or Rhodium(III)-Catalyzed Grignard-Type Addition of Indolines and Indoles to Activated Carbonyl Compounds.
[25] Ruthenium(II)- or Rhodium(III)-Catalyzed Grignard-Type Addition of Indolines and Indoles to Activated Carbonyl Compounds.
Hyeim Jo, Jihye Park, Miji Choi, Satyasheel Sharma, Mijin Jeon, Neeraj Kumar Mishra, Taejoo Jeong, Sangil Han and In Su Kim*
Adv. Synth. Catal. 2016, 358, 2714–2720 (This paper was selected as Cover Page and as a Very Important Publication).
[24] Rhodium-Catalyzed Vinylic C–H Functionalization of Enol Carbamates with Maleimides.
[24] Rhodium-Catalyzed Vinylic C–H Functionalization of Enol Carbamates with Maleimides.
Satyasheel Sharma, Sang Hoon Han, Hyeim Jo, Sangil Han, Neeraj Kumar Mishra, Miji Choi, Taejoo Jeong, Jihye Park and In Su Kim*
Eur. J. Org. Chem. 2016, 3611–3618.
[23] Synthesis of Phthalides through Tandem Rhodium-Catalyzed C–H Olefination and Annulation of Benzamides.
[23] Synthesis of Phthalides through Tandem Rhodium-Catalyzed C–H Olefination and Annulation of Benzamides.
Neeraj Kumar Mishra, Jihye Park, Miji Choi, Satyasheel Sharma, Hyeim Jo, Taejoo Jeong, Sangil Han, Saegun Kim and In Su Kim*
Eur. J. Org. Chem. 2016, 3076–3083.
[22] Trifluoromethylallylation of Heterocyclic C–H Bonds with Allylic Carbonates under Rhodium Catalysis.
[22] Trifluoromethylallylation of Heterocyclic C–H Bonds with Allylic Carbonates under Rhodium Catalysis.
Miji Choi, Jihye Park, Satyasheel Sharma, Hyeim Jo, Sangil Han, Mijin Jeon, Neeraj Kumar Mishra, Sang Hoon Han, Jong Suk Lee and In Su Kim*
J. Org. Chem. 2016, 81, 4771–4778.
[21] Mild and Site-Selective Allylation of Enol Carbamates with Allylic Carbonates under Rhodium Catalysis.
[21] Mild and Site-Selective Allylation of Enol Carbamates with Allylic Carbonates under Rhodium Catalysis.
Satyasheel Sharma, Sang Hoon Han, Yongguk Oh, Neeraj Kumar Mishra, Sangil Han, Jong Hwan Kwak, Seok-Yong Lee, Young Hoon Jung and In Su Kim*
J. Org. Chem. 2016, 81, 2243–2251.
[20] Rhodium(III)-catalyzed heteroatom-directed C–H allylation with allylic phosphonates and allylic carbonates at room temperature.
[20] Rhodium(III)-catalyzed heteroatom-directed C–H allylation with allylic phosphonates and allylic carbonates at room temperature.
Hyeim Jo, Sangil Han, Jihye Park, Miji Choi, Sang Hoon Han, Taejoo Jeong, Seok-Yong Lee, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Tetrahedron 2016, 72, 571–578.
[19] Access to 3-Acyl-(2H)-indazoles via Rh(III)-Catalyzed C–H Addition and Cyclization of Azobenzenes with α-Keto Aldehydes.
[19] Access to 3-Acyl-(2H)-indazoles via Rh(III)-Catalyzed C–H Addition and Cyclization of Azobenzenes with α-Keto Aldehydes.
Taejoo Jeong, Sang Hoon Han, Sangil Han, Satyasheel Sharma, Jihye Park, Jong Suk Lee, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Org. Lett. 2016, 18, 232–235.
[18] Synthesis of N-Sulfonylamidated and Amidated Azobenzenes under Rhodium Catalysis.
[18] Synthesis of N-Sulfonylamidated and Amidated Azobenzenes under Rhodium Catalysis.
Sangil Han, Neeraj Kumar Mishra, Satyasheel Sharma, Jihye Park, Miji Choi, Seok-Yong Lee, Joa Sub Oh, Young Hoon Jung and In Su Kim*
J. Org. Chem. 2015, 80, 8026–8035.
[17] Rh(III)-Catalyzed C–H Amidation of Indoles with Isocyanates.
[17] Rh(III)-Catalyzed C–H Amidation of Indoles with Isocyanates.
Taejoo Jeong,†Sangil Han,†Neeraj Kumar Mishra, Satyasheel Sharma, Seok-Yong Lee, Joa Sub Oh, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
J. Org. Chem. 2015, 80, 7243–7250.
[16] Direct C–H alkylation and indole formation of anilines with diazo compounds under rhodium catalysis.
[16] Direct C–H alkylation and indole formation of anilines with diazo compounds under rhodium catalysis.
Neeraj Kumar Mishra, Miji Choi, Hyeim Jo, Yongguk Oh, Satyasheel Sharma, Sang Hoon Han, Taejoo Jeong, Sangil Han, Seok-Yong Lee and In Su Kim*
Chem. Commun. 2015, 51, 17229–17232.
[15] Rh(III)-Catalyzed Direct Coupling of Azobenzenes with α-Diazo Esters: Facile Synthesis of Cinnolin-3(2H)-ones.
[15] Rh(III)-Catalyzed Direct Coupling of Azobenzenes with α-Diazo Esters: Facile Synthesis of Cinnolin-3(2H)-ones.
Satyasheel Sharma, Sang Hoon Han, Sangil Han, Wontae Ji, Jongchan Oh, Seok-Yong Lee, Joa Sub Oh, Young Hoon Jung and In Su Kim*
Org. Lett. 2015, 17, 2852–2855.
[14] Rhodium(III)-Catalyzed Selective CH Cyanation of Indolines and Indoles with an Easily Accessible Cyano Source.
[14] Rhodium(III)-Catalyzed Selective CH Cyanation of Indolines and Indoles with an Easily Accessible Cyano Source.
Neeraj Kumar Mishra, Taejoo Jeong, Satyasheel Sharma, Youngmi Shin, Sangil Han, Jihye Park, Joa Sub Oh, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Adv. Synth. Catal. 2015, 357, 1293–1298.
[13] Rhodium-catalyzed mild and selective C–H allylation of indolines and indoles with 4-vinyl-1,3-dioxolan-2-one: facile access to indolic scaffolds with an allylic alcohol moiety.
[13] Rhodium-catalyzed mild and selective C–H allylation of indolines and indoles with 4-vinyl-1,3-dioxolan-2-one: facile access to indolic scaffolds with an allylic alcohol moiety.
Satyasheel Sharma, Youngmi Shin, Neeraj Kumar Mishra, Jihye Park, Sangil Han, Taejoo Jeong, Yongguk Oh, Youngil Lee, Miji Choi and In Su Kim*
Tetrahedron 2015, 71, 2435–2441 (This paper was selected as Cover Page).
[12] Direct and Site-Selective Palladium-Catalyzed C-7 Acylation of Indolines with Aldehydes.
[12] Direct and Site-Selective Palladium-Catalyzed C-7 Acylation of Indolines with Aldehydes.
Youngmi Shin, Satyasheel Sharma, Neeraj Kumar Mishra, Sangil Han, Jihye Park, Hyunji Oh, Jimin Ha, Hyunwu Yoo, Young Hoon Jung and In Su Kim*
Adv. Synth. Catal. 2015, 357, 594–600.
[11] Mild Rh(III)-Catalyzed C7-Allylation of Indolines with Allylic Carbonates.
[11] Mild Rh(III)-Catalyzed C7-Allylation of Indolines with Allylic Carbonates.
Jihye Park, Neeraj Kumar Mishra, Satyasheel Sharma, Sangil Han, Youngmi Shin, Taejoo Jeong, Joa Sub Oh, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
J. Org. Chem. 2015, 80, 1818–1827.
[10] Rh(III)-Catalyzed Oxidative Coupling of 1,2-Disubstituted Arylhydrazines and Olefins: A New Strategy for 2,3-Dihydro-1H-Indazoles.
[10] Rh(III)-Catalyzed Oxidative Coupling of 1,2-Disubstituted Arylhydrazines and Olefins: A New Strategy for 2,3-Dihydro-1H-Indazoles.
Sangil Han, Youngmi Shin, Satyasheel Sharma, Neeraj Kumar Mishra, Jihye Park, Mirim Kim, Minyoung Kim, Jinbong Jang and In Su Kim*
Org. Lett. 2014, 16, 2494–2497.
[9] Decarboxylative acylation of indolines with α-keto acids under palladium catalysis: a facile strategy for the synthesis of 7-substituted indoles.
[9] Decarboxylative acylation of indolines with α-keto acids under palladium catalysis: a facile strategy for the synthesis of 7-substituted indoles.
Minyoung Kim, Neeraj Kumar Mishra, Jihye Park, Sangil Han, Youngmi Shin, Satyasheel Sharma, Youngil Lee, Eui-Kyung Lee, Jong Hwan Kwak and In Su Kim*
Chem. Commun. 2014, 50, 14249–14252.
[8] Ru(II)-Catalyzed Selective C–H Amination of Xanthones and Chromones with Sulfonyl Azides: Synthesis and Anticancer Evaluation.
[8] Ru(II)-Catalyzed Selective C–H Amination of Xanthones and Chromones with Sulfonyl Azides: Synthesis and Anticancer Evaluation.
Youngmi Shin, Sangil Han, Umasankar De, Jihye Park, Satyasheel Sharma, Neeraj Kumar Mishra, Eui-Kyung Lee, Youngil Lee, Hyung Sik Kim and In Su Kim*
J. Org. Chem. 2014, 79, 9262–9271.
[7] Direct allylation of aromatic and α,β-unsaturated carboxamides under ruthenium catalysis.
[7] Direct allylation of aromatic and α,β-unsaturated carboxamides under ruthenium catalysis.
Mirim Kim, Satyasheel Sharma, Neeraj Kumar Mishra, Sangil Han, Jihye Park, Minyoung Kim, Youngmi Shin, Jong Hwan Kwak, Sang Hoon Han and In Su Kim*
Chem. Commun. 2014, 50, 11303–11306 (This paper was selected as Cover Page).
[6] Copper-Catalyzed Oxidative C–O Bond Formation of 2-Acyl Phenols and 1,3-Dicarbonyl Compounds with Ethers: Direct Access to Phenol Esters and Enol Esters.
[6] Copper-Catalyzed Oxidative C–O Bond Formation of 2-Acyl Phenols and 1,3-Dicarbonyl Compounds with Ethers: Direct Access to Phenol Esters and Enol Esters.
Jihye Park, Sang Hoon Han, Satyasheel Sharma, Sangil Han, Youngmi Shin, Neeraj Kumar Mishra, Jong Hwan Kwak, Cheong Hoon Lee, Jeongmi Lee and In Su Kim*
J. Org. Chem. 2014, 79, 4735–4742.
[5] Rh-catalyzed oxidative C2-alkenylation of indoles with alkynes: unexpected cleavage of directing group.
[5] Rh-catalyzed oxidative C2-alkenylation of indoles with alkynes: unexpected cleavage of directing group.
Satyasheel Sharma, Sangil Han, Youngmi Shin, Neeraj Kumar Mishra, Hyunji Oh, Jihye Park, Jong Hwan Kwak, Beom Soo Shin, Young Hoon Jung and In Su Kim*
Tetrahedron Lett. 2014, 55, 3014–3017.
[4] Rh-catalyzed oxidative C–C bond formation and C–N bond cleavage: direct access to C2-olefinated free (NH)-indoles and pyrroles.
[4] Rh-catalyzed oxidative C–C bond formation and C–N bond cleavage: direct access to C2-olefinated free (NH)-indoles and pyrroles.
Satyasheel Sharma, Sangil Han, Mirim Kim, Neeraj Kumar Mishra, Jihye Park, Youngmi Shin, Jimin Ha, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Org. Biomol. Chem. 2014, 12, 1703–1706.
[3] Direct access to isoindolines through tandem Rh(iii)-catalyzed alkenylation and cyclization of N-benzyltriflamides.
[3] Direct access to isoindolines through tandem Rh(iii)-catalyzed alkenylation and cyclization of N-benzyltriflamides.
Neeraj Kumar Mishra, Jihye Park, Satyasheel Sharma, Sangil Han, Mirim Kim, Youngmi Shin, Jinbong Jang, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Chem. Commun. 2014, 50, 2350–2352.
[2] Pd-Catalyzed Oxidative Coupling of Arene C–H Bonds with Benzylic Ethers as Acyl Equivalents.
[2] Pd-Catalyzed Oxidative Coupling of Arene C–H Bonds with Benzylic Ethers as Acyl Equivalents.
Sangil Han, Satyasheel Sharma, Jihye Park, Mirim Kim, Youngmi Shin, Neeraj Kumar Mishra, Jong Jin Bae, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
J. Org. Chem. 2014, 79, 275–284.
[1] Synthesis and C2-functionalization of indoles with allylic acetates under rhodium catalysis.
[1] Synthesis and C2-functionalization of indoles with allylic acetates under rhodium catalysis.
Mirim Kim, Jihye Park, Satyasheel Sharma, Sangil Han, Sang Hoon Han, Jong Hwan Kwak, Young Hoon Jung and In Su Kim*
Org. Biomol. Chem. 2013, 11, 7427–7434.
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