Research output per year
Research output per year
Personal profile
In Korean
조찬식 교수(공과대학 응용화학과)
Education
o (1986) B.E., Kyungpook National University
o (1988) M.E., Kyungpook National University
o (1995) Dr. E., Kyoto University
o (1988) M.E., Kyungpook National University
o (1995) Dr. E., Kyoto University
Professional Experience
o (2017-Present) Professor, Kyungpook National University
o (2012-2017) Associate Professor, Kyungpook National University
o (2008-2012) Assistant Professor, Kyungpook National University
o (2012-2017) Associate Professor, Kyungpook National University
o (2008-2012) Assistant Professor, Kyungpook National University
Research Interests
Transition metal-catalyzed cross-coupling reaction, Synthesis of N-fused heterocycles, Organometallic chemistry, Heteroatom chemistry, Synthetic organic chemistry, Carbonylation, Homogeneous catalysis
Major Research Achievements
o Ruthenium-catalyzed regioselective α-alkylation of ketones: The first alkyl group transfer from trialkylamines to α C-atom of ketones
o Microwave-assisted cyclization under mildly basic conditions: Synthesis of 6H-benzo[c]chromen-6-ones and their 7,8,9,10-tetrahydro analogues
o Transition metal-free construction of trinuclear N-fused hybrid scaffolds by double nucleophilic aromatic substitution under microwave irradiation
o Construction of binuclear benzimidazole-fused quinazolinones and pyrimidinones using aryl isocyanates as building blocks by transition-metal-free C(sp2)-N coupling
o Base/DMSO-promoted synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines via C-C bond formation
o Microwave-assisted cyclization under mildly basic conditions: Synthesis of 6H-benzo[c]chromen-6-ones and their 7,8,9,10-tetrahydro analogues
o Transition metal-free construction of trinuclear N-fused hybrid scaffolds by double nucleophilic aromatic substitution under microwave irradiation
o Construction of binuclear benzimidazole-fused quinazolinones and pyrimidinones using aryl isocyanates as building blocks by transition-metal-free C(sp2)-N coupling
o Base/DMSO-promoted synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines via C-C bond formation
Fingerprint
Dive into the research topics where Chan Sik Cho is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
Base/DMSO-Promoted Synthesis of Benzo[4,5]imidazo[2,1-a]isoquinolines via C−C Bond Formation
Lee, S. W., Dao, P. D. Q., Lim, H. J. & Cho, C. S., 8 Mar 2024, In: Advanced Synthesis and Catalysis. 366, 5, p. 1182-1188 7 p.Research output: Contribution to journal › Article › peer-review
-
Magnetic MOF-199-Catalyzed Synthesis of Benzo[4,5]imidazo[1,2-f]phenanthridines and Their Analogues by Tandem C(sp2)−C Coupling and Cyclization Followed by Aromatization
Kim, M. J., Lee, S. W., Dao, P. D. Q. & Cho, C. S., 4 Aug 2023, In: ChemistrySelect. 8, 29, e202300926.Research output: Contribution to journal › Article › peer-review
-
Recyclable Magnetic Cu-MOF-74-Catalyzed C(sp2)-N Coupling and Cyclization under Microwave Irradiation: Synthesis of Imidazo[1,2-c]quinazolines and Their Analogues
Lee, S. W., Dao, P. D. Q., Lim, H. J. & Cho, C. S., 9 May 2023, In: ACS Omega. 8, 18, p. 16218-16227 10 p.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Construction of trinuclear N-fused hybrid scaffolds by coupling and cyclization of 2-bromoaryl- and 2-bromovinylimidazoles with ureas under recyclable Cu/C–Al2O3 catalysis
Dao, P. D. Q., Park, S. T., Sohn, H. S., Yoon, N. S. & Cho, C. S., 29 Jan 2022, In: Tetrahedron. 106-107, 132613.Research output: Contribution to journal › Article › peer-review
5 Scopus citations -
Copper-Catalyzed Synthesis of 5-Arylindolo[1,2-c]quinazolin-6(5H)-ones from 2-(2-Bromoaryl)indoles and Aryl Isocyanates under Microwave Irradiation
Dao, P. D. Q. & Cho, C. S., 13 Jun 2022, In: European Journal of Organic Chemistry. 2022, 22, e202200479.Research output: Contribution to journal › Article › peer-review
4 Scopus citations