Shengkai Ko - Concepedia

Author

Shengkai Ko

National Taiwan Normal University

Also Known As

S Ko, S. Ko, Shengkai Ko, Sooil Ko

Publications

921

Citations

H-Index

Concepts

All Affiliations

National Taiwan Normal University National Health Research Institutes

About

Shengkai Ko is an author at National Taiwan Normal University specializing in chemistry, organic chemistry, and catalysis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	4	4	456
2	Medicine	1	1	24
3	Natural Sciences	1	1	231
4	Biomolecular Engineering	1	1	65
5	Cell Biology	1	1	24

Shengkai Ko

Publications

911

Citations

H-Index

Page 1

	Year	Citations
Molecular Iodine Catalyzed One‐Pot Synthesis of 4‐Substituted‐1,4‐dihydropyridine Derivatives via Hantzsch Reaction. Shengkai Ko, M. N. V. Sastry, Chun‐Chi Lin, ChemInform Abstract AlgebraAbstraction (Computer Science)Organic ChemistryHantzsch ReactionSynthesis Method	2005	277
Ceric Ammonium Nitrate (CAN) catalyzes the one-pot synthesis of polyhydroquinoline via the Hantzsch reaction Shengkai Ko, Ching‐Fa Yao Tetrahedron Chemical EngineeringBioorganic ChemistryEngineeringNatural SciencesOne-pot Synthesis	2006	231
Heterogeneous catalyst: Amberlyst-15 catalyzes the synthesis of 14-substituted-14H-dibenzo[a,j]xanthenes under solvent-free conditions Shengkai Ko, Ching‐Fa Yao Tetrahedron Letters Chemical EngineeringEngineeringAlkene MetathesisOrganic ChemistrySolvent-free Conditions	2006	148
CAN and iodine-catalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde Shengkai Ko, Chun‐Chi Lin, Zhijay Tu, Tetrahedron Letters β-Unsaturated KetoneEngineeringIodine-catalyzed ReactionCatalytic SynthesisOrganic Chemistry	2005	65
An Investigation of the Reaction of 2-Aminobenzaldehyde Derivatives with Conjugated Nitro-olefins: An Easy and Efficient Synthesis of 3-Nitro-1,2-dihydroquinolines and 3-Nitroquinolines Ming-Chung Yan, Zhijay Tu, Chun‐Chi Lin, The Journal of Organic Chemistry 2-Aminobenzaldehyde DerivativesUnique Rearrangement Products2-Aryl-3-nitro-1,2-dihydroquinolines 3PharmacologyOrganic Chemistry	2004	54
Identification of BPR3P0128 as an Inhibitor of Cap-Snatching Activities of Influenza Virus John Hsu, Jiann-Yih Yeh, Ta-Jen Lin, Antimicrobial Agents and Chemotherapy	2011	49
Novel 2‐step synthetic indole compound 1,1,3‐tri(3‐indolyl)cyclohexane inhibits cancer cell growth in lung cancer cells and xenograft models Ching‐Hsiao Lee, Ching‐Fa Yao, Sin‐Ming Huang, Cancer	2008	34
Synthesis and Evaluation of the Cytotoxicities of Tetraindoles: Observation that the 5-Hydroxy Tetraindole (SK228) Induces G<sub>2</sub>Arrest and Apoptosis in Human Breast Cancer Cells Wen‐Shan Li, Chie‐Hong Wang, Shengkai Ko, Journal of Medicinal Chemistry Medicinal Chemistry5-Hydroxy TetraindoleMedicineApoptosisCancer Cell Biology	2012	24
BPR1K653, a Novel Aurora Kinase Inhibitor, Exhibits Potent Anti-Proliferative Activity in MDR1 (P-gp170)-Mediated Multidrug-Resistant Cancer Cells Chun Hei Antonio Cheung, Wen‐Hsing Lin, John Tsu‐An Hsu, PLoS ONE	2011	17
One-pot synthesis of malononitriles by free radical reactions of ylidenemalononitrile with Et3B and iodoalkane in a water–ether biphase medium Zhijay Tu, Chun‐Chi Lin, Yaochung Jang, Tetrahedron Letters Chemical EngineeringEngineeringWater–ether Biphase MediumOne-pot SynthesisOrganic Chemistry	2006	12

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