Hyun‐Joon Ha - Concepedia

Author

Hyun‐Joon Ha

Hankuk University of Foreign Studies ORCID

Also Known As

H. J. Ha, H.-J. HA, H.-J. Ha, H.J. Ha, H.‐J. HA, Ha, Hyun-Joon, Ha, Hyun-Joon;Yoon, Doo-Ha;Kang, Lae-Sung;Hong, Myeng-Chan;Lee, Won-Koo;, Hoa Hà Mai, Hojung Ha, Hongkyu Ha

270

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

Hankuk University of Foreign Studies Sogang University Ajou University Ghent University Yong In University

About

Hyun‐Joon Ha is an author at Hankuk University of Foreign Studies specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	23	39	1.3K
2	Natural Sciences	20	33	955
3	Medicine	14	19	560
4	Health Sciences	1	1	22
5	Allergy	1	1	20

Hyun‐Joon Ha

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
An Efficient Synthesis of Anilinobenzylphosphonates Hyun‐Joon Ha, Gong-Sil Nam Synthetic Communications Chemical EngineeringEngineeringOrganic ChemistryCatalysisEfficient Synthesis	1992	96
Efficient Synthesis of Enantiomerically Pure 2-Acylaziridines: Facile Syntheses of <i>N</i>-Boc-safingol, <i>N</i>-Boc-<scp>d</scp><i>-erythro</i>-sphinganine, and <i>N</i>-Boc-spisulosine from a Common Intermediate Jung Min Yun, Tae Bo Sim, Heung Sik Hahm, The Journal of Organic Chemistry	2003	91
A Novel Synthesis of 5-Functionalized Oxazolidin-2-ones from Enantiomerically Pure 2-Substituted <i>N</i>-[(<i>R</i>)-(+)-α-Methylbenzyl]aziridines Tae Bo Sim, Se Hun Kang, Kun Su Lee, The Journal of Organic Chemistry 5-Functionalized Oxazolidin-2-onesPure Oxazolidin-2-onesEnantioselective SynthesisMedicineDiversity-oriented Synthesis	2002	78
High radiochemical yield synthesis of 3′-deoxy-3′-[18F]fluorothymidine using (5′-O-dimethoxytrityl-2′-deoxy-3′-O-nosyl-β-D-threo pentofuranosyl)thymine and its 3-N-BOC-protected analogue as a labeling precursor Mikyung Yun, Seung Jun Oh, Hyun‐Joon Ha, Nuclear Medicine and Biology EngineeringFluorous SynthesisOrganic Chemistry3-N-boc-protected Analogue5′-O-dimethoxytrityl-2′-deoxy-3′-o-nosyl-β-d-threo Pentofuranosyl	2003	77
Synthesis and evaluation of sphingoid analogs as inhibitors of sphingosine kinases Jin‐Wook Kim, Yong-Woo Kim, Yuichi Inagaki, Bioorganic & Medicinal Chemistry Medicinal ChemistryBiochemistryNatural SciencesMedicineSphingoid Analogs	2005	74
Systematic Study of Halide‐Induced Ring Opening of 2‐Substituted Aziridinium Salts and Theoretical Rationalization of the Reaction Pathways Matthias D’hooghe, Şaron Çatak, Sonja Stanković, European Journal of Organic Chemistry Theoretical RationalizationEngineeringHeterocyclicBiochemistryNatural Sciences	2010	69
Synthesis of 99mTc-ciprofloxacin by different methods and its biodistribution Seung Jun Oh, Jin‐Sook Ryu, Joong Woo Shin, Applied Radiation and Isotopes Medicinal ChemistryPharmaceutical ScienceAntimicrobial ChemotherapyPharmacologyPharmaceutical Chemistry	2002	68
Novel Stereoselective Synthesis of Functionalized Oxazolidinones from Chiral Aziridines Chan Sun Park, Min Sung Kim, Tae Bo Sim, The Journal of Organic Chemistry High YieldsHeterocyclicMedicineNovel Stereoselective SynthesisOrganic Chemistry	2002	68
Selective Mono‐BOC Protection of Diamines Dae Woo Lee, Hyun‐Joon Ha, Won Koo Lee Synthetic Communications Inorganic ChemistryChemical EngineeringBoron NitrideEngineeringFacile Route	2007	65
Opposite Regiospecific Ring Opening of 2-(Cyanomethyl)aziridines by Hydrogen Bromide and Benzyl Bromide: Experimental Study and Theoretical Rationalization Şaron Çatak, Matthias D’hooghe, Toon Verstraelen, The Journal of Organic Chemistry Theoretical RationalizationEngineeringHeterocyclicBenzyl Bromide CaseBenzyl Bromide	2010	60

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