Jin Hyo Kim

Dr. Jin Hyo Kim

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2015 in Chemosphere
Verified
Journal Article
Closed access
JKJin Hyo Kim
Jin Hyo Kim
YOYong Sik Ok
Yong Sik Ok
GCGeun-Hyoung Choi
Geun-Hyoung Choi
BPByung-Jun Park
Byung-Jun Park

31 October 2019 in Applied Biological Chemistry
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Journal Article
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HSHyeon Jeong Seong
Hyeon Jeong Seong
SKSeong Woo Kwon
Seong Woo Kwon
DSDong-Cheol Seo
Dong-Cheol Seo
JKJin Hyo Kim
Jin Hyo Kim
YJYu-Sin Jang
Yu-Sin Jang
Fluorine-containing compounds are widely used because they have properties required in textiles and coatings for electronic, automotive, and outdoor products. However, fluorinated compounds do not easily break down in nature, which has resulted in their accumulation in the environment as well as the human body. Recently, the enzymatic defluorination of fluorine-containing compounds has gained increasing attention. Here, we review the enzymatic defluorination reactions of fluorinated compounds. Furthermore, we review the enzyme engineering strategies for cleaving C–F bonds, which have the highest dissociation energy found in organic compounds.

17 March 2023 in Scientific Reports
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Journal Article
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JBJi-Yeon Bae
Ji-Yeon Bae
DLDeuk-Yeong Lee
Deuk-Yeong Lee
KOKyeong-Yeol Oh
Kyeong-Yeol Oh
DJDong-Kyu Jeong
Dong-Kyu Jeong
DLDong-Yeol Lee
Dong-Yeol Lee
JKJin Hyo Kim
Jin Hyo Kim
Pesticide residues in crops are widely monitored, and the residue reduction techniques at the post-harvest stage are important to maintain food safety. In dried crops, pesticide residues can be concentrated after dehydration, which increases concerns regarding residue risk. Therefore, the residue reduction effects of ultraviolet (UV), ozone, and photochemical advanced oxidative process (pAOP) were investigated for dried peppers at the post-harvest stage. UV254 treatment reduced 59.7% of the residue concentration on average, while UV360 showed a reduction of only 13.3% under 9.6 W m−2 of UV exposure for 24 h. Gaseous ozone treatments reduced the residue concentrations up to 57.9% on average. In contrast, the pAOP treatment reduced the concentration up to 97% and was superior to UV or ozone treatment alone. Increased drying temperature under pAOP condition resulted in higher reduction ratios at 40–80 °C. The pAOP conditions with 12 and 24 µmol/mol of ozone and UV254 irradiation for 24–48 h reduced the residue concentrations to 39–67%. Particularly, difenoconazole, fludioxonil, imidacloprid, and thiamethoxam residue concentrations were drastically reduced by over 50% under 12 µmol/mol ozone of the pAOP condition, while carbendazim, fluquinconazole, and pyrimethanil were relatively stable and their concentrations reduced below 50% under 24 µmol/mol ozone of the pAOP treatment. Various drying-related quality parameters of drying peppers such as water-soluble color, capsanthin, capsaicinoids, acid value, peroxide value, and thiobarbituric acid value were slightly altered, but not significantly, under 12 µmol/mol ozone of the pAOP condition, while the peroxide value was significantly altered under the higher ozone conditions. Therefore, pAOP treatment combined with gaseous ozone can be used for reducing residual pesticides in peppers without greatly reducing quality.

18 September 2020 in Environmental Geochemistry and Health
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Journal Article
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GCGeun-Hyoung Choi
Geun-Hyoung Choi
DLDeuk-Yeong Lee
Deuk-Yeong Lee
PBPennante Bruce-Vanderpuije
Pennante Bruce-Vanderpuije
ASAh-Reum Song
Ah-Reum Song
HLHyo-Sub Lee
Hyo-Sub Lee
JKJin Hyo Kim
Jin Hyo Kim

1 June 2004 in Organic Letters
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Journal Article
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JKJin Hyo Kim
Jin Hyo Kim
MLmarcus john curtis Long
marcus john curtis Long
JKJun Young Kim
Jun Young Kim
KPKi Hun Park
Ki Hun Park

1 January 1999 in Chemical Communications
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Journal Article
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WLWoo Song Lee
Woo Song Lee
KJKi Chang Jang
Ki Chang Jang
JKJin Hyo Kim
Jin Hyo Kim
KPKi Hun Park
Ki Hun Park
3-Acetyloxybut-1-enylamines 3–9 were easily transformed using iodine to pyrrolidine derivatives 3a–9a, precursors for aza sugars, via a diastereoselective iodoamidation.