Browsing byAuthorKIM TAE JUNG

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Showing results 1 to 30 of 39

Issue DateTitleAuthor(s)
-Amorphastilbol derived from Amorpha fruticosa : Total synthesis and biological evaluation of dual PPAR α/γ agonistKIM TAE JUNG; Lee Woo Jung; Jeong Kyu Hyuk; Choi Pil-ju; Kim, Su-Nam; Seokjoon Lee; Masaya Nakata; Ham, Jungyeob
-An improved approach for the synthesis of natural arylnaphthalene lactoe lignans via Hauser-Kraus naphthol formation strategyKIM TAE JUNG; Hwang Buyng-su; Masaya Nakata; Ham, Jungyeob
-Biological evaluation of sulforaphane analogues as protective agents against cisplatin induced cytotoxicity in kidney cellsMoon Sung Won; KIM TAE JUNG; Ham, Jungyeob; Jae Wook Lee
-Cultivation of microalgae species in mixed wastewater for biodiesel and ß-carotene productionPark Young Tae; Yun Hyun Shik; Ji, Min-Kyu; KIM TAE JUNG; Choi Jae Young; Ham, Jungyeob
-Development of Anti-Cancer agents from Natural Products using Potassium AryltrifluoroboratesKIM TAE JUNG; Tetsuhiro Ogura; Toyonobu Usuki; Ham, Jungyeob
-Development of Orthogonal Reaction of Potassium Haloaryltrifluoroborates정규혁; KIM TAE JUNG; Song Jungho; Ham, Jungyeob
-Efficient Regioselective one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ potassium arylethynyltrifluoroborates through Sonogashira ReactionChoi Pil-ju; Song Jung Ho; Lee Myeong Jae; KIM TAE JUNG; Sang Il Jeon; Ham, Jungyeob
-Efficient synthesis of natural arylnaphthalene lactone lignans via Hauser-Kraus ring formation strategyKIM TAE JUNG; Lee Yoonseo; Kim Kyung Min; Ham, Jungyeob
-Functionalization of Organotrifluoroborate via Heck ReactionSong Jung Ho; KIM TAE JUNG; Ju Hae Yun; Ham, Jungyeob
-Functionalization of Potassium Organotrifluoroborate containing Alkyne GroupSong Jungho; KIM TAE JUNG; KIM HEEJIN; Ham, Jungyeob
-Functionalization of Potassium Organotrifluoroborates via 1,3-Dipolar Cycloaddition ReactionKIM TAE JUNG; Song Jungho; Ham, Jungyeob
-Improved anticancer effect of the microwave-irradiation processing ginseng extract increased important ginsenosides (Rg3, Rk1, and Rg5)Ham, Jungyeob; Pilju Choi; Kim Kyu Sun; Hwang Buyng-su; KIM TAE JUNG
-Improved anticancer effect of the microwave-irradiation processing ginseng extract increased Rg3, Rk1, and Rg5 ginsenosidesHam, Jungyeob; Ki Sung Kang; Choi Pilju; Jun Teon Park; KIM TAE JUNG; Soon-Hye Park; Ho-kyong Kim
-Natural Products Based Drug Development: The Concept of Naturomimetic Approach MethodJeong Kyu Hyuk; KIM TAE JUNG; Ham, Jungyeob
-Naturomimetic Approach toward the Anti-cancer Drugs using Potassium AryltrifluoroboratesJeong Kyu Hyuk; KIM TAE JUNG; Ham, Jungyeob
-Naturomimetic Approach toward the Anticancer Drugs using Potassium AryltrifluoroboratesSong Jungho; KIM TAE JUNG; 정규혁; Lee Myeong Jae; Ham, Jungyeob
-One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated potassium arylethynyltrifluoroboratesJeong Kyu Hyuk; Song Jung Ho; KIM TAE JUNG; Ham, Jungyeob
-Potassium (1-Organo-1H-1,2,3-triazol-4-yl)trifluoroborates from Ethynyltrifluoroborate via Regioselective One-Pot Cu-Catalyzed ReactionJeong Kyu Hyuk; KIM TAE JUNG; Song Jung Ho; Yong-Joo Kim; Ham, Jungyeob
-Potassium (1-Organo-1H-1,2,3-triazol-4-yl)trifluoroborates from Ethynyltrifluoroborate via Regioselective One-Pot CuAAC ReactionJeong Kyu Hyuk; KIM TAE JUNG; Song Jung Ho; Kim Yong-Joo; Ham, Jungyeob
-Potassium alkenylaryltrifluoroborates from haloaryltrifluoroborates via Mizoroki-Heck reactionKIM TAE JUNG; Jeong Kyu Hyuk; Song Jung Ho; Ham, Jungyeob
-Potassium(1-Organo-1H-1,2,3-triazol-4-yl)trifluoroborates from Ethynyltrifluroborate via Regioselective One-Pot CuAAC ReactionLee yoon seo; kim gyu sun; Choi Pilju; KIM TAE JUNG; Ham, Jungyeob
-Preparation of 1,4-disubstituted 1,2,3-triazoles from in situ generated potassium arylethynyltrifluoroboratesJeong Kyu Hyuk; Kim young seok; Kwantae Kim; KIM TAE JUNG; Ham, Jungyeob
-Regioselective one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated potassium arylethynyltrifluoroboratesChoi Pil-ju; Song Jung Ho; Lee Myeong Jae; KIM TAE JUNG; Ham, Jungyeob
-Studies toward the total synthesis of Octa-substituted Cyclopentane Natural Product, PactamycinKIM TAE JUNG; Yoko Saikawa; Masaya Nakata; Ham, Jungyeob
-Studies toward the total synthesis of pactamycinKIM TAE JUNG; So Matsudaira; Shinji Hirota; Shohei Matsushita; Tsuyoshi Doi; Yoko Saikawa; Ham, Jungyeob; Masaya Nakata
-Studies toward the total synthesis of pactamycin, multi-functionalized aminocyclitol natural productKIM TAE JUNG; Masaya Nakata; Ham, Jungyeob
-Studies toward the total synthesis of pactamycin, octa-substituted aminocyclitol natural productKIM TAE JUNG; Lee Yoonseo; Noh TaeSub; Masaya Nakata; Ham, Jungyeob
-Synthesis of Bioactive Natural Products and its derivatives using Naturomimetics Approach MethodKIM TAE JUNG; 정규혁; Ham, Jungyeob
-Synthesis of Biological Active Natural Product and its Derivatives via Suzuki-Miyaura Cross-Coupling Reaction정규혁; KIM TAE JUNG; Song Jungho; Ham, Jungyeob
-Synthesis of Regioselective Functionalized Organotrifluoroborates via 1,3-Dipolar Cycloaddition ReactionSong Jungho; KIM TAE JUNG; Ham, Jungyeob

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