| 2020-12 | 2-Anilinoquinoline based arylamides as broad spectrum anticancer agents with B-RAFV600E/C-RAF kinase inhibitory effects: Design, synthesis, in vitro cell-based and oncogenic kinase assessments | 금교창; 김은경; 이준석; 마무눌 하크; 신상철; Ashraf Kareem Awad Mohammed Eldamasy; 박정우 |
| 2010-11-24 | 2-피롤리돈기를 포함하는 옥사졸리디논 유도체 또는 이의 약학적으로 허용 가능한 염 및 이들의 제조방법 | 강순방; 금교창; 김유승; 김은경; 바타라이 디팍; 배애님; 서선희 |
| 1999-01-18 | 7-아미노데스아세톡시세팔로스포린산 유도체의 제조방법 | 강순방; 금교창; 김유승; 배애님; 조상원 |
| 2003-04 | A facile synthesis of 2,5-diketopiperazines based on isocyanide chemistry. | 조상원; 금교창; 강순방; 김유승; 한소엽 |
| 2000-03 | A facile synthesis of 7-amino-3-desacetoxycephalosporanic acid derivatives by indium-mediated reduction of 3-iodomethylcephems in aqueous media | 채형선; 조상원; 금교창; 강순방; 배애님; 김유승 |
| 1998-01 | A facile synthesis of N-carbamoylmethyl-α-aminobutyrolactones by the ugi multicomponent condensation reaction | 박수정; 금교창; 강순방; 고훈영; 김유승; 이덕형 |
| 1999-01 | A new direct allylation of the aromatic compounds with allylic chlorides catalyzed by indium metal | 임환정; 금교창; 강순방; 김유승; 정봉영 |
| 1998-10 | A new friedel-craft type allylation of aromatic compounds catalyzed by indium | 김유승; 임환정; 금교창; 강순방; 정봉영 |
| 1992-01 | A new peptide bond surrogate | 김병현; 정용준; 금교창; 김자헌; 김기문 |
| 1997-01 | A new route to quinolone and indole skeletones via ketone- and ester-imide cyclodehydration reactions | 김근철; 금교창 |
| 1998-04 | A new synthesis of α -aminobutyrolactone derivatives by ugi-five-component reaction | 김유승; 박수정; 채형선; 금교창; 이덕형 |
| 1999-04 | A new synthesis of α -aminovalerolactone derivatives by the ugi-five-component reaction | 김영배; 금교창; 강순방; 이덕형; 고훈형; 김유승 |
| 2003-07 | A novel indium mediated reaction of aldehyde with alkyl 4-bromocrotonate. | 장택수; 금교창; 강순방; 정봉영; 김유승 |
| 2018-07 | A novel tropomyosin-related kinase A inhibitor, KK5101 to treat pancreatic cancer | 배애님; 금교창; 가디 장데부 고라크스나트; 이주현; 아쉬라프 카림; Zhenghuan Fang; 한보름; 정경희; 김수정; Hong Hua Yan; 박정희; 이지은; 강여울; 홍순선 |
| 1999-01 | A Pd-catalyzed double coupling reaction to 4,5-disubstituted imidazole alkynes | 김건철; 강선화; 류영화; 금교창; 서명준 |
| 1994-01 | A synthesis of ( ± )-supinidine via an intramolecular carbenoid-thioimide coupling reaction | 김건철; 강선화; 금교창 |
| 1996-01 | A synthetic route to a C2-symmetrical alkoxy-ketone | 김건철; 금교창 |
| 2015-05 | ABL kinase inhibitory and antiproliferative activity of novel picolinamide based benzothiazoles | 아쉬라프 카림; 조남철; 강순방; 배애님; 금교창 |
| 2011-06 | Aminoquinoline derivatives as potent hepatitis C virus inhibitors | 이주현; 유경호; 장승기; 김은경; 금교창 |
| 2003-11 | An efficient synthesis of 2,5-diketopiperazine derivatives by the Ugi four-center three-component reaction. | 조상원; 금교창; 강순방; So-Yeop Han; 김유승 |
| 2000-04 | An efficient synthesis of morpholin-2-one derivatives by the Ugi five-center-three-component reaction on one-pot procedure | 최은희; 김영배; 금교창; 강순방; 이덕형; 김유승 |
| 2001-12 | An efficient synthesis of morpholin-2-one derivatives using glycolaldehyde dimer by the Ugi multicomponent reaction | 김영배; 최은희; 금교창; 강순방; 이덕형; 고훈영; 김유승 |
| 2002-11 | An efficient synthesis of α-amino-δ-valerolactones by the ugi five-center three-component reaction | 김영배; 박수정; 금교창; 장민석; 강순방; 이덕형; 김유승 |
| 2000-02 | An efficient synthesis of α-amino-δ-valerolactones by the Ugi five-center-three-component reaction | 김영배; 박수정; 금교창; 강순방; 이덕형; 고훈영; 김유승 |
| 1998-01 | An Efficient Transformation to the Structure of (±)-Supinidine | 김건철; 금교창; 김희석 |
| 2013-11 | Aryl Biphenyl-3-ylmethylpiperazines as 5-HT7 Receptor Antagonists | 김지연; 김영재; 태진성; 염미영; 문봉진; Xi-Ping Huang; Bryan L. Roth; 이강호; 임혜원; 추일한; 정유훈; 금교창; 남길수; 추현아 |
| 1998-10 | Asymmetric reduction of pyrrolidine derivatives using bakers yeast | 김유승; 오희영; 금교창; 강순방; 정봉영 |
| 2001-04 | Baker51s yeast reduction of β-Keto-α-oximino-carbonyl compounds | 금교창; 강순방; 김유승 |
| 2005-12 | Chemo- and enantioselective reduction of β-keto-α-oximino compounds using bakers yeast | 강순방; 모길웅; 하경희; 금교창; 장민석; 정봉영; 한소엽; 김유승 |
| 2002-10 | Chemo- and enatioselective reduction of Keto-Oxime compounds with Baker's yeast | 금교창; 강순방; 모길웅; 정봉영; 김유승 |
