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Showing results 1 to 5 of 5

1
A copper-mediated cross-coupling approach for the synthesis of 3-heteroaryl quinolone and related analogues

Shin, Sang Hye; Kim, Yechan; Kim, Kiho; Hong, Sungwoo, ORGANIC & BIOMOLECULAR CHEMISTRY, v.12, no.30, pp.5719 - 5726, 2014-08

2
Design, Synthesis, and Evaluation of 3,5-Disubstituted 7-Azaindoles as Trk Inhibitors with Anticancer and Antiangiogenic Activities

Hong, Seunghee; Kim, Jinhee; Seo, Ju Hyeon; Jung, Kyung Hee; Hong, Soon-Sun; Hong, Sungwoo, JOURNAL OF MEDICINAL CHEMISTRY, v.55, no.11, pp.5337 - 5349, 2012-06

3
Discovery of EGF Receptor Inhibitors That Are Selective for the d746-750/T790M/C797S Mutant through Structure-Based de Novo Design

Park, Hwangseo; Jung, Hoi Yun; Mah, Shinmee; Hong, Sungwoo, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.26, pp.7634 - 7638, 2017-06

4
Rh(III)-catalyzed 7-azaindole synthesis via C-H activation/annulative coupling of aminopyridines with alkynes

Kim, Yechan; Hong, Sungwoo, CHEMICAL COMMUNICATIONS, v.51, no.56, pp.11202 - 11205, 2015

5
Virtual screening and biochemical evaluation to identify new inhibitors of mammalian target of rapamycin (mTOR)

Park, Hwangseo; Choe, Hyeonjeong; Hong, Sungwoo, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.24, no.3, pp.835 - 838, 2014-02

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