J. W. Jeong

发表

Total synthesis of (+)-pamamycin-607.

S. Kang, Y. Hwang, J. W. Jeong, 2001, Angewandte Chemie.

Design, synthesis, and evaluation of 2-aryl-7-(3',4'-dialkoxyphenyl)-pyrazolo[1,5-a]pyrimidines as novel PDE-4 inhibitors.

C. Park, Hyung Rae Kim, Z. No, 2010, Bioorganic & medicinal chemistry letters.

A stereocontrolled synthetic route to the C1C18 subunit of pamamycin-607

S. Kang, J. W. Jeong, 2002 .

Discovery of N-(1-Acryloylazetidin-3-yl)-2-(1H-indol-1-yl)acetamides as Covalent Inhibitors of KRASG12C.

R. Fucini, Andrew M. Sawayama, J. McCarter, 2019, ACS medicinal chemistry letters.

Discovery of a novel series of potent and orally bioavailable phosphoinositide 3-kinase γ inhibitors.

Charles R. Holst, J. Nuss, Xiang Wu, 2012, Journal of medicinal chemistry.

Discovery of a novel class of potent and orally bioavailable sphingosine 1-phosphate receptor 1 antagonists.

Aaron Shipway, L. Mattheakis, J. Nuss, 2012, Journal of medicinal chemistry.

A substrate mimetic approach for influenza neuraminidase inhibitors

B. Woo, Z. No, Joon Won Jeong, 2004 .

Total synthesis of natural (+)-lasonolide A.

S. Kang, C. Park, S. Kang, 2003, Angewandte Chemie.

A stereoselective synthesis of the C15–C25 subunit of (+)-lasonolide A

S. Kang, J. Youn, S. Kang, 2003 .

Total Synthesis of Natural (+)-Lasonolide A (I).

S. Kang, C. Park, S. Kang, 2004 .

Triazolium cyclodextrin click cluster-resin conjugate: an enrichment material for phosphatidylinositol (3,4,5)-triphosphate.

C. Lim, Sangho Park, H. Le, 2017, Chemical communications.