S. Jung

发表

A degradable polydopamine coating based on disulfide-exchange reaction.

I. Choi, Juno Lee, J. Choi, 2015, Nanoscale.

Synthesis and PTP1B inhibition of 1,2-naphthoquinone derivatives as potent anti-diabetic agents.

Sung Soo Kim, H. Cheon, Sung-Don Yang, 2002, Bioorganic & medicinal chemistry letters.

Protein Tyrosine Phosphatase 1B Inhibitors: Catechols

Sung Soo Kim, H. Cheon, Sung-Don Yang, 2003 .

Pyrazolidine derivatives with heteroaryl urea as dipeptidyl peptidase IV inhibitors.

Sung Soo Kim, H. Cheon, S. Rhee, 2005, Chemical & pharmaceutical bulletin.

Synthesis and DP-IV inhibition of cyano-pyrazoline derivatives as potent anti-diabetic agents.

Sung Soo Kim, H. Cheon, S. Rhee, 2004, Bioorganic & medicinal chemistry letters.

Further Understandings of Regio- and Stereoselectivity in the Diels-Alder Reaction: Diels-Alder Reaction of Allenic Ester with 4-(Bulky)alkyl-substituted 3-siloxy-1,3-butadiene

S. Jung, Sang Hee Kim, 2003 .

Isoxazolylpyrrolidinylpiperazine Ligands, a New Class for Dopamine D 3 and D 4 Receptor Antagonists

H. Koh, S. Jung, J. Kwak, 2012 .

Synthesis and Biological Evaluation of Focused Isoxazolylpiperidinylpiperazine Library for Dopamine D3 and D4 Receptor Antagonists.

H. Koh, A. Pae, W. Park, 2011 .

Asymmetric synthesis of chiral piperazinylpropylisoxazoline ligands for dopamine receptors.

H. Koh, Ji-Young Jung, S. Jung, 2007, European journal of medicinal chemistry.

Pharmacological actions of a novel and selective dopamine D3 receptor antagonist, KCH-1110.

Y. Cho, H. Koh, A. Pae, 2003, Pharmacological research.

The Ratio Between the Percentage of Lymphocytes and Glucose Levels in Pericardial Fluid as a Method to Diagnose Tuberculous Pericarditis

S. Jung, S. Yoon, Tae Jin Kim, 2012 .

Solution-phase combinatorial synthesis of isoxazolines and isoxazoles using [2+3] cycloaddition reaction of nitrile oxides

Y. Cho, H. Koh, A. Pae, 2001 .

Synthesis of Piperazinylalkylisoxazoline Analogues and Their Binding Affinities for Dopamine Receptor Subtypes

H. Koh, A. Pae, Ji-Young Jung, 2006 .

Cleavage of N—O Bonds by Samarium Diiodide: A New Entry to Chemoselective Methods for the Conversion of Isoxazolines to β‐Hydroxy Ketones.

H. Koh, S. Jung, Jie Eun Lee, 2010 .

A Practical and Convenient Procedure for the N‐Formylation of Amines Using Formic Acid.

S. Park, J. Ahn, Joong-Kwon Choi, 2002 .

A [(4 + 2) + (3 + 2)] approach to a forskolin intermediate; a further understanding of π-facial selection in Diels-Alder reactions

J. Springer, A. Kozikowski, S. Jung, 1988 .

Synthesis, biological evaluation and structural determination of beta-aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors.

Jie-Oh Lee, S. Kim, Sung Soo Kim, 2007, Bioorganic & medicinal chemistry letters.

Synthetic Studies on the Stemona Alkaloids: Construction of BCD Tricyclic Ring Skeleton of Stenine Based on an IMDA/Beckmann Rearrangement Strategy.

H. Koh, S. Jung, H. Joo, 2000 .

Total synthesis of halichondrin B and norhalichondrin B

Craig J. Forsyth, Sun Ho Jung, Francis G. Fang, 1992 .

Synthetic Studies towards Halichondrins: Synthesis of the C.27–C.38 Segment

C. Forsyth, Y. Kishi, S. Jung, 1992 .

TBSOTf-assisted three component coupling of epoxides, THF, and ylides derived from the phosphoniosilylation products of enones and α,β-unsaturated lactones

Jung Hyun Kim, S. Jung, 2007 .

Transannular Diels-Alder reaction of a macrocyclic triene, (E,E,E)-13-trideca-2,8,10-trienolactone

Y. Lee, H. Park, S. Jung, 1995 .

A useful approach to tricyclic compounds and medium ring diketones through the phosphoniosilylation reaction.

A. Kozikowski, S. Jung, 1986 .

Synthetic Studies Towards Halichondrins: Synthesis of the Left Half of Halichondrins

C. Forsyth, Y. Kishi, S. Jung, 1992 .

Indenone Derivatives: A Novel Template for Peroxisome Proliferator-Activated Receptor γ (PPARγ) Agonists

Seung Jun Kim, W. Jung, H. Cheon, 2006 .

BF3-OEt2-Mediated Ring Opening of Oxetanes with Ylides Derived from the Phosphoniosilylation Products of Enones

S. Jung, S. Jang, 2010 .

A Practical Procedure for the Preparation of (1E,3E)‐5‐Alkoxy‐1‐siloxy‐ 1,3‐dienes.

C. Cheong, S. Jung, Mun-Su Yeo, 2010 .

A Facile and Green Protocol for Nucleophilic Substitution Reactions of Sulfonate Esters by Recyclable Ionic Liquids [bmim][X]

Yajun Liu, Junghyun Chae, S. Jung, 2012, Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry.

Synthesis and structure-activity relationship of novel indene N-oxide derivatives as potent peroxisome proliferator activated receptor γ (PPARγ) agonists

H. Cheon, S. Rhee, J. Ahn, 2007 .

A Case of Poncet's Disease in a Patient with Pulmonary Tuberculosis Accompanying Erythema Nodosum.

S. K. Lee, S. Jung, Tae Jin Kim, 2011 .

Synthesis of Piperazinylalkylisoxazoline Analogues and Their Binding Affinities for Dopamine Receptor Subtypes.

H. Koh, A. Pae, Ji-Young Jung, 2007 .

Production of Alternan by Leuconostoc mesenteroides CBI-110

S. Jung, Ho-Kwon Jung, Hong-seok Lee, 1999 .

Facile Preparation of Alkylidenesuccinimides from Maleimides via the Phosphoniosilylation Process

Jung Hyun Lee, Jung Hyun Kim, S. Jung, 2004 .

Phosphoniosilylation: an efficient and practical method for the β-functionalization of enones

A. Kozikowski, S. Jung, 1986 .

Indenone derivatives: a novel template for peroxisome proliferator-activated receptor gamma (PPARgamma) agonists.

W. Jung, H. Cheon, S. Rhee, 2006, Journal of medicinal chemistry.