I. Kim

发表

A Convenient Synthesis of 5‐Methylbenzo[c]phenanthridin‐6(5H)‐one.

W. Cho, I. Kim, Sun-Ja Park, 2001 .

A critical structural determinant of opioid receptor interaction with phenolic 5-phenylmorphans.

K. Rice, R. Rothman, C. Dersch, 2004, Bioorganic & medicinal chemistry.

THE FIRST SUCCESSFUL INTRAMOLECULAR DIELS-ALDER REACTION LEADING TO A BACCATIN III CONSTRUCT BEARING OXYGEN FUNCTIONALITY AT C10

S. Danishefsky, S. D. Gala, T. Park, 1995 .

A Fully Synthetic Globo H Carbohydrate Vaccine Induces a Focused Humoral Response in Prostate Cancer Patients: A Proof of Principle.

H. Scher, W. Bornmann, S. Slovin, 1999, Angewandte Chemie.

Total Synthesis and Proof of Structure of a Human Breast Tumor (Globo-H) Antigen

J. Randolph, S. Danishefsky, M. Bilodeau, 1996 .

An optically active chromium(0)-complexed benzaldehyde in organic synthesis: A highly stereocontrolled asymmetric synthesis of (2R,3S)-(-)-N-benzoyl-3-phenylisoserine methyl ester, the taxol C-13 side chain analogue

C. Mukai, M. Hanaoka, I. Kim, 1992 .

Studies on total syntheses of antitumor styryllactones: Stereoselective total syntheses of (+)-goniofufurone, (+)-goniobutenolide A, and (−)-goniobutenolide B

C. Mukai, M. Hanaoka, M. Kido, 1996 .

Synthesis and pharmacological evaluation of 3-(3,4-dichlorophenyl)-1-indanamine derivatives as nonselective ligands for biogenic amine transporters.

J. Flippen-Anderson, K. Rice, R. Rothman, 2004, Journal of medicinal chemistry.

Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-phenylmorphans. Synthesis of a µ-agonist δ-antagonist and δ-inverse agonists

K. Rice, M. Aceto, L. Harris, 2007 .

Optically active tricarbonyl(η6-o-trimethylsilylbenzaldehyde)chromium(O) complexes in organic synthesis: a highly diastereoselective 1,3-dipolar cycloaddition with electron-rich olefins

W. Cho, C. Mukai, M. Hanaoka, 1993 .

Asymmetric aldol reaction : a highly Erythro-selective aldol reaction between tricarbonyl(O-trimethylsilylbenzaldehyde derivative)- chromium(0) complexes and cyclic silyl enol ethers

W. Cho, C. Mukai, M. Hanaoka, 1991 .

An optically active chromium(0)-complexed benzaldehyde derivative in organic synthesis: A highly stereocontrolled total synthesis of (+)-goniofufurone

C. Mukai, M. Hanaoka, I. Kim, 1993 .

Asymmetric Aldol Reaction: A Highly erythro‐Selective Aldol Reaction Between Tricarbonyl(o‐trimethylsilylbenzaldehyde derivative)chromium(0) Complexes and Cyclic Silyl Enol Ethers.

W. Cho, C. Mukai, M. Hanaoka, 1991 .

Highly stereocontrolled asymmetric syntheses of taxol and taxotère C-13 side chain analogues

C. Mukai, M. Hanaoka, I. Kim, 1993 .

On the importance of the stereochemistry at C10 in governing the feasibility of the intramolecular Diels-Alder route to baccatin III constructs: Surprising results in the 10R-9-deoxy series

S. Danishefsky, T. Park, I. Kim, 1995 .

Total synthesis of (′)-ceratopicanol

Minoru Kobayashi, C. Mukai, M. Hanaoka, 2002 .

New entry to the Pauson–Khand reaction: trimethylgermyl group at the triple bond terminus as a latent functional group

C. Mukai, Takashi Kozaka, I. Kim, 2004 .

Defining the Molecular Recognition of MBr1 (Human Breast Cancer) Antigen by the MBr1 Antibody through Probe Structures Prepared by Total Synthesis

S. Danishefsky, Shengle Zhang, P. Livingston, 1995 .

Trimethylgermyl group in Pauson–Khand reaction

C. Mukai, Takashi Kozaka, I. Kim, 2002 .

First total synthesis and structural elucidation of (−)-goniofupyrone

C. Mukai, M. Hanaoka, I. Kim, 1996 .

Immunization of Mice with a Fully Synthetic Globo H Antigen Results in Antibodies against Human Cancer Cells: A Combined Chemical—Immunological Approach to the Fashioning of an Anticancer Vaccine

S. Danishefsky, K. Lloyd, Shengle Zhang, 1997 .

Synthesis of π‐Extended Coumarins and Evaluation of Their Precursors as Reactive Fluorescent Probes for Mercury Ions

Dokyoung Kim, K. Ahn, I. Kim, 2012 .

Characterization of a mouse monoclonal IgG3 antibody to the tumor-associated globo H structure produced by immunization with a synthetic glycoconjugate

M. Breimer, S. Danishefsky, K. Lloyd, 1998, Glycoconjugate Journal.

Diaryldimethylpiperazine ligands with μ- and δ-opioid receptor affinity: Synthesis of (+)-4-[(αR)-α-(4-allyl-(2S, 5S)-dimethylpiperazin-1-yl)-(3-hydroxyphenyl)methyl]- N-ethyl-N-phenylbenzamide and (-)-4-[(αR)-α-(2S, 5S)-dimethylpiperazin-1-yl)-(3-hydroxyphenyl)methyl]-N-ethyl-N -phenylbenzamide

Judith L. Flippen-Anderson, Arthur E. Jacobson, Clifford George, 2003 .