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Honghe Wan

A new allenic Pauson-Khand cycloaddition for the preparation of α-methylene cyclopentenones
1995 · Joseph L. Kent, Honghe Wan, et al. · Tetrahedron Letters · 114
An Intramolecular Allenic [2 + 2 + 1] Cycloaddition
1998 · Kay M. Brummond, Honghe Wan, et al. · The Journal of Organic Chemistry · 83
Chiral Nonracemic α-Alkylidene and α-Silylidene Cyclopentenones from Chiral Allenes Using an Intramolecular Allenic Pauson−Khand-Type Cycloaddition
2002 · Kay M. Brummond, Angela D. Kerekes, et al. · The Journal of Organic Chemistry · 77
Benzo[d]imidazole inhibitors of Coactivator Associated Arginine Methyltransferase 1 (CARM1)—Hit to Lead studies
2009 · Honghe Wan, Tram Huynh, et al. · Bioorganic & Medicinal Chemistry Letters · 62
Identification of chemokine receptor CCR4 antagonist
2005 · Ashok V. Purandare, Aiming Gao, et al. · Bioorganic & Medicinal Chemistry Letters · 58
The allenic Pauson-Khand cycloaddition. Dependence in π-bond selectivity on substrate structure
1998 · Kay M. Brummond, Honghe Wan · Tetrahedron Letters · 53
Core exploration in optimization of chemokine receptor CCR4 antagonists
2006 · Ashok V. Purandare, Honghe Wan, et al. · Bioorganic & Medicinal Chemistry Letters · 44
Discovery of Potent and Orally Bioavailable Small Molecule Antagonists of Toll-like Receptors 7/8/9 (TLR7/8/9)
2020 · Christopher P. Mussari, Dharmpal S. Dodd, et al. · ACS Medicinal Chemistry Letters · 42
Discovery of a Highly Selective JAK2 Inhibitor, BMS-911543, for the Treatment of Myeloproliferative Neoplasms
2015 · Honghe Wan, Gretchen M. Schroeder, et al. · ACS Medicinal Chemistry Letters · 40
Improved conditions for converting sterically hindered amides to 1,5-disubstituted tetrazoles
2010 · Gretchen M. Schroeder, Sydney Marshall, et al. · Tetrahedron Letters · 21
Optimization of CCR4 antagonists: Side-chain exploration
2005 · Ashok V. Purandare, Honghe Wan, et al. · Bioorganic & Medicinal Chemistry Letters · 19
Identification of a potent and rapidly reversible inhibitor of the 20S-proteasome
2004 · Ashok V. Purandare, Honghe Wan, et al. · Bioorganic & Medicinal Chemistry Letters · 17
Structure-Based Design of Selective Janus Kinase 2 Imidazo[4,5-d]pyrrolo[2,3-b]pyridine Inhibitors
2015 · Amy C. Hart, Gretchen M. Schroeder, et al. · ACS Medicinal Chemistry Letters · 16
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Pyrrolo[1,2-f]triazines as JAK2 inhibitors: Achieving potency and selectivity for JAK2 over JAK3
2011 · Lalgudi S. Harikrishnan, Muthoni G. Kamau, et al. · Bioorganic & Medicinal Chemistry Letters · 16
Long-Acting Tumor-Activated Prodrug of a TGFβR Inhibitor
2021 · Yong Zhang, Karen E. Parrish, et al. · Journal of Medicinal Chemistry · 6
Substituted diaryl ether compounds as retinoic acid-related orphan Receptor-γt (RORγt) agonists
2021 · Zheming Ruan, Peter K. Park, et al. · Bioorganic & Medicinal Chemistry Letters · 6
Discovery of BMS-159, an Orally Active Imidazotriazine Pan-CK2 Inhibitor for the Treatment of Cancer
2026 · Christine M. Tarby, Amy Hart, et al. · ACS Medicinal Chemistry Letters · 1
Abstract DDT01-03: Discovery of BMS-911543, a highly selective JAK2 inhibitor, as a clinical candidate for the treatment of myeloproliferative disease and other malignancies
2011 · Ashok V. Purandare, Honghe Wan, et al. · Cancer Research · 1
ChemInform Abstract: Improved Conditions for Converting Sterically Hindered Amides to 1,5‐Disubstituted Tetrazoles.
2010 · Gretchen M. Schroeder, Sydney Marshall, et al. · ChemInform
Optimization of CCR4 Antagonists: Side‐Chain Exploration.
2006 · Ashok V. Purandare, Honghe Wan, et al. · ChemInform
Identification of a Potent and Rapidly Reversible Inhibitor of the 20S‐Proteasome.
2004 · Ashok V. Purandare, Honghe Wan, et al. · ChemInform
Chiral Nonracemic α‐Alkylidene and α‐Silylidene Cyclopentenones from Chiral Allenes Using an Intramolecular Allenic Pauson—Khand‐Type Cycloaddition.
2003 · Kay M. Brummond, Angela D. Kerekes, et al. · ChemInform
Works count: 22
Citation count: 676
H-index: 14
I10-index: 14
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