C. Niu

发表

Synthesis of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP)

C. Niu, Jun Li, T. Doyle, 1998 .

First generation 5-vinyl-3-pyridinecarbonitrile PKCtheta inhibitors.

D. Boschelli, Biqi Wu, Xiaoke Yang, 2009, Bioorganic & medicinal chemistry letters.

Acetylenic TACE inhibitors. Part 1. SAR of the acyclic sulfonamide hydroxamates.

R. Black, J. Skotnicki, J. Levin, 2003, Bioorganic & medicinal chemistry letters.

Novel (4-piperidin-1-yl)-phenyl sulfonamides as potent and selective human beta(3) agonists.

M. Malamas, R. Mulvey, A. Oliphant, 2001, Bioorganic & medicinal chemistry.

Optimization of 5-phenyl-3-pyridinecarbonitriles as PKCtheta inhibitors.

D. Boschelli, Biqi Wu, Xiaoke Yang, 2009, Bioorganic & medicinal chemistry letters.

Optimization of 5-vinylaryl-3-pyridinecarbonitriles as PKCtheta inhibitors.

D. Boschelli, Biqi Wu, Xiaoke Yang, 2010, Bioorganic & medicinal chemistry letters.

C-5 Substituted heteroaryl 3-pyridinecarbonitriles as PKCtheta inhibitors: Part I.

D. Boschelli, Biqi Wu, Xiaoke Yang, 2009, Bioorganic & medicinal chemistry letters.

Enantioselective Total Syntheses of [6R,7R] and [6S,7S] Tricyclic β-Lactams

C. Niu, Marvin J Miller, T. Pettersson, 1996 .

Asymmetric syntheses of β-lactams and determination of their absolute configuration

C. Niu, Marvin J Miller, 1995 .

Enantioselective Total Syntheses of (6R,7R) and (6S,7S) Tricyclic . beta.‐Lactams.

C. Niu, Marvin J Miller, T. Pettersson, 1996 .

Efficient synthesis of ribonucleotide reductase inhibitors 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) and 3-amino-4-methylpyridine-2-carboxaldehyde thiosemicarbazone (3-AMP) via palladium mediated cross-coupling reactions

C. Niu, Jun Li, T. Doyle, 1998 .

D-piece modifications of the hemiasterlin analog HTI-286 produce potent tubulin inhibitors.

F. Loganzo, G. Krishnamurthy, L. Greenberger, 2004, Bioorganic & medicinal chemistry letters.

Asymmetric Syntheses of β‐Lactams and Determination of Their Absolute Configuration.

C. Niu, Marvin J Miller, 1995 .

Rearrangement of 3-amido-1-hydroxyazetidin-2-ones

C. Niu, Xiaobing Li, Marvin J Miller, 1995 .

Porphyrin binding to DNA investigated by cyclodextrin supramolecular system

S. Shuang, C. Niu, Xiao‐dong Yang, 2002, Analytical and Bioanalytical Chemistry.

Stereoselective Syntheses of β-l-FD4C and β-l-FddC

C. Niu, Jun Li, T. Doyle, 1997 .

Absolute configurations of tubulin inhibitors taltobulin (HTI-286) and HTI-042 characterized by X-ray diffraction analysis and NMR studies.

R. Williamson, C. Niu, S. Ayral-Kaloustian, 2010, Bioorganic & medicinal chemistry letters.

Synthesis and biological activity of analogues of the antimicrotubule agent N, β, β-trimethyl-L-phenylalanyl-N1-[(1S, 2E)-3-carboxy-1-isopropylbut-2-enyl]-N1, 3 -dimethyl-L-valinamide (HTI-286)

R. Williamson, F. Loganzo, C. Discafani, 2004 .

Discovery of the catechol structural moiety as a Stat3 SH2 domain inhibitor by virtual screening.

Yongbo Hu, J. Gibbons, C. Niu, 2008, Bioorganic & medicinal chemistry letters.

Acetylenic TACE inhibitors. Part 1. SAR of the acyclic sulfonamide hydroxamates.

R. Black, J. Skotnicki, J. Levin, 2003, Bioorganic & medicinal chemistry letters.

Synthesis and biological activity of analogues of the antimicrotubule agent N,beta,beta-trimethyl-L-phenylalanyl-N(1)-[(1S,2E)-3-carboxy-1-isopropylbut-2-enyl]- N(1),3-dimethyl-L-valinamide (HTI-286).

R. Williamson, F. Loganzo, C. Discafani, 2004, Journal of medicinal chemistry.