W. Gu

发表

Synthesis of (S)-2-Boc-Amino-8-(R)-(tert-butyldimethylsilanyloxy) decanoic acid, a Precursor to the Unusual Amino Acid Residue of the Anticancer Agent Microsporin B.

R. Silverman, W. Gu, 2011, Tetrahedron letters.

Microsporins A and B: new histone deacetylase inhibitors from the marine-derived fungus Microsporum cf. gypseum and the solid-phase synthesis of microsporin A

P. Jensen, W. Fenical, R. Silverman, 2007 .

N-methylsansalvamide a peptide analogues. Potent new antitumor agents.

T. Adrian, G. Soff, R. Silverman, 2005, Journal of medicinal chemistry.

Isosteric replacements of the carboxylic acid of drug candidate VX-787: Effect of charge on antiviral potency and kinase activity of azaindole-based influenza PB2 inhibitors.

P. Charifson, Tiansheng Wang, E. Perola, 2015, Bioorganic & medicinal chemistry letters.

One‐Pot Synthesis of Highly Substituted Pyrroles by Three‐Component Reactions of Donor–Acceptor Cyclopropanes, Salicylaldehydes, and Ammonium Acetate

Cunde Wang, W. Gu, Siran Qian, 2018 .

Stereospecific total syntheses of proteasome inhibitors omuralide and lactacystin.

R. Silverman, W. Gu, 2011, The Journal of organic chemistry.

First asymmetric synthesis of chiral 1,4-benzodioxane lignans

A. Chan, W. Gu, Xiaobi Jing, 2000 .

First enantioselective syntheses of (2 R ,3 R )- and (2 S ,3 S )-3-(4-hydroxy-3-methoxyphenyl)-2-hydroxymethyl-1,4-benzodioxan-6-carbaldehyde

A. Chan, Xiaochuan Chen, W. Gu, 2000 .

A Convenient Stereoselective Synthesis of Isoamericanol a and Isoamericanin A

Tongxing Wu, X. She, W. Gu, 1999 .

A Convenient Synthesis of (±)-3-Methoxybenzodioxane-4,9,9′-triol Neolignan, and Methyl Ethers of Isoamericanol A and Isoamericanin A

Tongxing Wu, X. She, W. Gu, 1999 .

Study on the Total Synthesis of Neolignans(I): Synthesis of the Methyl Ethers of Americanin A and Americanol A

X. She, W. Gu, Xin-fu Pan, 1998 .

Inactivation of mitochondrial monoamine oxidase B by methylthio-substituted benzylamines.

R. Silverman, W. Gu, Xingliang Lu, 2003, Bioorganic & medicinal chemistry.

A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest.

T. Adrian, M. Talamonti, R. Silverman, 2006, Biochemical and biophysical research communications.

Design, synthesis and biological evaluation of potent NAD+-dependent DNA ligase inhibitors as potential antibacterial agents. Part I: aminoalkoxypyrimidine carboxamides.

F. Maltais, P. Charifson, Tiansheng Wang, 2012, Bioorganic & medicinal chemistry letters.

Discovery and Optimization of Pyrazole Amides as Inhibitors of ELOVL1.

Kevin J. Gagnon, F. Maltais, P. Charifson, 2021, Journal of medicinal chemistry.

Discovery of Novel, Orally Bioavailable β-Amino Acid Azaindole Inhibitors of Influenza PB2.

P. Charifson, Alice Tsai, Tiansheng Wang, 2017, ACS medicinal chemistry letters.

Novel 2-Substituted 7-Azaindole and 7-Azaindazole Analogues as Potential Antiviral Agents for the Treatment of Influenza.

F. Maltais, P. Charifson, Alice Tsai, 2017, ACS medicinal chemistry letters.

Total Synthesis of (±)‐Eusiderin G and (±)‐Eusiderin M

W. Gu, Xinfeng Ren, Xin-fu Pan, 2001 .

A NEW APPROACH FOR SYNTHESIS OF ERYTHRO 8-O-4′ NEOLIGNANS

Xiaochuan Chen, W. Gu, Xin-fu Pan, 2002 .

Carbonyl- and sulfur-containing analogs of suberoylanilide hydroxamic acid: Potent inhibition of histone deacetylases.

C. Horvath, R. Silverman, W. Gu, 2006, Bioorganic & medicinal chemistry.

TOTAL SYNTHESIS OF (±)-EUSIDERIN K AND (±)-EUSIDERIN J

W. Gu, Xinfeng Ren, Xin-fu Pan, 2001 .

Celastrols as Inducers of the Heat Shock Response and Cytoprotection*[boxs]

S. Westerheide, R. Morimoto, J. Bosman, 2004, Journal of Biological Chemistry.

Composition of organic matter‑iron‑phosphorus associations in sediments of algae- and macrophyte-dominated zones in Lake Taihu

J. Liu, YingXun Du, Meilian Chen, 2023, Chemical Geology.

Tubulin binding, protein-bound conformation in solution, and antimitotic cellular profiling of noscapine and its derivatives.

Tiansheng Wang, B. Eustace, Á. Canales, 2012, Journal of medicinal chemistry.

Enantioselective syntheses of (S)- and (R)-8,9-dihydroxydihydromagnolol

X. She, W. Gu, Xin-fu Pan, 1998 .

Solid-phase total synthesis of scytalidamide A.

R. Silverman, W. Gu, 2003, The Journal of organic chemistry.

Solid-phase, Pd-catalyzed silicon-aryl carbon bond formation. Synthesis of sansalvamide A peptide.

R. Silverman, W. Gu, Shouxin Liu S, 2002, Organic letters.

Discovery of a novel, first-in-class, orally bioavailable azaindole inhibitor (VX-787) of influenza PB2.

M. Murcko, F. Maltais, P. Charifson, 2014, Journal of medicinal chemistry.

Design, synthesis and biological evaluation of potent NAD+-dependent DNA ligase inhibitors as potential antibacterial agents. Part 2: 4-amino-pyrido[2,3-d]pyrimidin-5(8H)-ones.

P. Charifson, Tiansheng Wang, E. Perola, 2012, Bioorganic & medicinal chemistry letters.

New stable backbone linker resins for solid-phase peptide synthesis.

R. Silverman, W. Gu, 2003, Organic letters.

Application of design of experiments (DoE) optimization to the one-pot synthesis of 4,6-dihydropteridinones.

Tiansheng Wang, Jeremy Green, W. Gu, 2015, Organic & biomolecular chemistry.

Structural basis of noscapine activation for tubulin binding.

M. Steinmetz, A. Prota, Á. Canales, 2020, Journal of medicinal chemistry.

Novel 2-Substituted 7-Azaindole and 7-Azaindazole Analogues as Potential Antiviral Agents for the Treatment of Influenza.

F. Maltais, P. Charifson, Alice Tsai, 2017, ACS medicinal chemistry letters.

Discovery of a novel, first-in-class, orally bioavailable azaindole inhibitor (VX-787) of influenza PB2.

M. Murcko, F. Maltais, P. Charifson, 2014, Journal of medicinal chemistry.