Wen‐xue Chen

发表

Synthesis and biological evaluation of DAPY-DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

E. De Clercq, C. Pannecouque, D. Daelemans, 2015, Bioorganic & medicinal chemistry.

Pyrimidine sulfonylacetanilides with improved potency against key mutant viruses of HIV-1 by specific targeting of a highly conserved residue.

E. De Clercq, C. Pannecouque, D. Daelemans, 2015, European journal of medicinal chemistry.

Synthesis and biological evaluation of new conformationally restricted S-DABO hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptase

C. Pannecouque, J. Balzarini, E. Clercq, 2014 .

Beshanzoides A–D, unprecedented cycloheptanone-containing polyketides from Penicillium commune P-4-1, an endophytic fungus of the endangered conifer Abies beshanzuensis

Yi Zang, J. Xiong, Jin-Feng Hu, 2021, RSC advances.

Asymmetric synthesis of the HMG-CoA reductase inhibitor atorvastatin calcium: an organocatalytic anhydride desymmetrization and cyanide-free side chain elongation approach.

Fangjun Xiong, Fener Chen, Xiaofei Chen, 2014, The Journal of organic chemistry.

Asymmetric Amination of 3‐(2‐Oxoindolin‐3‐ylidene)butanoates Catalyzed by a Cinchona‐derived Alkaloid

C. Zheng, Fen-Er Chen, Wen‐xue Chen, 2015 .

Synthetic studies on statins. Part 1: a short and cyanide-free synthesis of atorvastatin calcium via an enantioselective aldol strategy

Fangjun Xiong, Fener Chen, Xiaofei Chen, 2013 .

Towards new C6-rigid S-DABO HIV-1 reverse transcriptase inhibitors: synthesis, biological investigation and molecular modeling studies.

E. De Clercq, C. Pannecouque, J. Balzarini, 2013, Bioorganic & Medicinal Chemistry.

A Novel and Practical Synthesis of 2-Amino-5-hydroxypropiophenone

Fen-Er Chen, Yunyan Kuang, Xiaodong Xiong, 2009 .

Forrestiacids E-K: Further [4 + 2]-Type Triterpene-Diterpene Hybrids as Potential ACL Inhibitors from the Vulnerable Conifer Pseudotsuga forrestii.

Yi Zang, J. Xiong, Guang-Lei Ma, 2023, Journal of Natural Products.

Design and synthesis of a new series of cyclopropylamino-linking diarylpyrimidines as HIV non-nucleoside reverse transcriptase inhibitors.

E. De Clercq, C. Pannecouque, J. Balzarini, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Design and synthesis of a new series of modified CH-diarylpyrimidines as drug-resistant HIV non-nucleoside reverse transcriptase inhibitors.

E. De Clercq, C. Pannecouque, J. Balzarini, 2014, European journal of medicinal chemistry.

Structural modifications of CH(OH)-DAPYs as new HIV-1 non-nucleoside reverse transcriptase inhibitors.

Christophe Pannecouque, E. De Clercq, C. Pannecouque, 2014, Bioorganic & medicinal chemistry.

Anti-HIV diarylpyrimidine-quinolone hybrids and their mode of action.

E. De Clercq, C. Pannecouque, D. Daelemans, 2015, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors.

Christophe Pannecouque, E. De Clercq, C. Pannecouque, 2014, Bioorganic & medicinal chemistry.