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Zhengqiang Wang, Ph.D. - Publications

Affiliations: 
2003 Wayne State University, Detroit, MI, United States 
Area:
Higher Order Cycloadditions
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65 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Jagtap AD, Geraghty RJ, Wang Z. Inhibiting HCMV pUL89-C Endonuclease with Metal-Binding Compounds. Journal of Medicinal Chemistry. 66: 13874-13887. PMID 37827528 DOI: 10.1021/acs.jmedchem.3c01280  0.313
2023 Dsouza L, Pant A, Offei S, Priyamvada L, Pope B, Satheshkumar PS, Wang Z, Yang Z. Antiviral activities of two nucleos(t)ide analogs against vaccinia, mpox, and cowpox viruses in primary human fibroblasts. Antiviral Research. 216: 105651. PMID 37270160 DOI: 10.1016/j.antiviral.2023.105651  0.333
2023 Dsouza L, Pant A, Offei S, Priyamvada L, Pope B, Satheshkumar PS, Wang Z, Yang Z. Antiviral activities of two nucleos(t)ide analogs against vaccinia and mpox viruses in primary human fibroblasts. Biorxiv : the Preprint Server For Biology. PMID 36993701 DOI: 10.1101/2023.03.23.533943  0.337
2022 He T, Edwards TC, Majima R, Jung E, Kankanala J, Xie J, Geraghty RJ, Wang Z. Repurposing N-hydroxy thienopyrimidine-2,4-diones (HtPD) as inhibitors of human cytomegalovirus pUL89 endonuclease: Synthesis and biological characterization. Bioorganic Chemistry. 129: 106198. PMID 36265353 DOI: 10.1016/j.bioorg.2022.106198  0.415
2022 Jung E, Majima R, Edwards TC, Soto-Acosta R, Geraghty RJ, Wang Z. 8-Hydroxy-1,6-naphthyridine-7-carboxamides as Inhibitors of Human Cytomegalovirus pUL89 Endonuclease. Chemmedchem. PMID 35879245 DOI: 10.1002/cmdc.202200334  0.343
2021 Senaweera S, Edwards TC, Kankanala J, Wang Y, Sahani RL, Xie J, Geraghty RJ, Wang Z. Discovery of -benzyl hydroxypyridone carboxamides as a novel and potent antiviral chemotype against human cytomegalovirus (HCMV). Acta Pharmaceutica Sinica. B. 12: 1671-1684. PMID 35847513 DOI: 10.1016/j.apsb.2021.08.019  0.317
2021 Sahani RL, Akther T, Cilento ME, Castaner AE, Zhang H, Kirby KA, Xie J, Sarafianos SG, Wang Z. Potency and metabolic stability: a molecular hybrid case in the design of novel PF74-like small molecules targeting HIV-1 capsid protein. Rsc Medicinal Chemistry. 12: 2031-2044. PMID 35028563 DOI: 10.1039/d1md00292a  0.355
2021 McFadden WM, Snyder AA, Kirby KA, Tedbury PR, Raj M, Wang Z, Sarafianos SG. Rotten to the core: antivirals targeting the HIV-1 capsid core. Retrovirology. 18: 41. PMID 34937567 DOI: 10.1186/s12977-021-00583-z  0.395
2021 Wang L, Edwards TC, Sahani RL, Xie J, Aihara H, Geraghty RJ, Wang Z. Metal binding 6-arylthio-3-hydroxypyrimidine-2,4-diones inhibited human cytomegalovirus by targeting the pUL89 endonuclease of the terminase complex. European Journal of Medicinal Chemistry. 222: 113640. PMID 34147908 DOI: 10.1016/j.ejmech.2021.113640  0.343
2021 Sahani RL, Diana-Rivero R, Vernekar SKV, Wang L, Du H, Zhang H, Castaner AE, Casey MC, Kirby KA, Tedbury PR, Xie J, Sarafianos SG, Wang Z. Design, Synthesis and Characterization of HIV-1 CA-Targeting Small Molecules: Conformational Restriction of PF74. Viruses. 13. PMID 33804121 DOI: 10.3390/v13030479  0.676
2021 Wang L, Casey MC, Vernekar SKV, Sahani RL, Kirby KA, Du H, Zhang H, Tedbury PR, Xie J, Sarafianos SG, Wang Z. Novel PF74-like small molecules targeting the HIV-1 capsid protein: Balance of potency and metabolic stability. Acta Pharmaceutica Sinica. B. 11: 810-822. PMID 33777683 DOI: 10.1016/J.Apsb.2020.07.016  0.692
2021 Senaweera S, He T, Cui H, Aihara H, Wang Z. 4-Benzylideneisoquinoline-1,3(,)-diones as tyrosyl DNA phosphodiesterase 2 (TDP2) inhibitors. Medicinal Chemistry Research : An International Journal For Rapid Communications On Design and Mechanisms of Action of Biologically Active Agents. 30: 371-386. PMID 33776385 DOI: 10.1007/s00044-020-02662-w  0.339
2020 Wang L, Casey MC, Vernekar SKV, Sahani RL, Kankanala J, Kirby KA, Du H, Hachiya A, Zhang H, Tedbury PR, Xie J, Sarafianos SG, Wang Z. Novel HIV-1 capsid-targeting small molecules of the PF74 binding site. European Journal of Medicinal Chemistry. 204: 112626. PMID 32814250 DOI: 10.1016/J.Ejmech.2020.112626  0.688
2020 Wang L, Casey MC, Vernekar SKV, Do HT, Sahani RL, Kirby KA, Du H, Hachiya A, Zhang H, Tedbury PR, Xie J, Sarafianos SG, Wang Z. Chemical profiling of HIV-1 capsid-targeting antiviral PF74. European Journal of Medicinal Chemistry. 200: 112427. PMID 32438252 DOI: 10.1016/J.Ejmech.2020.112427  0.676
2020 Vernekar SKV, Sahani RL, Casey MC, Kankanala J, Wang L, Kirby KA, Du H, Zhang H, Tedbury PR, Xie J, Sarafianos SG, Wang Z. Toward Structurally Novel and Metabolically Stable HIV-1 Capsid-Targeting Small Molecules. Viruses. 12. PMID 32316297 DOI: 10.3390/V12040452  0.715
2020 Dang X, Ogbu SC, Zhao J, Nguyen LNT, Cao D, Nguyen LN, Khanal S, Schank M, Thakuri BKC, Wu XY, Morrison ZD, Zhang J, Li Z, El Gazzar M, Ning S, ... ... Wang Z, et al. Inhibition of topoisomerase IIA (Top2α) induces telomeric DNA damage and T cell dysfunction during chronic viral infection. Cell Death & Disease. 11: 196. PMID 32193368 DOI: 10.1038/S41419-020-2395-2  0.327
2019 Wang L, Sarafianos SG, Wang Z. Cutting into the Substrate Dominance: Pharmacophore and Structure-Based Approaches toward Inhibiting Human Immunodeficiency Virus Reverse Transcriptase-Associated Ribonuclease H. Accounts of Chemical Research. PMID 31880912 DOI: 10.1021/Acs.Accounts.9B00450  0.55
2019 Kiselev E, Ravji A, Kankanala J, Xie J, Wang Z, Pommier Y. Novel deazaflavin tyrosyl-DNA phosphodiesterase 2 (TDP2) inhibitors. Dna Repair. 85: 102747. PMID 31775111 DOI: 10.1016/J.Dnarep.2019.102747  0.446
2019 Xi Z, Wang Z, Sarafianos SG, Myshakina NS, Ishima R. Determinants of Active-Site Inhibitor Interaction with HIV-1 RNase H. Acs Infectious Diseases. PMID 31577424 DOI: 10.1021/Acsinfecdis.9B00300  0.45
2019 Kankanala J, Ribeiro CJA, Kiselev E, Ravji A, Williams J, Xie J, Aihara H, Pommier Y, Wang Z. Novel deazaflavin analogues potently inhibited tyrosyl DNA phosphodiesterase 2 (TDP2) and strongly sensitized cancer cells toward treatment with topoisomerase II (TOP2) poison etoposide. Journal of Medicinal Chemistry. PMID 30998359 DOI: 10.1021/Acs.Jmedchem.9B00274  0.376
2019 Tang J, Do HT, Huber AD, Casey MC, Kirby KA, Wilson DJ, Kankanala J, Parniak MA, Sarafianos SG, Wang Z. Pharmacophore-based design of novel 3-hydroxypyrimidine-2,4-dione subtypes as inhibitors of HIV reverse transcriptase-associated RNase H: Tolerance of a nonflexible linker. European Journal of Medicinal Chemistry. 166: 390-399. PMID 30739822 DOI: 10.1016/J.Ejmech.2019.01.081  0.578
2018 Tang J, Huber AD, Pineda DL, Boschert KN, Wolf JJ, Kankanala J, Xie J, Sarafianos SG, Wang Z. 5-Aminothiophene-2,4-dicarboxamide analogues as hepatitis B virus capsid assembly effectors. European Journal of Medicinal Chemistry. 164: 179-192. PMID 30594676 DOI: 10.1016/J.Ejmech.2018.12.047  0.371
2018 Huber AD, Pineda DL, Liu D, Boschert KN, Gres AT, Wolf JJ, Coonrod EM, Tang J, Laughlin TG, Yang Q, Puray-Chavez M, Ji J, Singh K, Kirby KA, Wang Z, et al. Novel Hepatitis B Virus Capsid-Targeting Antiviral that Aggregates Core Particles and Inhibits Nuclear Entry of Viral Cores. Acs Infectious Diseases. PMID 30582687 DOI: 10.1021/Acsinfecdis.8B00235  0.377
2018 Ribeiro CJA, Kankanala J, Xie J, Williams J, Aihara H, Wang Z. Triazolopyrimidine and triazolopyridine scaffolds as TDP2 inhibitors. Bioorganic & Medicinal Chemistry Letters. PMID 30522956 DOI: 10.1016/J.Bmcl.2018.11.044  0.372
2018 Wang L, Tang J, Huber AD, Casey MC, Kirby KA, Wilson DJ, Kankanala J, Parniak MA, Sarafianos SG, Wang Z. 6-Biphenylmethyl-3-hydroxypyrimidine-2,4-diones potently and selectively inhibited HIV reverse transcriptase-associated RNase H. European Journal of Medicinal Chemistry. 156: 680-691. PMID 30031978 DOI: 10.1016/J.Ejmech.2018.07.035  0.542
2018 Wang L, Tang J, Huber AD, Casey MC, Kirby KA, Wilson DJ, Kankanala J, Xie J, Parniak MA, Sarafianos SG, Wang Z. 6-Arylthio-3-hydroxypyrimidine-2,4-diones potently inhibited HIV reverse transcriptase-associated RNase H with antiviral activity. European Journal of Medicinal Chemistry. 156: 652-665. PMID 30031976 DOI: 10.1016/J.Ejmech.2018.07.039  0.549
2018 Kankanala J, Wang Y, Geraghty RJ, Wang Z. Hydroxypyridonecarboxylic acids as inhibitors of human cytomegalovirus pUL89 endonuclease. Chemmedchem. PMID 29968426 DOI: 10.1002/Cmdc.201800283  0.441
2018 Bohl TE, Ieong P, Lee JK, Lee T, Kankanala J, Shi K, Demir Ö, Kurahashi K, Amaro RE, Wang Z, Aihara H. The substrate-binding cap of the UDP-diacylglucosamine pyrophosphatase LpxH is highly flexible, enabling facile substrate binding and product release. The Journal of Biological Chemistry. PMID 29626094 DOI: 10.1074/Jbc.Ra118.002503  0.339
2018 Ribeiro CJA, Kankanala J, Shi K, Kurahashi K, Kiselev E, Ravji A, Pommier Y, Aihara H, Wang Z. New fluorescence-based high-throughput screening assay for small molecule inhibitors of tyrosyl-DNA phosphodiesterase 2 (TDP2). European Journal of Pharmaceutical Sciences : Official Journal of the European Federation For Pharmaceutical Sciences. PMID 29574079 DOI: 10.1016/J.Ejps.2018.03.021  0.396
2018 Wang Y, Tang J, Wang Z, Geraghty RJ. Metal-chelating 3-hydroxypyrimidine-2,4-diones inhibit human cytomegalovirus pUL89 endonuclease activity and virus replication. Antiviral Research. PMID 29425830 DOI: 10.1016/J.Antiviral.2018.01.015  0.472
2017 Kankanala J, Kirby KA, Huber AD, Casey MC, Wilson DJ, Sarafianos SG, Wang Z. Design, synthesis and biological evaluations of N-Hydroxy thienopyrimidine-2,4-diones as inhibitors of HIV reverse transcriptase-associated RNase H. European Journal of Medicinal Chemistry. 141: 149-161. PMID 29031062 DOI: 10.1016/J.Ejmech.2017.09.054  0.549
2017 Kirby KA, Myshakina NA, Christen MT, Chen YL, Schmidt HA, Huber AD, Xi Z, Kim S, Rao RK, Kramer ST, Yang Q, Singh K, Parniak MA, Wang Z, Ishima R, et al. A 2-hydroxyisoquinoline-1,3-dione active site RNase H inhibitor binds in multiple modes to HIV-1 reverse transcriptase. Antimicrobial Agents and Chemotherapy. PMID 28760905 DOI: 10.1128/Aac.01351-17  0.66
2017 Vernekar SKV, Tang J, Wu B, Huber AD, Casey MC, Myshakina NS, Wilson DJ, Kankanala J, Kirby KA, Parniak MA, Sarafianos SG, Wang Z. Double-winged 3-Hydroxypyrimidine-2,4-diones: Potent and Selective Inhibition against HIV-1 RNase H with Significant Antiviral Activity. Journal of Medicinal Chemistry. PMID 28525279 DOI: 10.1021/Acs.Jmedchem.7B00440  0.725
2017 Tang J, Vernekar SK, Chen YL, Miller L, Huber AD, Myshakina N, Sarafianos SG, Parniak MA, Wang Z. Synthesis, biological evaluation and molecular modeling of 2-Hydroxyisoquinoline-1,3-dione analogues as inhibitors of HIV reverse transcriptase associated ribonuclease H and polymerase. European Journal of Medicinal Chemistry. 133: 85-96. PMID 28384548 DOI: 10.1016/J.Ejmech.2017.03.059  0.775
2017 Huber AD, Michailidis E, Tang J, Puray-Chavez MN, Boftsi M, Wolf JJ, Boschert KN, Sheridan MA, Leslie MD, Kirby KA, Singh K, Mitsuya H, Parniak MA, Wang Z, Sarafianos SG. 3-hydroxypyrimidine-2,4-diones as novel hepatitis B virus antivirals targeting the viral ribonuclease H. Antimicrobial Agents and Chemotherapy. PMID 28320718 DOI: 10.1128/Aac.00245-17  0.379
2017 Tang J, Kirby KA, Huber AD, Casey MC, Ji J, Wilson DJ, Sarafianos SG, Wang Z. 6-Cyclohexylmethyl-3-hydroxypyrimidine-2,4-dione as an inhibitor scaffold of HIV reverase transcriptase: Impacts of the 3-OH on inhibiting RNase H and polymerase. European Journal of Medicinal Chemistry. 128: 168-179. PMID 28182989 DOI: 10.1016/J.Ejmech.2017.01.041  0.549
2016 Wang Y, Mao L, Kankanala J, Wang Z, Geraghty RJ. Inhibition of Human Cytomegalovirus pUL89 Terminase Subunit Blocks Virus Replication and Genome Cleavage. Journal of Virology. PMID 27881652 DOI: 10.1128/Jvi.02152-16  0.429
2016 Wu B, Tang J, Wilson DJ, Huber AD, Casey MC, Ji J, Kankanala J, Xie J, Sarafianos SG, Wang Z. 3-Hydroxypyrimidine-2,4-dione-5-N-benzylcarboxamides potently inhibit HIV-1 integrase and RNase H. Journal of Medicinal Chemistry. PMID 27283261 DOI: 10.1021/Acs.Jmedchem.6B00040  0.558
2016 Marchand C, Abdelmalak M, Kankanala J, Huang SY, Kiselev E, Fesen K, Kurahashi K, Sasanuma H, Takeda S, Aihara H, Wang Z, Pommier Y. Deazaflavin inhibitors of tyrosyl-DNA phosphodiesterase 2 (TDP2) specific for the human enzyme and active against cellular TDP2. Acs Chemical Biology. PMID 27128689 DOI: 10.1021/Acschembio.5B01047  0.403
2016 Kankanala J, Kirby KA, Liu F, Miller LG, Nagy E, Wilson DJ, Parniak MA, Sarafianos SG, Wang Z. Design, Synthesis and Biological Evaluations of Hydroxypyridone Carboxylic Acids as Inhibitors of HIV Reverse Transcriptase-Associated RNase H. Journal of Medicinal Chemistry. PMID 27094954 DOI: 10.1021/Acs.Jmedchem.6B00465  0.54
2016 Tang J, Liu F, Nagy E, Miller LG, Kirby KA, Wilson DJ, Wu B, Sarafianos SG, Parniak MA, Wang Z. 2-Hydroxypyrimidine-2,4-diones as Selective Active Site Inhibitors of HIV Reverse Transcriptase-Associated RNase H: Design, Synthesis, and Biochemical Evaluations. Journal of Medicinal Chemistry. PMID 26927866 DOI: 10.1021/Acs.Jmedchem.5B01879  0.538
2016 Kankanala J, Marchand C, Abdelmalak M, Aihara H, Pommier Y, Wang Z. Isoquinoline-1,3-diones as Selective Inhibitors of Tyrosyl DNA Phosphodiesterase II (TDP2). Journal of Medicinal Chemistry. PMID 26910725 DOI: 10.1021/Acs.Jmedchem.5B01973  0.403
2016 Chen Y, Chen L, Ou Y, Wang Z, Fu F, Guo L. DNAzyme-based biosensor for Cu2+ ion by combining hybridization chain reaction with fluorescence resonance energy transfer technique Talanta. 155: 245-249. DOI: 10.1016/j.talanta.2016.04.057  0.431
2016 He B, Wang ZJ, Chen YN, Zhang ZD. Enhanced magnetic and ferroelectric properties in Pb(Zr0.52Ti0.48)O3/La0.7Ca0.3MnO3 bilayers grown on Nb-doped (110) SrTiO3 substrate Journal of Alloys and Compounds. 680: 565-570. DOI: 10.1016/j.jallcom.2016.04.177  0.414
2016 Gang C, Wang Z, Chen Y, Yang Y, Li J, Cheng J, Qi J, Odeh I. Drought-induced dynamics of carbon and water use efficiency of global grasslands from 2000 to 2011 Ecological Indicators. 67: 788-797. DOI: 10.1016/J.Ecolind.2016.03.049  0.433
2016 Wang Z, Chen Y, Xie P, Shang R, Ma J. Removal of Microcystis aeruginosa by UV-activated persulfate: Performance and characteristics Chemical Engineering Journal. 300: 245-253. DOI: 10.1016/j.cej.2016.04.125  0.451
2015 Vernekar SK, Qiu L, Zhang J, Kankanala J, Li H, Geraghty RJ, Wang Z. 5'-Silylated 3'-1,2,3-triazolyl Thymidine Analogues as Inhibitors of West Nile Virus and Dengue Virus. Journal of Medicinal Chemistry. 58: 4016-28. PMID 25909386 DOI: 10.1021/Acs.Jmedchem.5B00327  0.708
2015 Vernekar SK, Liu Z, Nagy E, Miller L, Kirby KA, Wilson DJ, Kankanala J, Sarafianos SG, Parniak MA, Wang Z. Design, synthesis, biochemical, and antiviral evaluations of C6 benzyl and C6 biarylmethyl substituted 2-hydroxylisoquinoline-1,3-diones: dual inhibition against HIV reverse transcriptase-associated RNase H and polymerase with antiviral activities. Journal of Medicinal Chemistry. 58: 651-64. PMID 25522204 DOI: 10.1021/Jm501132S  0.723
2014 Vernekar SKV, Qiu L, Zacharias J, Geraghty RJ, Wang Z. Synthesis and antiviral evaluation of 4′-(1,2,3-triazol-1-yl) thymidines Medchemcomm. 5: 603-608. DOI: 10.1039/C4Md00039K  0.732
2013 Sirivolu VR, Vernekar SK, Ilina T, Myshakina NS, Parniak MA, Wang Z. Clicking 3'-azidothymidine into novel potent inhibitors of human immunodeficiency virus. Journal of Medicinal Chemistry. 56: 8765-80. PMID 24102161 DOI: 10.1021/Jm401232V  0.795
2012 Sirivolu VR, Vernekar SK, Marchand C, Naumova A, Chergui A, Renaud A, Stephen AG, Chen F, Sham YY, Pommier Y, Wang Z. 5-Arylidenethioxothiazolidinones as inhibitors of tyrosyl-DNA phosphodiesterase I. Journal of Medicinal Chemistry. 55: 8671-84. PMID 23006064 DOI: 10.1021/Jm3008773  0.769
2012 Chen YL, Zacharias J, Vince R, Geraghty RJ, Wang Z. C-6 aryl substituted 4-quinolone-3-carboxylic acids as inhibitors of hepatitis C virus. Bioorganic & Medicinal Chemistry. 20: 4790-800. PMID 22748708 DOI: 10.1016/J.Bmc.2012.05.066  0.762
2012 Kirby KA, Marchand B, Ong YT, Ndongwe TP, Hachiya A, Michailidis E, Leslie MD, Sietsema DV, Fetterly TL, Dorst CA, Singh K, Wang Z, Parniak MA, Sarafianos SG. Structural and inhibition studies of the RNase H function of xenotropic murine leukemia virus-related virus reverse transcriptase. Antimicrobial Agents and Chemotherapy. 56: 2048-61. PMID 22252812 DOI: 10.1128/Aac.06000-11  0.501
2012 Chen YL, Tang J, Kesler MJ, Sham YY, Vince R, Geraghty RJ, Wang Z. The design, synthesis and biological evaluations of C-6 or C-7 substituted 2-hydroxyisoquinoline-1,3-diones as inhibitors of hepatitis C virus. Bioorganic & Medicinal Chemistry. 20: 467-79. PMID 22100256 DOI: 10.1016/J.Bmc.2011.10.058  0.762
2011 Tang J, Maddali K, Dreis CD, Sham YY, Vince R, Pommier Y, Wang Z. N-3 Hydroxylation of Pyrimidine-2,4-diones Yields Dual Inhibitors of HIV Reverse Transcriptase and Integrase. Acs Medicinal Chemistry Letters. 2: 63-67. PMID 21499541 DOI: 10.1021/Ml1002162  0.751
2011 Tang J, Maddali K, Dreis CD, Sham YY, Vince R, Pommier Y, Wang Z. 6-Benzoyl-3-hydroxypyrimidine-2,4-diones as dual inhibitors of HIV reverse transcriptase and integrase. Bioorganic & Medicinal Chemistry Letters. 21: 2400-2. PMID 21392991 DOI: 10.1016/J.Bmcl.2011.02.069  0.765
2011 Tang J, Maddali K, Metifiot M, Sham YY, Vince R, Pommier Y, Wang Z. 3-Hydroxypyrimidine-2,4-diones as an inhibitor scaffold of HIV integrase. Journal of Medicinal Chemistry. 54: 2282-92. PMID 21381765 DOI: 10.1021/Jm1014378  0.764
2010 Wang Z, Tang J, Salomon CE, Dreis CD, Vince R. Pharmacophore and structure-activity relationships of integrase inhibition within a dual inhibitor scaffold of HIV reverse transcriptase and integrase. Bioorganic & Medicinal Chemistry. 18: 4202-11. PMID 20576573 DOI: 10.1016/J.Bmc.2010.05.004  0.774
2010 Tang J, Maddali K, Pommier Y, Sham YY, Wang Z. Scaffold rearrangement of dihydroxypyrimidine inhibitors of HIV integrase: Docking model revisited. Bioorganic & Medicinal Chemistry Letters. 20: 3275-9. PMID 20457521 DOI: 10.1016/J.Bmcl.2010.04.048  0.517
2008 Wang Z, Vince R. Design and synthesis of dual inhibitors of HIV reverse transcriptase and integrase: introducing a diketoacid functionality into delavirdine. Bioorganic & Medicinal Chemistry. 16: 3587-95. PMID 18314335 DOI: 10.1016/J.Bmc.2008.02.007  0.758
2008 Wang Z, Vince R. Synthesis of pyrimidine and quinolone conjugates as a scaffold for dual inhibitors of HIV reverse transcriptase and integrase. Bioorganic & Medicinal Chemistry Letters. 18: 1293-6. PMID 18226894 DOI: 10.1016/J.Bmcl.2008.01.025  0.75
2008 WANG Z, VINCE R. From RT Inhibitor to RT/IN Dual Inhibitor: An Rational Design Antiviral Research. 78: A51-A51. DOI: 10.1016/J.Antiviral.2008.01.103  0.689
2007 Wang Z, Bennett EM, Wilson DJ, Salomon C, Vince R. Rationally designed dual inhibitors of HIV reverse transcriptase and integrase. Journal of Medicinal Chemistry. 50: 3416-9. PMID 17608468 DOI: 10.1021/Jm070512P  0.747
2003 Rigby JH, Wang Z. Synthesis of highly substituted cyclopentenones via the [4 + 1] cycloaddition of nucleophilic carbenes and vinyl ketenes. Organic Letters. 5: 263-4. PMID 12556167 DOI: 10.1021/Ol0272141  0.538
2002 Rigby JH, Wang Z. [4 + 1] cycloaddition of N-heterocyclic carbenes with vinyl isocyanates. Organic Letters. 4: 4289-91. PMID 12443080 DOI: 10.1021/Ol026927G  0.515
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