| Year |
Citation |
Score |
| 2023 |
Nie X, Zhao Y, Tang H, Zhang Z, Liao J, Almodovar-Rivera CM, Sundaresan R, Xie H, Guo L, Wang B, Guan H, Xing Y, Tang W. Development of Phenyl-substituted Isoindolinone- and Benzimidazole-Type Cereblon Ligands for Targeted Protein Degradation. Chembiochem : a European Journal of Chemical Biology. e202300685. PMID 38116854 DOI: 10.1002/cbic.202300685 |
0.594 |
|
| 2023 |
Xie H, Bacabac MS, Ma M, Kim EJ, Wang Y, Wu W, Li L, Xu W, Tang W. Development of Potent and Selective Coactivator-Associated Arginine Methyltransferase 1 (CARM1) Degraders. Journal of Medicinal Chemistry. PMID 37703322 DOI: 10.1021/acs.jmedchem.3c00982 |
0.604 |
|
| 2023 |
Wu J, Jia P, Kuniyil R, Liu P, Tang W. Dynamic Kinetic Stereoselective Glycosylation via Rh and Chiral Phosphoric Acid-Cocatalyzed Carbenoid Insertion to the Anomeric OH Bond for the Synthesis of Glycoconjugates. Angewandte Chemie (International Ed. in English). e202307144. PMID 37532672 DOI: 10.1002/anie.202307144 |
0.333 |
|
| 2023 |
Almodóvar-Rivera CM, Zhang Z, Li J, Xie H, Zhao Y, Guo L, Mannhardt MG, Tang W. A Modular Chemistry Platform for the Development of a Cereblon E3 Ligase-based Partial PROTAC Library. Chembiochem : a European Journal of Chemical Biology. e202300482. PMID 37418320 DOI: 10.1002/cbic.202300482 |
0.601 |
|
| 2023 |
Li J, Li C, Zhang Z, Zhang Z, Wu Z, Liao J, Wang Z, McReynolds M, Xie H, Guo L, Fan Q, Peng J, Tang W. A platform for the rapid synthesis of molecular glues (Rapid-Glue) under miniaturized conditions for direct biological screening. European Journal of Medicinal Chemistry. 258: 115567. PMID 37390512 DOI: 10.1016/j.ejmech.2023.115567 |
0.61 |
|
| 2023 |
Stevens CM, Zhou Y, Teng P, Rault LN, Liao Y, Tang W. Development of Oligomeric Mannose-6-phosphonate Conjugates for Targeted Protein Degradation. Acs Medicinal Chemistry Letters. 14: 719-726. PMID 37312839 DOI: 10.1021/acsmedchemlett.2c00479 |
0.546 |
|
| 2023 |
Xie H, Li C, Tang H, Tandon I, Liao J, Roberts BL, Zhao Y, Tang W. Development of Substituted Phenyl Dihydrouracil as the Novel Achiral Cereblon Ligands for Targeted Protein Degradation. Journal of Medicinal Chemistry. PMID 36749666 DOI: 10.1021/acs.jmedchem.2c01941 |
0.58 |
|
| 2022 |
Donahue K, Xie H, Li M, Gao A, Ma M, Wang Y, Tipton R, Semanik N, Primeau T, Li S, Li L, Tang W, Xu W. Diptoindonesin G is a middle domain HSP90 modulator for cancer treatment. The Journal of Biological Chemistry. 102700. PMID 36395883 DOI: 10.1016/j.jbc.2022.102700 |
0.512 |
|
| 2022 |
Li X, Wu J, Tang W. General Strategy for the Synthesis of Rare Sugars via Ru(II)-Catalyzed and Boron-Mediated Selective Epimerization of 1,2--Diols to 1,2--Diols. Journal of the American Chemical Society. PMID 35168319 DOI: 10.1021/jacs.1c13399 |
0.329 |
|
| 2021 |
Wen P, Jia P, Fan Q, McCarty BJ, Tang W. Streamlined Iterative Assembly of Thio-oligosaccharides by Aqueous S-Glycosylation of Diverse Deoxythio Sugars. Chemsuschem. PMID 34911160 DOI: 10.1002/cssc.202102483 |
0.302 |
|
| 2021 |
Wang B, Liu J, Tandon I, Wu S, Teng P, Liao J, Tang W. Development of MDM2 degraders based on ligands derived from Ugi reactions: Lessons and discoveries. European Journal of Medicinal Chemistry. 219: 113425. PMID 33862513 DOI: 10.1016/j.ejmech.2021.113425 |
0.6 |
|
| 2021 |
Zhou Y, Teng P, Montgomery NT, Li X, Tang W. Development of Triantennary N-Acetylgalactosamine Conjugates as Degraders for Extracellular Proteins. Acs Central Science. 7: 499-506. PMID 33791431 DOI: 10.1021/acscentsci.1c00146 |
0.534 |
|
| 2020 |
Xie H, Yang K, Winston-McPherson GN, Stapleton DS, Keller MP, Attie AD, Smith KA, Tang W. From methylene bridged diindole to carbonyl linked benzimidazoleindole: Development of potent and metabolically stable PCSK9 modulators. European Journal of Medicinal Chemistry. 206: 112678. PMID 32823006 DOI: 10.1016/J.Ejmech.2020.112678 |
0.6 |
|
| 2020 |
Wang J, Blaszczyk SA, Li X, Tang W. Transition Metal-Catalyzed Selective Carbon-Carbon Bond Cleavage of Vinylcyclopropanes in Cycloaddition Reactions. Chemical Reviews. PMID 32786421 DOI: 10.1021/Acs.Chemrev.0C00160 |
0.311 |
|
| 2020 |
Ye W, Stevens CM, Wen P, Simmons CJ, Tang W. Mild Cu(OTf)2-mediated C-glycosylation with Chelation-Assisted Picolinate as a Leaving Group. The Journal of Organic Chemistry. PMID 32691596 DOI: 10.1021/Acs.Joc.0C01041 |
0.314 |
|
| 2020 |
Yang K, Zhao Y, Nie X, Wu H, Wang B, Almodovar-Rivera CM, Xie H, Tang W. A Cell-Based Target Engagement Assay for the Identification of Cereblon E3 Ubiquitin Ligase Ligands and Their Application in HDAC6 Degraders. Cell Chemical Biology. PMID 32413286 DOI: 10.1016/J.Chembiol.2020.04.008 |
0.606 |
|
| 2020 |
Yang K, Wu H, Zhang Z, Leisten ED, Nie X, Liu B, Wen Z, Zhang J, Cunningham MD, Tang W. Development of Selective Histone Deacetylase 6 (HDAC6) Degraders Recruiting Von Hippel-Lindau (VHL) E3 Ubiquitin Ligase. Acs Medicinal Chemistry Letters. 11: 575-581. PMID 32292566 DOI: 10.1021/Acsmedchemlett.0C00046 |
0.377 |
|
| 2020 |
Roberts BL, Ma ZX, Gao A, Leisten ED, Yin D, Xu W, Tang W. Two-stage Strategy for Development of Proteolysis Targeting Chimeras and its Application for Estrogen Receptor Degraders. Acs Chemical Biology. PMID 32255606 DOI: 10.1021/Acschembio.0C00140 |
0.367 |
|
| 2020 |
Liu J, Ye W, Wang S, Zheng J, Tang W, Li X. Synthesis of Lactams via Ir-Catalyzed C-H Amidation Involving Ir-nitrene Intermediates. The Journal of Organic Chemistry. PMID 32103669 DOI: 10.1021/Acs.Joc.0C00157 |
0.423 |
|
| 2020 |
Wen P, Simmons CJ, Ma ZX, Blaszczyk SA, Balzer PG, Ye W, Duan X, Wang HY, Yin D, Stevens CM, Tang W. Synthesis of Glycosyl Chlorides and Bromides by Chelation Assisted Activation of Picolinic Esters under Mild Neutral Conditions. Organic Letters. PMID 32026682 DOI: 10.1021/Acs.Orglett.0C00078 |
0.628 |
|
| 2020 |
Wu H, Liu B, Yang K, Winston-McPherson GN, Leisten ED, Vezina CM, Ricke WA, Peterson RE, Tang W. Synthesis and biological evaluation of FICZ analogues as agonists of aryl hydrocarbon receptor. Bioorganic & Medicinal Chemistry Letters. 126959. PMID 31952965 DOI: 10.1016/J.Bmcl.2020.126959 |
0.36 |
|
| 2020 |
Luo N, Liao J, Ouyang L, Wen H, Zhong Y, Liu J, Tang W, Luo R. Highly Selective Hydroxylation and Alkoxylation of Silanes: One-Pot Silane Oxidation and Reduction of Aldehydes/Ketones Organometallics. 39: 165-171. DOI: 10.1021/Acs.Organomet.9B00716 |
0.36 |
|
| 2020 |
Liu J, Ye W, Wang S, Zheng J, Tang W, Li X. Synthesis of Lactamsvia Ir-Catalyzed C–H AmidationInvolving Ir-Nitrene Intermediates Journal of Organic Chemistry. DOI: 10.1021/Acs.Joc.0C00157.S001 |
0.429 |
|
| 2019 |
Klein MA, Liu C, Kuznetsov VI, Feltenberger JB, Tang W, Denu JM. Mechanism of activation for the sirtuin 6 protein deacylase. The Journal of Biological Chemistry. PMID 31822559 DOI: 10.1074/Jbc.Ra119.011285 |
0.316 |
|
| 2019 |
Blaszczyk SA, Glazier DA, Tang W. Rhodium-Catalyzed (5 + 2) and (5 + 1) Cycloadditions Using 1,4-Enynes as Five-Carbon Building Blocks. Accounts of Chemical Research. PMID 31820914 DOI: 10.1021/Acs.Accounts.9B00477 |
0.48 |
|
| 2019 |
Wu J, Li X, Qi X, Duan X, Cracraft WL, Guzei IA, Liu P, Tang W. Site- and Stereoselective O-Alkylation of Glycosides by Rh(II)-Catalyzed Carbenoid Insertion. Journal of the American Chemical Society. PMID 31739665 DOI: 10.1021/Jacs.9B11262 |
0.405 |
|
| 2019 |
Zhao C, Ye Z, Ma ZX, Wildman SA, Blaszczyk SA, Hu L, Guizei IA, Tang W. A general strategy for diversifying complex natural products to polycyclic scaffolds with medium-sized rings. Nature Communications. 10: 4015. PMID 31488839 DOI: 10.1038/S41467-019-11976-2 |
0.39 |
|
| 2019 |
Wu H, Yang K, Zhang Z, Leisten E, Li Z, Xie H, Liu J, Smith KA, Novakova Z, Barinka C, Tang W. Development of Multi-Functional Histone Deacetylase 6 Degraders with Potent Anti-Myeloma Activity. Journal of Medicinal Chemistry. PMID 31271281 DOI: 10.1021/Acs.Jmedchem.9B00516 |
0.63 |
|
| 2019 |
Winston-McPherson GN, Xie H, Yang K, Li X, Shu D, Tang W. Discovery of 2,3'-diindolylmethanes as a novel class of PCSK9 modulators. Bioorganic & Medicinal Chemistry Letters. PMID 31227343 DOI: 10.1016/J.Bmcl.2019.06.014 |
0.594 |
|
| 2019 |
Wang B, Wu S, Liu J, Yang K, Xie H, Tang W. Development of selective small molecule MDM2 degraders based on nutlin. European Journal of Medicinal Chemistry. 176: 476-491. PMID 31128449 DOI: 10.1016/J.Ejmech.2019.05.046 |
0.6 |
|
| 2019 |
Blaszczyk SA, Xiao G, Wen P, Hao H, Wu J, Wang B, Carattino F, Li Z, Glazier DA, McCarty BJ, Liu P, Tang W. S-Adamantyl Group Directed Site-Selective Acylation and Its Applications in the Streamlined Assembly of Oligosaccharides. Angewandte Chemie (International Ed. in English). PMID 31066162 DOI: 10.1002/Anie.201903587 |
0.614 |
|
| 2019 |
Blaszczyk SA, Homan TC, Tang W. Recent advances in site-selective functionalization of carbohydrates mediated by organocatalysts. Carbohydrate Research. 471: 64-77. PMID 30508658 DOI: 10.1016/J.Carres.2018.11.012 |
0.384 |
|
| 2019 |
Li J, Tang W, Ren D, Xu J, Yang Z. Iridium-catalysed highly selective reduction–elimination of steroidal 4-en-3-ones to 3,5-dienes in water Green Chemistry. 21: 2088-2094. DOI: 10.1039/C9Gc00654K |
0.406 |
|
| 2019 |
Luo N, Liao J, Ouyang L, Wen H, Liu J, Tang W, Luo R. Highly pH-Dependent Chemoselective Transfer Hydrogenation of α,β-Unsaturated Aldehydes in Water Organometallics. 38: 3025-3031. DOI: 10.1021/Acs.Organomet.9B00353 |
0.301 |
|
| 2019 |
Glazier DA, Schroeder JM, Blaszczyk SA, Tang W. Site‐ and Stereoselective Phosphoramidation of Carbohydrates Using a Chiral Catalyst and a Chiral Electrophile Advanced Synthesis & Catalysis. 361: 3729-3732. DOI: 10.1002/Adsc.201900382 |
0.35 |
|
| 2018 |
Zhao C, Glazier DA, Yang D, Yin D, Guzei IA, Aristov MM, Liu P, Tang W. Intermolecular Regio- and Stereoselective Hetero-[5+2] Cycloaddition between Oxidopyrylium Ylide and Cyclic Imine: Facile Access to Highly Substituted Azepanes. Angewandte Chemie (International Ed. in English). PMID 30476368 DOI: 10.1002/Anie.201811896 |
0.429 |
|
| 2018 |
Yang K, Song Y, Xie H, Wu H, Wu YT, Leisten ED, Tang W. Development of the first small molecule histone deacetylase 6 (HDAC6) degraders. Bioorganic & Medicinal Chemistry Letters. PMID 29871848 DOI: 10.1016/J.Bmcl.2018.05.057 |
0.607 |
|
| 2018 |
Liu J, Yang S, Tang W, Yang Z, Xu J. Iridium-catalyzed efficient reduction of ketones in water with formic acid as a hydride donor at low catalyst loading Green Chemistry. 20: 2118-2124. DOI: 10.1039/C8Gc00348C |
0.371 |
|
| 2018 |
Yang S, Tang W, Yang Z, Xu J. Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols Acs Catalysis. 8: 9320-9326. DOI: 10.1021/Acscatal.8B02495 |
0.404 |
|
| 2018 |
Zhu Z, Glazier DA, Yang D, Tang W. Catalytic Asymmetric Synthesis of All Possible Stereoisomers of 2,3,4,6‐Tetradeoxy‐4‐Aminohexopyranosides Advanced Synthesis & Catalysis. 360: 2211-2215. DOI: 10.1002/Adsc.201800029 |
0.418 |
|
| 2017 |
Seok SH, Ma ZX, Feltenberger JB, Chen H, Chen H, Scarlett C, Lin Z, Satyshur KA, Cortopassi M, Jefcoate CR, Ge Y, Tang W, Bradfield CA, Xing Y. Trace Derivatives of Kynurenine Potently Activate the Aryl Hydrocarbon Receptor (AHR). The Journal of Biological Chemistry. PMID 29279331 DOI: 10.1074/Jbc.Ra117.000631 |
0.344 |
|
| 2017 |
Wang HY, Blaszczyk SA, Xiao G, Tang W. Chiral reagents in glycosylation and modification of carbohydrates. Chemical Society Reviews. PMID 29206256 DOI: 10.1039/C7Cs00432J |
0.738 |
|
| 2017 |
Wang HY, Simmons CJ, Blaszczyk SA, Balzer PG, Luo R, Duan X, Tang W. Isoquinoline-1-carboxylate as a Traceless Leaving Group for Chelation-Assisted Glycosylation under Mild Neutral Conditions. Angewandte Chemie (International Ed. in English). PMID 29048770 DOI: 10.1002/Anie.201708920 |
0.619 |
|
| 2017 |
Song W, Blaszczyk SA, Liu J, Wang S, Tang W. Transition metal mediated carbonylative benzannulations. Organic & Biomolecular Chemistry. PMID 28875209 DOI: 10.1039/C7Ob01000A |
0.334 |
|
| 2017 |
Song W, Wang S, Tang W. De novo Synthesis of Mono- and Oligosaccharides via Dihydropyran Intermediates. Chemistry, An Asian Journal. PMID 28319359 DOI: 10.1002/Asia.201700212 |
0.39 |
|
| 2017 |
Xiao G, Cintron-Rosado GA, Glazier DA, Xi B, Liu C, Liu P, Tang W. Catalytic Site-selective Acylation of Carbohydrates Directed by Cation-n Interaction. Journal of the American Chemical Society. PMID 28297601 DOI: 10.1021/Jacs.7B01412 |
0.58 |
|
| 2017 |
Wang HY, Simmons CJ, Zhang Y, Smits AM, Balzer PG, Wang S, Tang W. Chiral Catalyst-Directed Dynamic Kinetic Diastereoselective Acylation of Anomeric Hydroxyl Groups and a Controlled Reduction of the Glycosyl Ester Products. Organic Letters. PMID 28080072 DOI: 10.1021/Acs.Orglett.6B03683 |
0.62 |
|
| 2017 |
Jaskula-Sztul R, Chen G, Dammalapati A, Harrison A, Tang W, Gong S, Chen H. AB3-Loaded and Tumor-Targeted Unimolecular Micelles for Medullary Thyroid Cancer Treatment. Journal of Materials Chemistry. B, Materials For Biology and Medicine. 5: 151-159. PMID 28025618 DOI: 10.1039/C6Tb02530G |
0.302 |
|
| 2017 |
Yang Z, Zhu Z, Luo R, Qiu X, Liu J, Yang J, Tang W. Iridium-catalyzed highly efficient chemoselective reduction of aldehydes in water using formic acid as the hydrogen source Green Chemistry. 19: 3296-3301. DOI: 10.1039/C7Gc01289F |
0.327 |
|
| 2017 |
Yang Z, Luo R, Zhu Z, Yang X, Tang W. Harnessing the Reactivity of Iridium Hydrides by Air: Iridium-Catalyzed Oxidation of Aldehydes to Acids in Water Organometallics. 36: 4095-4098. DOI: 10.1021/Acs.Organomet.7B00634 |
0.309 |
|
| 2017 |
Zhu Z, Wang H, Simmons C, Tseng P, Qiu X, Zhang Y, Duan X, Yang J, Tang W. Iridium-Catalyzed Dynamic Kinetic Stereoselective Allylic Etherification of Achmatowicz Rearrangement Products Advanced Synthesis & Catalysis. 360: 595-599. DOI: 10.1002/Adsc.201700950 |
0.602 |
|
| 2017 |
Liu J, Simmons CJ, Xie H, Yang F, Zhao X, Tang Y, Tang W. Synthesis of Highly Substituted Benzofuran–containing Natural Products via Rh–catalyzed Carbonylative Benzannulation Advanced Synthesis & Catalysis. 359: 693-697. DOI: 10.1002/Adsc.201600992 |
0.669 |
|
| 2016 |
Hideshima T, Qi J, Paranal RM, Tang W, Greenberg E, West N, Colling ME, Estiu G, Mazitschek R, Perry JA, Ohguchi H, Cottini F, Mimura N, Görgün G, Tai YT, et al. Discovery of selective small-molecule HDAC6 inhibitor for overcoming proteasome inhibitor resistance in multiple myeloma. Proceedings of the National Academy of Sciences of the United States of America. PMID 27799547 DOI: 10.1073/Pnas.1608067113 |
0.595 |
|
| 2016 |
Liu JT, Do TJ, Simmons CJ, Lynch JC, Gu W, Ma ZX, Xu W, Tang W. Total synthesis of diptoindonesin G and its analogues as selective modulators of estrogen receptors. Organic & Biomolecular Chemistry. 14: 8927-8930. PMID 27714255 DOI: 10.1039/C6Ob01657J |
0.38 |
|
| 2016 |
Song W, Li X, Yang K, Zhao XL, Glazier DA, Xi BM, Tang W. Correction to Synthesis of Carbazoles and Carbazole-Containing Heterocycles via Rhodium-Catalyzed Tandem Carbonylative Benzannulations. The Journal of Organic Chemistry. PMID 27564916 DOI: 10.1021/Acs.Joc.6B01809 |
0.442 |
|
| 2016 |
Li X, Xie H, Fu X, Liu J, Wang HY, Xi BM, Liu P, Xu X, Tang W. Rhodium(I)-Catalyzed Benzannulation of Heteroaryl Propargylic Esters: Synthesis of Indoles and Related Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27189811 DOI: 10.1002/Chem.201602088 |
0.738 |
|
| 2016 |
Li X, Song W, Zhao XL, Ke X, Xu X, Liu P, Houk KN, Tang W. Rhodium-Catalyzed [5+2] Cycloaddition of Inverted 3-Acyloxy-1,4-enyne and Alkyne: Experimental and Theoretical Studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26990319 DOI: 10.1002/Chem.201601195 |
0.374 |
|
| 2016 |
Song W, Li X, Yang K, Zhao XL, Glazier DA, Xi BM, Tang W. Synthesis of Carbazoles and Carbazole-containing Heterocycles via Rhodium-Catalyzed Tandem Carbonylative Benzannulations. The Journal of Organic Chemistry. PMID 26963834 DOI: 10.1021/Acs.Joc.6B00212 |
0.437 |
|
| 2016 |
Liu R, Wang J, Tang W, Fang H. Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors. Bioorganic & Medicinal Chemistry. PMID 26907204 DOI: 10.1016/J.Bmc.2016.02.005 |
0.367 |
|
| 2016 |
Song W, Lynch JC, Shu X, Tang W. Rhodium‐Catalyzed [5+2] Cycloaddition of 3‐Acyloxy‐1,4‐enyne with Alkene or Allene Advanced Synthesis & Catalysis. 358: 2007-2011. DOI: 10.1002/Adsc.201600196 |
0.644 |
|
| 2015 |
Ke XN, Schienebeck CM, Zhou CC, Xu X, Tang W. Mechanism and Reactivity of Rh-Catalyzed Intermolecular [5+1] Cycloaddition of 3-Acyloxy-1,4-Enyne (ACE) and CO: A Computational Study. Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao. 26: 730-734. PMID 27152064 DOI: 10.1016/J.Cclet.2015.03.016 |
0.379 |
|
| 2015 |
Schienebeck CM, Song W, Smits AM, Tang W. Rhodium-Catalyzed Intermolecular [5+1] and [5+2] Cycloadditions Using 1,4-Enynes with an Electron-Donating Ester on the 3-Position. Synthesis. 47: 1076-1084. PMID 26508806 DOI: 10.1055/S-0034-1380160 |
0.334 |
|
| 2015 |
Wang HY, Yang K, Yin D, Liu C, Glazier DA, Tang W. Chiral Catalyst-Directed Dynamic Kinetic Diastereoselective Acylation of Lactols for De Novo Synthesis of Carbohydrate. Organic Letters. PMID 26484422 DOI: 10.1021/Acs.Orglett.5B02641 |
0.655 |
|
| 2015 |
Li X, Li H, Song W, Tseng PS, Liu L, Guzei IA, Tang W. Divergent Reactivity of Rhodium(I) Carbenes Derived from Indole Annulations. Angewandte Chemie (International Ed. in English). 54: 12905-8. PMID 26480329 DOI: 10.1002/Anie.201505329 |
0.352 |
|
| 2015 |
Song W, Zhao Y, Lynch JC, Kim H, Tang W. Divergent de novo synthesis of all eight stereoisomers of 2,3,6-trideoxyhexopyranosides and their oligomers. Chemical Communications (Cambridge, England). PMID 26477956 DOI: 10.1039/C5Cc07787G |
0.371 |
|
| 2015 |
Song W, Xi BM, Yang K, Tang W. Synthesis of Substituted Tropones by Sequential Rh-Catalyzed [5+2] Cycloaddition and Elimination. Tetrahedron. 71: 5979-5984. PMID 26456984 DOI: 10.1016/J.Tet.2015.04.039 |
0.388 |
|
| 2015 |
Shu XZ, Schienebeck CM, Li X, Zhou X, Song W, Chen L, Guzei IA, Tang W. Rhodium-Catalyzed Stereoselective Intramolecular [5 + 2] Cycloaddition of 3-Acyloxy 1,4-Enyne and Alkene. Organic Letters. PMID 26440751 DOI: 10.1021/Acs.Orglett.5B02665 |
0.655 |
|
| 2015 |
Wang L, Hou X, Fu H, Pan X, Xu W, Tang W, Fang H. Design, synthesis and preliminary bioactivity evaluations of substituted quinoline hydroxamic acid derivatives as novel histone deacetylase (HDAC) inhibitors. Bioorganic & Medicinal Chemistry. PMID 26149591 DOI: 10.1016/J.Bmc.2015.06.024 |
0.382 |
|
| 2015 |
Wang HY, Yang K, Bennett SR, Guo SR, Tang W. Iridium-Catalyzed Dynamic Kinetic Isomerization: Expedient Synthesis of Carbohydrates from Achmatowicz Rearrangement Products. Angewandte Chemie (International Ed. in English). PMID 26033736 DOI: 10.1002/Anie.201503151 |
0.651 |
|
| 2015 |
Winston-McPherson GN, Tang W. Gold versus Rhodium: Divergent Reactivity Enabled by the Catalyst Chemcatchem. 7: 574-576. DOI: 10.1002/Cctc.201402915 |
0.306 |
|
| 2014 |
Liu N, Song W, Schienebeck CM, Zhang M, Tang W. Synthesis of Naturally Occurring Tropones and Tropolones. Tetrahedron. 70: 9281-9305. PMID 25400298 DOI: 10.1016/J.Tet.2014.07.065 |
0.409 |
|
| 2014 |
Guan P, Wang L, Hou X, Wan Y, Xu W, Tang W, Fang H. Improved antiproliferative activity of 1,3,4-thiadiazole-containing histone deacetylase (HDAC) inhibitors by introduction of the heteroaromatic surface recognition motif. Bioorganic & Medicinal Chemistry. 22: 5766-75. PMID 25311567 DOI: 10.1016/J.Bmc.2014.09.039 |
0.34 |
|
| 2014 |
Li H, Li X, Wang HY, Winston-McPherson GN, Geng HM, Guzei IA, Tang W. Copper-catalyzed tandem annulation/arylation for the synthesis of diindolylmethanes from propargylic alcohols. Chemical Communications (Cambridge, England). 50: 12293-6. PMID 25178910 DOI: 10.1039/C4Cc05901H |
0.617 |
|
| 2014 |
Winston-McPherson GN, Shu D, Tang W. Synthesis and biological evaluation of 2,3'-diindolylmethanes as agonists of aryl hydrocarbon receptor. Bioorganic & Medicinal Chemistry Letters. 24: 4023-5. PMID 24997686 DOI: 10.1016/J.Bmcl.2014.06.009 |
0.369 |
|
| 2014 |
Schienebeck CM, Li X, Shu XZ, Tang W. 3-Acyloxy-1,4-enyne: a New Five-carbon Synthon for Rhodium-Catalyzed (5+2) Cycloadditions. Pure and Applied Chemistry. Chimie Pure Et Appliquee. 86: 409-417. PMID 24839310 DOI: 10.1515/Pac-2014-5042 |
0.654 |
|
| 2014 |
Han L, Wang L, Hou X, Fu H, Song W, Tang W, Fang H. Design, synthesis and preliminary bioactivity studies of 1,2-dihydrobenzo[d]isothiazol-3-one-1,1-dioxide hydroxamic acid derivatives as novel histone deacetylase inhibitors. Bioorganic & Medicinal Chemistry. 22: 1529-38. PMID 24525003 DOI: 10.1016/J.Bmc.2014.01.045 |
0.359 |
|
| 2014 |
Wang J, Sun F, Han L, Hou X, Pan X, Liu R, Tang W, Fang H. Design, synthesis, and preliminary bioactivity studies of substituted purine hydroxamic acid derivatives as novel histone deacetylase (HDAC) inhibitors Medchemcomm. 5: 1887-1891. DOI: 10.1039/C4Md00203B |
0.363 |
|
| 2014 |
Wang H, Zhang W, Schienebeck CM, Bennett SR, Tang W. Intermolecular bromoesterification of conjugated enynes: an efficient synthesis of bromoallenes Organic Chemistry Frontiers. 1: 386-390. DOI: 10.1039/C3Qo00088E |
0.642 |
|
| 2014 |
Zheng S, Schienebeck CM, Zhang W, Wang H, Tang W. Cinchona Alkaloids as Organocatalysts in Enantioselective Halofunctionalization of Alkenes and Alkynes Asian Journal of Organic Chemistry. 3: 366-376. DOI: 10.1002/Ajoc.201400030 |
0.647 |
|
| 2013 |
Li X, Song W, Tang W. Rhodium-catalyzed tandem annulation and (5 + 1) cycloaddition: 3-hydroxy-1,4-enyne as the 5-carbon component. Journal of the American Chemical Society. 135: 16797-800. PMID 24164088 DOI: 10.1021/Ja408829Y |
0.397 |
|
| 2013 |
Shu XZ, Schienebeck CM, Song W, Guzei IA, Tang W. Transfer of chirality in the rhodium-catalyzed intramolecular [5+2] cycloaddition of 3-acyloxy-1,4-enynes (ACEs) and alkynes: synthesis of enantioenriched bicyclo[5.3.0]decatrienes. Angewandte Chemie (International Ed. in English). 52: 13601-5. PMID 24150975 DOI: 10.1002/Anie.201306919 |
0.622 |
|
| 2013 |
Liu N, Wang HY, Zhang W, Jia ZH, Guzei IA, Xu HD, Tang W. Stereoselective halocyclization of alkenes with N-acyl hemiaminal nucleophiles. Chirality. 25: 805-9. PMID 23946166 DOI: 10.1002/Chir.22219 |
0.604 |
|
| 2013 |
Zhang M, Liu N, Tang W. Stereoselective total synthesis of hainanolidol and harringtonolide via oxidopyrylium-based [5 + 2] cycloaddition. Journal of the American Chemical Society. 135: 12434-8. PMID 23930656 DOI: 10.1021/Ja406255J |
0.43 |
|
| 2013 |
Shu D, Winston-McPherson GN, Song W, Tang W. Platinum-catalyzed tandem indole annulation/arylation for the synthesis of diindolylmethanes and indolo[3,2-b]carbazoles. Organic Letters. 15: 4162-5. PMID 23909946 DOI: 10.1021/Ol4018408 |
0.409 |
|
| 2013 |
Xu X, Liu P, Shu XZ, Tang W, Houk KN. Rh-catalyzed (5+2) cycloadditions of 3-acyloxy-1,4-enynes and alkynes: computational study of mechanism, reactivity, and regioselectivity. Journal of the American Chemical Society. 135: 9271-4. PMID 23725341 DOI: 10.1021/Ja4036785 |
0.614 |
|
| 2013 |
Liu R, Winston-McPherson GN, Yang ZY, Zhou X, Song W, Guzei IA, Xu X, Tang W. Generation of rhodium(I) carbenes from ynamides and their reactions with alkynes and alkenes. Journal of the American Chemical Society. 135: 8201-4. PMID 23701315 DOI: 10.1021/Ja4047069 |
0.392 |
|
| 2013 |
Schienebeck CM, Robichaux PJ, Li X, Chen L, Tang W. Effect of ester on rhodium-catalyzed intermolecular [5+2] cycloaddition of 3-acyloxy-1,4-enynes and alkynes. Chemical Communications (Cambridge, England). 49: 2616-8. PMID 23435501 DOI: 10.1039/C3Cc40634B |
0.385 |
|
| 2013 |
Shu D, Song W, Li X, Tang W. Rhodium- and platinum-catalyzed [4+3] cycloaddition with concomitant indole annulation: synthesis of cyclohepta[b]indoles. Angewandte Chemie (International Ed. in English). 52: 3237-40. PMID 23401302 DOI: 10.1002/Anie.201209266 |
0.414 |
|
| 2013 |
Xu HD, Zhang RW, Li X, Huang S, Tang W, Hu WH. Rhodium-catalyzed chemo- and regioselective cross-dimerization of two terminal alkynes. Organic Letters. 15: 840-3. PMID 23356993 DOI: 10.1021/Ol303531M |
0.332 |
|
| 2013 |
Liu R, Zhang M, Winston-McPherson G, Tang W. Ring expansion of alkynyl cyclopropanes to highly substituted cyclobutenes via a N-sulfonyl-1,2,3-triazole intermediate. Chemical Communications (Cambridge, England). 49: 4376-8. PMID 22864054 DOI: 10.1039/C2Cc34609E |
0.413 |
|
| 2013 |
Fass DM, Reis SA, Ghosh B, Hennig KM, Joseph NF, Zhao WN, Nieland TJ, Guan JS, Kuhnle CE, Tang W, Barker DD, Mazitschek R, Schreiber SL, Tsai LH, Haggarty SJ. Crebinostat: a novel cognitive enhancer that inhibits histone deacetylase activity and modulates chromatin-mediated neuroplasticity. Neuropharmacology. 64: 81-96. PMID 22771460 DOI: 10.1016/J.Neuropharm.2012.06.043 |
0.615 |
|
| 2013 |
Zhang W, Liu N, Schienebeck CM, Zhou X, Izhar II, Guzei IA, Tang W. Enantioselective intermolecular bromoesterification of allylic sulfonamides Chemical Science. 4: 2652-2656. DOI: 10.1039/C3Sc50446H |
0.411 |
|
| 2013 |
Werness JB, Zhang W, Tang W. Stereoselective Addition of Halogen to Conjugated Enynes and Its Application in the Total Synthesis of (−)-Kumausallene Strategies and Tactics in Organic Synthesis. 9: 275-291. DOI: 10.1016/B978-0-08-099362-1.00010-2 |
0.441 |
|
| 2012 |
Shu XZ, Shu D, Schienebeck CM, Tang W. Rhodium-catalyzed acyloxy migration of propargylic esters in cycloadditions, inspiration from the recent "gold rush". Chemical Society Reviews. 41: 7698-711. PMID 22895533 DOI: 10.1039/C2Cs35235D |
0.608 |
|
| 2012 |
Shu D, Li X, Zhang M, Robichaux PJ, Guzei IA, Tang W. Rhodium-catalyzed carbonylation of cyclopropyl substituted propargyl esters: a tandem 1,3-acyloxy migration [5 + 1] cycloaddition. The Journal of Organic Chemistry. 77: 6463-72. PMID 22793991 DOI: 10.1021/Jo300973R |
0.449 |
|
| 2012 |
Zhang M, Tang W. Synthesis of functionalized cyclohexenone core of welwitindolinones via rhodium-catalyzed [5 + 1] cycloaddition. Organic Letters. 14: 3756-9. PMID 22783971 DOI: 10.1021/Ol301614V |
0.429 |
|
| 2012 |
Liu R, Zhang M, Wyche TP, Winston-McPherson GN, Bugni TS, Tang W. Stereoselective preparation of cyclobutanes with four different substituents: total synthesis and structural revision of pipercyclobutanamide A and piperchabamide G. Angewandte Chemie (International Ed. in English). 51: 7503-6. PMID 22715150 DOI: 10.1002/Anie.201203379 |
0.426 |
|
| 2012 |
Zhang W, Liu N, Schienebeck CM, Decloux K, Zheng S, Werness JB, Tang W. Catalytic enantioselective halolactonization of enynes and alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 7296-305. PMID 22549978 DOI: 10.1002/Chem.201103809 |
0.408 |
|
| 2012 |
Li X, Huang S, Schienebeck CM, Shu D, Tang W. Rhodium-catalyzed carbonylation of 3-acyloxy-1,4-enynes for the synthesis of cyclopentenones. Organic Letters. 14: 1584-7. PMID 22381143 DOI: 10.1021/Ol300330T |
0.421 |
|
| 2012 |
Shu XZ, Li X, Shu D, Huang S, Schienebeck CM, Zhou X, Robichaux PJ, Tang W. Rhodium-catalyzed intra- and intermolecular [5 + 2] cycloaddition of 3-acyloxy-1,4-enyne and alkyne with concomitant 1,2-acyloxy migration. Journal of the American Chemical Society. 134: 5211-21. PMID 22364320 DOI: 10.1021/Ja2109097 |
0.664 |
|
| 2012 |
Huang S, Li X, Lin CL, Guzei IA, Tang W. Rhodium-catalyzed 1,3-acyloxy migration and subsequent intramolecular [4+2] cycloaddition of vinylallene and unactivated alkyne. Chemical Communications (Cambridge, England). 48: 2204-6. PMID 22252254 DOI: 10.1039/C2Cc17406E |
0.43 |
|
| 2011 |
Li X, Zhang M, Shu D, Robichaux PJ, Huang S, Tang W. Rhodium-catalyzed ring expansion of cyclopropanes to seven-membered rings by 1,5 C-C bond migration. Angewandte Chemie (International Ed. in English). 50: 10421-4. PMID 21910200 DOI: 10.1002/Anie.201104861 |
0.358 |
|
| 2011 |
Shu XZ, Huang S, Shu D, Guzei IA, Tang W. Interception of a Rautenstrauch intermediate by alkynes for [5+2] cycloaddition: rhodium-catalyzed cycloisomerization of 3-acyloxy-4-ene-1,9-diynes to bicyclo[5.3.0]decatrienes. Angewandte Chemie (International Ed. in English). 50: 8153-6. PMID 21748834 DOI: 10.1002/Anie.201103136 |
0.635 |
|
| 2011 |
Werness JB, Tang W. Stereoselective total synthesis of (-)-kumausallene. Organic Letters. 13: 3664-6. PMID 21688862 DOI: 10.1021/Ol201477U |
0.444 |
|
| 2011 |
Tang W, Luo T, Greenberg EF, Bradner JE, Schreiber SL. Discovery of histone deacetylase 8 selective inhibitors. Bioorganic & Medicinal Chemistry Letters. 21: 2601-5. PMID 21334896 DOI: 10.1016/J.Bmcl.2011.01.134 |
0.718 |
|
| 2011 |
Shu D, Li X, Zhang M, Robichaux PJ, Tang W. Synthesis of highly functionalized cyclohexenone rings: rhodium-catalyzed 1,3-acyloxy migration and subsequent [5+1] cycloaddition. Angewandte Chemie (International Ed. in English). 50: 1346-9. PMID 21290509 DOI: 10.1002/Anie.201006881 |
0.454 |
|
| 2011 |
Werness JB, Tang W. Synthesis of (-)-Kumausallene Synfacts. 2011: 1042-1042. DOI: 10.1055/S-0030-1261141 |
0.378 |
|
| 2011 |
Liu N, Schienebeck CM, Collier MD, Tang W. Effect of halogenation reagents on halocyclization and Overman rearrangement of allylic trichloroacetimidates Tetrahedron Letters. 52: 6217-6219. DOI: 10.1016/J.Tetlet.2011.09.057 |
0.352 |
|
| 2011 |
Liu N, Werness JB, Guzei IA, Tang W. Intramolecular 1,4-addition of nitrogen nucleophile and bromine electrophile to conjugated 1,3-enyne Tetrahedron. 67: 4385-4390. DOI: 10.1016/J.Tet.2011.02.039 |
0.418 |
|
| 2011 |
Werness JB, Tang W. Synthesis of bromoallenyl pyrrolidines via 1,4-addition to 1,3-enynes Science China-Chemistry. 54: 56-60. DOI: 10.1007/S11426-010-4133-6 |
0.465 |
|
| 2010 |
Zhang W, Zheng S, Liu N, Werness JB, Guzei IA, Tang W. Enantioselective bromolactonization of conjugated (Z)-enynes. Journal of the American Chemical Society. 132: 3664-5. PMID 20192183 DOI: 10.1021/Ja100173W |
0.43 |
|
| 2009 |
Um JM, Xu H, Houk KN, Tang W. Thermodynamic control of the electrocyclic ring opening of cyclobutenes: C=X substituents at C-3 mask the kinetic torquoselectivity. Journal of the American Chemical Society. 131: 6664-5. PMID 19402639 DOI: 10.1021/Ja9016446 |
0.375 |
|
| 2009 |
Borowiak M, Maehr R, Chen S, Chen AE, Tang W, Fox JL, Schreiber SL, Melton DA. Small molecules efficiently direct endodermal differentiation of mouse and human embryonic stem cells. Cell Stem Cell. 4: 348-58. PMID 19341624 DOI: 10.1016/J.Stem.2009.01.014 |
0.461 |
|
| 2009 |
Patel V, Mazitschek R, Coleman B, Nguyen C, Urgaonkar S, Cortese J, Barker RH, Greenberg E, Tang W, Bradner JE, Schreiber SL, Duraisingh MT, Wirth DF, Clardy J. Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum. Journal of Medicinal Chemistry. 52: 2185-7. PMID 19317450 DOI: 10.1021/Jm801654Y |
0.599 |
|
| 2009 |
Zhang W, Xu H, Xu H, Tang W. DABCO-catalyzed 1,4-bromolactonization of conjugated enynes: highly stereoselective formation of a stereogenic center and an axially chiral allene. Journal of the American Chemical Society. 131: 3832-3. PMID 19245198 DOI: 10.1021/Ja8099008 |
0.46 |
|
| 2009 |
Fu QS, Boonchayaanant B, Tang W, Trost BM, Criddle CS. Simple menaquinones reduce carbon tetrachloride and iron (III). Biodegradation. 20: 109-16. PMID 18594993 DOI: 10.1007/S10532-008-9204-4 |
0.339 |
|
| 2009 |
Zhang W, Xu H, Tang W. Stereoselective Synthesis of Lactones From Conjugated Enynes Synfacts. 2009: 604-604. DOI: 10.1055/S-0029-1216700 |
0.423 |
|
| 2009 |
Zhang W, Werness JB, Tang W. Intramolecular hydroamination of conjugated enynes Tetrahedron. 65: 3090-3095. DOI: 10.1016/J.Tet.2008.09.045 |
0.373 |
|
| 2008 |
Xu H, Zhang W, Shu D, Werness JB, Tang W. Synthesis of cyclobutenes by highly selective transition-metal-catalyzed ring expansion of cyclopropanes. Angewandte Chemie (International Ed. in English). 47: 8933-6. PMID 18850597 DOI: 10.1002/Anie.200803910 |
0.365 |
|
| 2008 |
Zhang W, Werness JB, Tang W. Base-catalyzed intramolecular hydroamination of conjugated enynes. Organic Letters. 10: 2023-6. PMID 18435544 DOI: 10.1021/Ol800334M |
0.442 |
|
| 2007 |
Vegas AJ, Bradner JE, Tang W, McPherson OM, Greenberg EF, Koehler AN, Schreiber SL. Fluorous-based small-molecule microarrays for the discovery of histone deacetylase inhibitors. Angewandte Chemie (International Ed. in English). 46: 7960-4. PMID 17868168 DOI: 10.1002/Anie.200703198 |
0.763 |
|
| 2005 |
Trost BM, Tang W, Toste FD. Divergent enantioselective synthesis of (-)-galanthamine and (-)-morphine. Journal of the American Chemical Society. 127: 14785-803. PMID 16231933 DOI: 10.1021/Ja054449+ |
0.637 |
|
| 2003 |
Trost BM, Tang W. Migratory hydroamination: a facile enantioselective synthesis of benzomorphans. Journal of the American Chemical Society. 125: 8744-5. PMID 12862467 DOI: 10.1021/Ja0360539 |
0.535 |
|
| 2002 |
Trost BM, Tang W. Enantioselective synthesis of (-)-codeine and (-)-morphine. Journal of the American Chemical Society. 124: 14542-3. PMID 12465957 DOI: 10.1021/Ja0283394 |
0.505 |
|
| 2002 |
Trost BM, Tang W. An efficient enantioselective synthesis of (-)-galanthamine. Angewandte Chemie (International Ed. in English). 41: 2795-7. PMID 12203489 DOI: 10.1002/1521-3773(20020802)41:15<2795::Aid-Anie2795>3.0.Co;2-2 |
0.492 |
|
| 2001 |
Trost BM, Tang W. An enantioselective strategy to macrocyclic bisindolylmaleimides. An efficient formal synthesis of LY 333531. Organic Letters. 3: 3409-11. PMID 11594846 DOI: 10.1021/Ol016666V |
0.525 |
|
| 2000 |
Trost BM, Tang W, Schulte JL. Asymmetric synthesis of quaternary centers. Total synthesis of (-)-malyngolide. Organic Letters. 2: 4013-5. PMID 11112631 DOI: 10.1021/Ol006599P |
0.494 |
|
| 1998 |
Sun L, Li P, Amankulor N, Tang W, Landry DW, Zhao K. N-Alkoxy Analogues Of 3,4,5-Trihydroxypiperidine Journal of Organic Chemistry. 63: 6472-6475. DOI: 10.1021/Jo971535M |
0.358 |
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