Jie Wang - Publications

Affiliations: 
Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, Shanghai Shi, China 
Area:
Organic Chemistry

13 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
2021 Deng LM, Hu LJ, Bai YT, Wang J, Qin GQ, Song QY, Su JC, Huang XJ, Jiang RW, Tang W, Li YL, Li CC, Ye WC, Wang Y. Rhodomentosones A and B: Two Pairs of Enantiomeric Phloroglucinol Trimers from and Their Asymmetric Biomimetic Synthesis. Organic Letters. PMID 34032453 DOI: 10.1021/acs.orglett.1c01616  0.62
2019 Flood DT, Asai S, Zhang X, Wang J, Yoon L, Adams ZC, Dillingham BC, Sanchez BB, Vantourout JC, Flanagan ME, Piotrowski DW, Richardson PF, Green SA, Shenvi RA, Chen JS, et al. Expanding Reactivity in DNA-Encoded Library Synthesis via Reversible Binding of DNA to an Inert Quaternary Ammonium Support. Journal of the American Chemical Society. PMID 31136164 DOI: 10.1021/Jacs.9B03774  0.694
2018 Wang J, Shang M, Lundberg H, Feu KS, Hecker SJ, Qin T, Blackmond DG, Baran PS. Cu-Catalyzed Decarboxylative Borylation. Acs Catalysis. 8: 9537-9542. PMID 30505624 DOI: 10.1021/Acscatal.8B02928  0.727
2018 Wang J, Lundberg H, Asai S, Martín-Acosta P, Chen JS, Brown S, Farrell W, Dushin RG, O'Donnell CJ, Ratnayake AS, Richardson P, Liu Z, Qin T, Blackmond DG, Baran PS. Kinetically guided radical-based synthesis of C(sp)-C(sp) linkages on DNA. Proceedings of the National Academy of Sciences of the United States of America. PMID 29946037 DOI: 10.1073/Pnas.1806900115  0.725
2017 Li D, Yang D, Wang L, Liu X, Wang K, Wang J, Wang P, Liu Y, Zhu H, Wang R. An Efficient Nickel-Catalyzed Asymmetric Oxazole-Forming Ugi-Type Reaction for the Synthesis of Chiral Aryl-Substituted THIQ Rings. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28470882 DOI: 10.1002/chem.201700970  0.306
2017 Li C, Wang J, Barton LM, Yu S, Tian M, Peters DS, Kumar M, Yu AW, Johnson KA, Chatterjee AK, Yan M, Baran PS. Decarboxylative borylation. Science (New York, N.Y.). 356. PMID 28408721 DOI: 10.1126/science.aam7355  0.741
2017 Lopchuk JM, Fjelbye K, Kawamata Y, Malins LR, Pan CM, Gianatassio R, Wang J, Prieto L, Bradow J, Brandt TA, Collins MR, Elleraas J, Ewanicki J, Farrell W, Fadeyi OO, et al. Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity. Journal of the American Chemical Society. PMID 28140573 DOI: 10.1021/Jacs.6B13229  0.726
2016 Wang J, Qin T, Chen TG, Wimmer L, Edwards JT, Cornella J, Vokits B, Shaw SA, Baran PS. Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids. Angewandte Chemie (International Ed. in English). PMID 27380912 DOI: 10.1002/Anie.201605463  0.693
2016 Cornella J, Edwards JT, Qin T, Kawamura S, Wang J, Pan CM, Gianatassio R, Schmidt MA, Eastgate MD, Baran PS. Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters. Journal of the American Chemical Society. PMID 26835704 DOI: 10.1021/Jacs.6B00250  0.695
2016 Gianatassio R, Lopchuk JM, Wang J, Pan CM, Malins LR, Prieto L, Brandt TA, Collins MR, Gallego GM, Sach NW, Spangler JE, Zhu H, Zhu J, Baran PS. Strain-release amination. Science (New York, N.Y.). 351: 241-246. PMID 26816372 DOI: 10.1126/Science.Aad6252  0.72
2014 Wang XL, Lu YY, Wang J, Wang X, Yao HQ, Lin GQ, Sun BF. A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol. Organic & Biomolecular Chemistry. 12: 3562-6. PMID 24676561 DOI: 10.1039/C4Ob00046C  0.502
2013 Wang J, Chen SG, Sun BF, Lin GQ, Shang YJ. Collective total synthesis of englerin A and B, orientalol E and F, and oxyphyllol: application of the organocatalytic [4+3] cycloaddition reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2539-47. PMID 23292997 DOI: 10.1002/Chem.201203467  0.545
2012 Wang J, Sun BF, Cui K, Lin GQ. An efficient total synthesis of (-)-epothilone B. Organic Letters. 14: 6354-7. PMID 23214997 DOI: 10.1021/Ol303148G  0.501
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