Hengbin Wang, Ph.D. - Publications

Affiliations: 
2012 Chemistry Emory University, Atlanta, GA 
Area:
synthesis of biologically active natural products

16 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
2019 Vogt DB, Seath CP, Wang H, Jui NT. Selective C-F Functionalization of Unactivated Trifluoromethylarenes. Journal of the American Chemical Society. PMID 31369264 DOI: 10.1021/Jacs.9B06004  0.462
2017 Gilbert MM, DeMars MD, Yang S, Grandner JM, Wang S, Wang H, Narayan ARH, Sherman DH, Houk KN, Montgomery J. Synthesis of Diverse 11- and 12-Membered Macrolactones from a Common Linear Substrate Using a Single Biocatalyst. Acs Central Science. 3: 1304-1310. PMID 29296671 DOI: 10.1021/Acscentsci.7B00450  0.43
2017 Wang H, Jui NT. Catalytic Defluoroalkylation of Trifluoromethylaromatics with Unactivated Alkenes. Journal of the American Chemical Society. PMID 29256607 DOI: 10.1021/Jacs.7B12590  0.429
2017 Wang H, Lu G, Sormunen GJ, Malik HA, Liu P, Montgomery J. NHC Ligands Tailored for Simultaneous Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings. Journal of the American Chemical Society. PMID 28621131 DOI: 10.1021/Jacs.7B04583  0.446
2017 Aycock RA, Wang H, Jui NT. A mild catalytic system for radical conjugate addition of nitrogen heterocycles. Chemical Science. 8: 3121-3125. PMID 28507687 DOI: 10.1039/C7Sc00243B  0.355
2017 Li X, Wang H, Schneider JA, Wei Z, Lai W, Huang W, Wudl F, Zheng Y. Catalyst-free one-step synthesis of ortho-tetraaryl perylene diimides for efficient OPV non-fullerene acceptors Journal of Materials Chemistry C. 5: 2781-2785. DOI: 10.1039/C7Tc00263G  0.378
2015 Jackson EP, Malik HA, Sormunen GJ, Baxter RD, Liu P, Wang H, Shareef AR, Montgomery J. Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive Couplings. Accounts of Chemical Research. 48: 1736-45. PMID 25965694 DOI: 10.1021/Acs.Accounts.5B00096  0.476
2015 Wang H, Negretti S, Knauff AR, Montgomery J. Exo-selective reductive macrocyclization of ynals. Organic Letters. 17: 1493-6. PMID 25746060 DOI: 10.1021/Acs.Orglett.5B00381  0.679
2014 Lu P, Mailyan A, Gu Z, Guptill DM, Wang H, Davies HM, Zakarian A. Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalization. Journal of the American Chemical Society. 136: 17738-49. PMID 25409033 DOI: 10.1021/Ja510573V  0.721
2014 Fu L, Wang H, Davies HM. Role of ortho-substituents on rhodium-catalyzed asymmetric synthesis of β-lactones by intramolecular C-H insertions of aryldiazoacetates. Organic Letters. 16: 3036-9. PMID 24840720 DOI: 10.1021/Ol5011505  0.629
2014 Lu P, Mailyan A, Gu Z, Guptill DM, Wang H, Davies HML, Zakarian A. Enantioselective synthesis of (-)-maoecrystal v by enantiodetermining C-H functionalization Journal of the American Chemical Society. 136: 17738-17749. DOI: 10.1021/ja510573v  0.703
2013 Wang H, Guptill DM, Alvarez AV, Musaev DG, Davies HM. Rhodium-catalyzed enantioselective cyclopropanation of electron deficient alkenes. Chemical Science (Royal Society of Chemistry : 2010). 4: 2844-2850. PMID 24049630 DOI: 10.1039/C3Sc50425E  0.707
2013 Wang H, Li G, Engle KM, Yu JQ, Davies HM. Sequential C-H functionalization reactions for the enantioselective synthesis of highly functionalized 2,3-dihydrobenzofurans. Journal of the American Chemical Society. 135: 6774-7. PMID 23600441 DOI: 10.1021/Ja401731D  0.636
2011 Wang H, Denton JR, Davies HM. Sequential rhodium-, silver-, and gold-catalyzed synthesis of fused dihydrofurans. Organic Letters. 13: 4316-9. PMID 21770400 DOI: 10.1021/Ol2016548  0.714
2011 Wang H, Denton JR, Davies HML. Sequential rhodium-, silver-, and gold-catalyzed synthesis of fused dihydrofurans Organic Letters. 13: 4316-4319. DOI: 10.1021/ol2016548  0.679
2007 Li Y, Yin G, Wei W, Wang H, Jiang S, Zhu D, Du W. Interactions of Lycopodium alkaloids with acetylcholinesterase investigated by 1H NMR relaxation rate. Biophysical Chemistry. 129: 212-7. PMID 17601647 DOI: 10.1016/J.Bpc.2007.05.020  0.316
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