Wei-Wei Liao - Related publications

2005-2006 Department of Organic Chemistry Jilin University, China, Changchun Shi, Jilin Sheng, China 
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24 most relevant papers in past 60 days:
Year Citation  Score
2022 Liao G, Zhang T, Jin L, Wang BJ, Xu CK, Lan Y, Zhao Y, Shi BF. Experimental and Computational Studies on the Directing Ability of Chalcogenoethers in Palladium-Catalyzed Atroposelective C-H Olefination and Allylation. Angewandte Chemie (International Ed. in English). PMID 34985788 DOI: 10.1002/anie.202115221   
2022 Min XL, Zhang XL, Yi W, He Y. Brønsted acid-enhanced copper-catalyzed atroposelective cycloisomerization to axially chiral arylquinolizones via dearomatization of pyridine. Nature Communications. 13: 373. PMID 35042873 DOI: 10.1038/s41467-022-27989-3   
2022 Yan JL, Maiti R, Ren SC, Tian W, Li T, Xu J, Mondal B, Jin Z, Chi YR. Carbene-catalyzed atroposelective synthesis of axially chiral styrenes. Nature Communications. 13: 84. PMID 35013298 DOI: 10.1038/s41467-021-27771-x   
2022 Yin C, Pan Y, Zhang X, Yin Q. Catalytic Asymmetric Hydrogenation of Tetrasubstituted Unsaturated Lactams: An Efficient Approach to Enantioenriched 3,4-Disubstituted Piperidines. Organic Letters. 24: 675-680. PMID 35005963 DOI: 10.1021/acs.orglett.1c04132   
2022 Tu Y, Yang JS, Lu K, Li CX, Zhao ZH, Zhang XM, Zhang FM. Chiral 1,2,3-Triazolium Salt Catalyzed Asymmetric Mono- and Dialkylation of 2,5-Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers. Angewandte Chemie (International Ed. in English). PMID 34981881 DOI: 10.1002/anie.202114129   
2022 Smedley CJ, Homer JA, Gialelis TL, Barrow AS, Koelln RA, Moses JE. Accelerated SuFEx Click Chemistry For Modular Synthesis. Angewandte Chemie (International Ed. in English). 61: e202112375. PMID 34755436 DOI: 10.1002/anie.202112375   
2022 Lu C, Ye M, Long L, Zheng Y, Liu J, Zhang Y, Chen Z. Synthesis of Unsymmetrical Diarylfumaronitriles via Tandem Michael Addition and Oxidation under KFe(CN)/O System. The Journal of Organic Chemistry. PMID 35014849 DOI: 10.1021/acs.joc.1c02498   
2022 Zhang WW, Liu CX, Yang P, Zhang SZ, Gu Q, You SL. Rhodium-Catalyzed Atroposelective C-H/C-H Cross-Coupling Reaction between 1-Aryl Isoquinoline Derivatives and Indolizines. Organic Letters. PMID 34985290 DOI: 10.1021/acs.orglett.1c04002   
2022 Bakthadoss M, Reddy TT, Agarwal V, Sharada DS. Ester-directed orthogonal dual C-H activation and aryl C-H alkenylation distal weak coordination. Chemical Communications (Cambridge, England). PMID 34994762 DOI: 10.1039/d1cc06097j   
2022 Nie FY, Cai YP, Song QH. Visible Light-Driven Decarboxylative Alkylation of Aldehydes via Electron Donor-Acceptor Complexes of Active Esters. The Journal of Organic Chemistry. PMID 34989227 DOI: 10.1021/acs.joc.1c02586   
2022 Zou W, Gao L, Cao J, Li Z, Li G, Wang G, Li S. Mechanistic Insight into Hydroboration of Imines from Combined Computational and Experimental Studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35018677 DOI: 10.1002/chem.202104004   
2022 Rozsar D, Formica M, Yamazaki K, Hamlin TA, Dixon DJ. Bifunctional Iminophosphorane-Catalyzed Enantioselective Sulfa-Michael Addition to Unactivated α,β-Unsaturated Amides. Journal of the American Chemical Society. PMID 34990142 DOI: 10.1021/jacs.1c11898   
2022 Patil NT, Das A. Enantioselective C-H Functionalization Reactions under Gold Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35014732 DOI: 10.1002/chem.202104371   
2022 Song H, Zhou H, Shen Y, Wang H, Song H, Cai X, Xu C. HFIP as Protonation Reagent and Solvent for Regioselective Alkylation of Indoles with All-Carbon Centers. The Journal of Organic Chemistry. PMID 35015536 DOI: 10.1021/acs.joc.1c02412   
2022 Sunagatullina AS, Lutter FH, Knochel P. Preparation of Primary and Secondary Dialkylmagnesiums by a Radical I/Mg-exchange Reaction Using sBu2Mg in Toluene. Angewandte Chemie (International Ed. in English). PMID 35044040 DOI: 10.1002/anie.202116625   
2022 Yang P, Wang Q, Cui BH, Zhang XD, Liu H, Zhang YY, Liu JL, Huang WY, Liang RX, Jia YX. Enantioselective Dearomative [3 + 2] Umpolung Annulation of -Heteroarenes with Alkynes. Journal of the American Chemical Society. PMID 35007081 DOI: 10.1021/jacs.1c11092   
2022 Alomari K, Sai Pavan Chakravarthy N, Duchadeau B, Ermanis K, Clarke PA. Enantioselective "clip-cycle" synthesis of di-, tri- and spiro-substituted tetrahydropyrans. Organic & Biomolecular Chemistry. PMID 35044408 DOI: 10.1039/d2ob00023g   
2022 Hao D, Yang Z, Liu Y, Li Y, Li C, Gu Y, Vaccaro L, Liu J, Liu P. Pd-Catalyzed direct C-H arylation of pyrrolo[1,2-]quinoxalines. Organic & Biomolecular Chemistry. PMID 34994375 DOI: 10.1039/d1ob02248b   
2022 Chen L, Wang Z, Wang Y, Hao L, Xu X, Wu G, Ji Y. Rhodium(III)-catalyzed cascade C-H functionalization/annulation of sulfoximines with iodonium ylides for the synthesis of cyclohexanone-1,2-benzothiazines. Organic & Biomolecular Chemistry. PMID 35018957 DOI: 10.1039/d1ob02110a   
2022 Dasgupta A, Richards E, Melen RL. Triarylborane Catalyzed Carbene Transfer Reactions Using Diazo Precursors. Acs Catalysis. 12: 442-452. PMID 35028191 DOI: 10.1021/acscatal.1c04746   
2022 Hao MY, Huang MH, Gu XY, Zhang TS, Zhu XT, Hao WJ, Jiang B. Diastereoselective Generation of C-Azlactonized 2-Chromenes via Brønsted Acid-Catalyzed Oxo-Cyclization of Propargyl Alcohols. The Journal of Organic Chemistry. PMID 35000383 DOI: 10.1021/acs.joc.1c02299   
2022 Sun SZ, Cai YM, Zhang DL, Wang JB, Yao HQ, Rui XY, Martin R, Shang M. Enantioselective Deaminative Alkylation of Amino Acid Derivatives with Unactivated Olefins. Journal of the American Chemical Society. PMID 35029378 DOI: 10.1021/jacs.1c12350   
2022 Panda TK, Kumar R, Rawal P, Banerjee I, Nayek HP, Gupta P, Panda TK. Catalytic Hydroboration and Reductive Amination of Carbonyl Compounds by HBpin using a Zinc Promoter. Chemistry, An Asian Journal. PMID 35020275 DOI: 10.1002/asia.202200013   
2022 Lo A, Gutierrez DA, Toth-Williams G, Fettinger JC, Shaw JT. 1,3-Asymmetric Induction in Diastereoselective Allylations of Chiral -Tosyl Imines. The Journal of Organic Chemistry. PMID 35029404 DOI: 10.1021/acs.joc.1c02691