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Liang Wang - Publications

Affiliations: 
Qingdao Agricultral University 
Area:
Synthetic Chemistry
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25 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 Sun Z, Hou R, Li SS, Wang X, Wang L, Hu F, Guo FW. Controllable Synthesis of - and -Containing Heterocycles via Formal [3 + 2] and [5 + 2] Cyclizations. Organic Letters. PMID 38157254 DOI: 10.1021/acs.orglett.3c03227  0.309
2023 Li L, Li P, Li T, Zhang M, Liu W, Li J, Wang L, Chen Y. Synthesis of the ABC ring system of kadlongilactones. Organic & Biomolecular Chemistry. PMID 36749621 DOI: 10.1039/d2ob01701f  0.349
2018 Wen H, Cao W, Liu Y, Wang L, Chen P, Tang Y. Metal-Free [2 + 2 + 2] Cycloaddition of Ynamide-Nitriles with Ynamides: A Highly Regio- and Chemoselective Synthesis of δ-Carboline Derivatives. The Journal of Organic Chemistry. PMID 30353730 DOI: 10.1021/Acs.Joc.8B02112  0.304
2018 Shen YB, Li SS, Wang L, An XD, Liu Q, Liu X, Xiao J. Organocatalytic Dearomative [4 + 2] Cycloadditions of Biomass-Derived 2,5-Dimethylfuran with ortho-Quinone Methides: Access to Multisubstituted Chromanes. Organic Letters. PMID 30212223 DOI: 10.1021/Acs.Orglett.8B02448  0.342
2018 Mao Y, Liu Y, Hu Y, Wang L, Zhang S, Wang W. Pd-Catalyzed Debenzylation and Deallylation of Ethers and Esters with Sodium Hydride Acs Catalysis. 8: 3016-3020. DOI: 10.1021/Acscatal.8B00185  0.305
2017 Li SS, Zhou L, Wang L, Zhao H, Yu L, Xiao J. Organocatalytic C(sp3)-H Functionalization via Carbocation-Initiated Cascade [1,5]-Hydride Transfer/Cyclization: Synthesis of Dihydrodibenzo[b,e]azepines. Organic Letters. PMID 29239184 DOI: 10.1021/Acs.Orglett.7B03492  0.311
2016 Liu J, Wang L, Wang X, Xu L, Hao Z, Xiao J. Fluorinated alcohol-mediated [4 + 3] cycloaddition reaction of indolyl alcohols with cyclopentadiene. Organic & Biomolecular Chemistry. PMID 27886328 DOI: 10.1039/C6Ob01953F  0.338
2016 Dong H, Xu L, Li SS, Wang L, Shao CL, Xiao J. Facile Synthesis of Azaarene-substituted Hydroxycoumarins Possessing High Biological Activities via Three-Component C(sp3)-H Functionalization. Acs Combinatorial Science. PMID 27518450 DOI: 10.1021/Acscombsci.6B00082  0.309
2016 Wang L, Xiao J, Zhao H, Wang X. Regioselective Michael Addition of Anthrone to Methylene­indolinones Synthesis. 48: 2112-2120. DOI: 10.1055/S-0035-1561593  0.343
2016 Zhao H, Xiao M, Xu L, Wang L, Xiao J. Bifunctional thiourea catalyzed asymmetric Michael addition of anthrone to methyleneindolinones Rsc Advances. 6: 38558-38562. DOI: 10.1039/C5Ra21614A  0.359
2016 Xiao J, Wen H, Wang L, Xu L, Hao Z, Shao CL, Wang CY. Catalyst-free dehydrative SN1-type reaction of indolyl alcohols with diverse nucleophiles "on water" Green Chemistry. 18: 1032-1037. DOI: 10.1039/C5Gc01838B  0.323
2016 Fu S, Wang L, Dong H, Yu J, Xu L, Xiao J. Facile synthesis of 2-alkenylazaarenes via dehydrative coupling of 2-methylazaarenes with aldehydes ‘on water’ Tetrahedron Letters. 57: 4533-4536. DOI: 10.1016/J.Tetlet.2016.08.065  0.317
2016 Zhang X, Li S, Wang L, Xu L, Xiao J, Liu Z. 2-Methylquinoline promoted oxidative ring-opening of N-sulfonyl aziridines with DMSO: facile synthesis of α-amino aryl ketones Tetrahedron. 72: 8073-8077. DOI: 10.1016/J.Tet.2016.10.041  0.312
2016 Liu J, Wang X, Xu L, Hao Z, Wang L, Xiao J. One step synthesis of 2-alkenylchromanes via inverse electron-demand Hetero-Diels–Alder reaction of o -quinone methide with unactivated dienes Tetrahedron. 72: 7642-7649. DOI: 10.1016/J.Tet.2016.10.027  0.329
2015 Wang X, Liu J, Xu L, Hao Z, Wang L, Xiao J. Friedel-Crafts alkylation of heteroarenes and arenes with indolyl alcohols for construction of 3,3-disubstituted oxindoles Rsc Advances. 5: 101713-101717. DOI: 10.1039/C5Ra21919A  0.336
2015 Wen H, Wang L, Xu L, Hao Z, Shao CL, Wang CY, Xiao J. Fluorinated Alcohol-Mediated SN1-Type Reaction of Indolyl Alcohols with Diverse Nucleophiles Advanced Synthesis and Catalysis. 357: 4023-4030. DOI: 10.1002/Adsc.201500500  0.351
2014 Shao Z, Xu L, Wang L, Wei H, Xiao J. Catalyst-free tandem Michael addition/decarboxylation of (thio)coumarin-3-carboxylic acids with indoles: facile synthesis of indole-3-substituted 3,4-dihydro(thio)coumarins. Organic & Biomolecular Chemistry. 12: 2185-8. PMID 24589942 DOI: 10.1039/C3Ob42582G  0.323
2014 Xu L, Shao Z, Wang L, Xiao J. Tandem sp3 C-H functionlization/decarboxylation of 2-alkylazaarenes with coumarin-3-carboxylic acids. Organic Letters. 16: 796-9. PMID 24437668 DOI: 10.1021/Ol403541G  0.338
2014 Shao Z, Wang L, Xu L, Zhao H, Xiao J. Facile synthesis of azaarene-2-substituted chromanone derivatives via tandem sp3 C–H functionalization/decarboxylation of azaarenes with 4-oxo-4H-chromene-3-carboxylic acid Rsc Adv.. 4: 53188-53191. DOI: 10.1039/C4Ra09338K  0.308
2013 Tang B, Wang L, Menche D. Diastereoselective synthesis of 1,3- Syn -oxazines via a tandem hemiaminalization and Tsuji-Trost reaction Synlett. 24: 625-629. DOI: 10.1055/S-0032-1318300  0.592
2012 Wang L, Menche D. Construction of multisubstituted tetrahydropyrans by a domino oxa-Michael/Tsuji-Trost reaction. The Journal of Organic Chemistry. 77: 10811-23. PMID 23140526 DOI: 10.1021/Jo302102X  0.581
2012 Wang L, Menche D. Concise synthesis of acetal-protected syn 1,3-diols by a tandem hemiacetal formation/Tsuji-Trost reaction. Angewandte Chemie (International Ed. in English). 51: 9425-7. PMID 22893592 DOI: 10.1002/Anie.201203911  0.608
2012 Wang L, Menche D. Kurze Synthese von Acetal-geschützten 1,3-syn-Diolen durch einen Tandemprozess aus Halbacetalbildung und Tsuji-Trost-Reaktion Angewandte Chemie. 124: 9559-9562. DOI: 10.1002/Ange.201203911  0.54
2010 Wang L, Li P, Menche D. Concise synthesis of tetrahydropyrans by a tandem oxa-Michael/Tsuji-Trost reaction. Angewandte Chemie (International Ed. in English). 49: 9270-3. PMID 20979071 DOI: 10.1002/Anie.201003304  0.62
2010 Wang L, Li P, Menche D. Kurze Synthese von Tetrahydropyranen durch eine Oxa-Michael-Tsuji-Trost-Tandemreaktion Angewandte Chemie. 122: 9456-9460. DOI: 10.1002/Ange.201003304  0.583
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