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Dawen Niu - Publications

Affiliations: 
Sichuan University, Chengdu Shi, Sichuan Sheng, China 
Website:
http://www.theniugroup.com/index.php
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38 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 Shang W, Niu D. Radical Pathway Glycosylation Empowered by Bench-Stable Glycosyl Donors. Accounts of Chemical Research. PMID 37594017 DOI: 10.1021/acs.accounts.3c00374  0.376
2023 Zuo H, Zhang C, Zhang Y, Niu D. Base-Promoted Glycosylation Allows Protecting Group-Free and Stereoselective O-Glycosylation of Carboxylic Acids. Angewandte Chemie (International Ed. in English). e202309887. PMID 37590127 DOI: 10.1002/anie.202309887  0.38
2023 Xu S, Zhang W, Li C, Li Y, Zeng H, Wang Y, Zhang Y, Niu D. Generation and Use of Glycosyl Radicals under Acidic Conditions: Glycosyl Sulfinates as Precursors. Angewandte Chemie (International Ed. in English). PMID 36760072 DOI: 10.1002/anie.202218303  0.389
2022 Xie D, Wang Y, Zhang X, Fu Z, Niu D. Alkyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives. Angewandte Chemie (International Ed. in English). PMID 35641436 DOI: 10.1002/anie.202204922  0.409
2022 Sun HL, Wu B, Liu DQ, Yu ZD, Wang JJ, Liu Q, Liu X, Niu D, Dou JH, Zhu R. Synthesis of Polydiynes an Unexpected Dimerization/Polymerization Sequence of C3 Propargylic Electrophiles. Journal of the American Chemical Society. PMID 35522220 DOI: 10.1021/jacs.2c02816  0.471
2022 Pu X, Dang QD, Yang L, Zhang X, Niu D. Doubly stereoconvergent construction of vicinal all-carbon quaternary and tertiary stereocenters by Cu/Mg-catalyzed propargylic substitution. Nature Communications. 13: 2457. PMID 35508476 DOI: 10.1038/s41467-022-29986-y  0.407
2022 Zhang C, Zuo H, Lee GY, Zou Y, Dang QD, Houk KN, Niu D. Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation. Nature Chemistry. PMID 35410373 DOI: 10.1038/s41557-022-00918-z  0.328
2021 Gong L, Zhang Q, Xie D, Zhang W, Xu SY, Zhang X, Niu D. Selective synthesis of enol ethers nickel-catalyzed cross coupling of α-oxy-vinylsulfones with alkylzinc reagents. Chemical Communications (Cambridge, England). PMID 34734604 DOI: 10.1039/d1cc05347g  0.398
2021 Wan LQ, Zhang X, Zou Y, Shi R, Cao JG, Xu SY, Deng LF, Zhou L, Gong Y, Shu X, Lee GY, Ren H, Dai L, Qi S, Houk KN, ... Niu D, et al. Nonenzymatic Stereoselective -Glycosylation of Polypeptides and Proteins. Journal of the American Chemical Society. PMID 34323481 DOI: 10.1021/jacs.1c05156  0.386
2021 Wan LQ, Cao JG, Niu D, Zhang X. Cobalt-Catalyzed Umpolung Alkylation of Imines To Generate α-Branched Aliphatic Amines. Organic Letters. PMID 33974795 DOI: 10.1021/acs.orglett.1c00835  0.424
2020 Shang W, Su SN, Shi R, Mou ZD, Yu GQ, Zhang X, Niu D. Generation of Glycosyl Radicals from Glycosyl Sulfoxides and Its Use in the Synthesis of C-linked Glycoconjugates. Angewandte Chemie (International Ed. in English). PMID 32935426 DOI: 10.1002/Anie.202009828  0.467
2019 Yang L, Pu X, Niu D, Fu Z, Zhang X. Copper-Catalyzed Asymmetric Propargylation of Indolizines. Organic Letters. PMID 31638825 DOI: 10.1021/Acs.Orglett.9B03032  0.329
2019 Wang Y, Deng LF, Zhang X, Niu D. Catalytic Asymmetric Synthesis of α-Tetrasubstituted α-Trifluoromethyl Homoallylic Amines by Ir-Catalyzed Umpolung Allylation of Imines. Organic Letters. PMID 31418581 DOI: 10.1021/Acs.Orglett.9B02550  0.48
2019 Gong L, Sun H, Deng LF, Zhang X, Liu J, Yang S, Niu D. Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Oxo-Vinylsulfones to Prepare C-Aryl Glycals and Acyclic Vinyl Ethers. Journal of the American Chemical Society. PMID 31025860 DOI: 10.1021/Jacs.9B02312  0.479
2019 Shang W, He B, Niu D. Ligand-controlled, transition-metal catalyzed site-selective modification of glycosides. Carbohydrate Research. 474: 16-33. PMID 30703629 DOI: 10.1016/J.Carres.2019.01.006  0.327
2019 Cao C, He B, Fu Z, Niu D. Synthesis of β3-Amino Esters by Iridium-Catalyzed Asymmetric Allylic Alkylation Reaction Organic Process Research & Development. 23: 1758-1761. DOI: 10.1021/Acs.Oprd.9B00280  0.388
2018 Fu Z, Deng N, Su SN, Li H, Li RZ, Zhang X, Liu J, Niu D. Diastereo- and enantioselective propargylations of 5H-thiazol-4-ones and 5H-oxazol-4-ones as enabled by Cu/Zn and Cu/Ti catalysis. Angewandte Chemie (International Ed. in English). PMID 30232833 DOI: 10.1002/Anie.201809391  0.427
2018 Zhan M, Pu X, He B, Niu D, Zhang X. Intramolecular Umpolung Allylation of Imines. Organic Letters. PMID 30203981 DOI: 10.1021/Acs.Orglett.8B02536  0.408
2018 Sun HB, Gong L, Tian YB, Wu JG, Zhang X, Liu J, Fu Z, Niu D. Metal- and Base-Free Room-Temperature Amination of Organoboronic Acids with N-Alkyl Hydroxylamines. Angewandte Chemie (International Ed. in English). PMID 29736974 DOI: 10.1002/Anie.201802782  0.38
2017 Niu D, Shang W, Mou ZD, Tang H, Zhang X, Liu J, Fu Z. Site-Selective O-Arylation of Glycosides. Angewandte Chemie (International Ed. in English). PMID 29125221 DOI: 10.1002/Anie.201710310  0.379
2017 Li RZ, Tang H, Yang KR, Wan LQ, Zhang X, Liu J, Fu Z, Niu D. Enantioselective Propargylation of Polyols and Desymmetrization of meso 1,2-Diols by Copper/Borinic Acid Dual Catalysis. Angewandte Chemie (International Ed. in English). PMID 28523904 DOI: 10.1002/Anie.201703029  0.446
2017 Niu D, Wan L, Tian L, Liu J. Iridium-Catalyzed Asymmetric Umpolung Allylation of N-Fluor­enyl Imines to Prepare 1,4-Disubstituted Homoallylic Amines Synlett. 28: 2051-2056. DOI: 10.1055/S-0036-1588514  0.589
2017 Li R, Tang H, Wan L, Zhang X, Fu Z, Liu J, Yang S, Jia D, Niu D. Site-Divergent Delivery of Terminal Propargyls to Carbohydrates by Synergistic Catalysis Chem. 3: 834-845. DOI: 10.1016/J.Chempr.2017.09.007  0.374
2016 Zhang J, Niu D, Brinker VA, Hoye TR. The Phenol-Ene Reaction: Biaryl Synthesis via Trapping Reactions between HDDA-Generated Benzynes and Phenolics. Organic Letters. PMID 27767316 DOI: 10.1021/Acs.Orglett.6B02830  0.71
2016 Liu J, Cao CG, Sun HB, Zhang X, Niu D. Catalytic Asymmetric Umpolung Allylation of Imines. Journal of the American Chemical Society. PMID 27643490 DOI: 10.1021/Jacs.6B05288  0.458
2016 Wang T, Niu D, Hoye TR. The hexadehydro-Diels-Alder (HDDA) cycloisomerization reaction proceeds by a stepwise mechanism. Journal of the American Chemical Society. PMID 27266843 DOI: 10.1021/Jacs.6B03786  0.627
2016 Yang JC, Niu D, Karsten BP, Lima F, Buchwald SL. Use of a "Catalytic" Cosolvent, N,N-Dimethyl Octanamide, Allows the Flow Synthesis of Imatinib with no Solvent Switch. Angewandte Chemie (International Ed. in English). 55: 2531-5. PMID 26756279 DOI: 10.1002/Anie.201509922  0.471
2016 Zhan M, Li RZ, Mou ZD, Cao CG, Liu J, Chen YW, Niu D. Silver-Assisted, Iridium-Catalyzed Allylation of Bis[(pinacolato)boryl]methane Allows the Synthesis of Enantioenriched Homoallylic Organoboronic Esters Acs Catalysis. 6: 3381-3386. DOI: 10.1021/Acscatal.6B00719  0.464
2015 Niu D, Buchwald SL. Design of Modified Amine Transfer Reagents Allows the Synthesis of α-Chiral Secondary Amines via CuH-Catalyzed Hydroamination. Journal of the American Chemical Society. 137: 9716-21. PMID 26144542 DOI: 10.1021/Jacs.5B05446  0.583
2015 Yang Y, Shi SL, Niu D, Liu P, Buchwald SL. ORGANIC CHEMISTRY. Catalytic asymmetric hydroamination of unactivated internal olefins to aliphatic amines. Science (New York, N.Y.). 349: 62-6. PMID 26138973 DOI: 10.1126/Science.Aab3753  0.725
2015 Yang Y, Shi S, Niu D, Liu P, Buchwald SL. ChemInform Abstract: Catalytic Asymmetric Hydroamination of Unactivated Internal Olefins to Aliphatic Amines. Cheminform. 46: no-no. DOI: 10.1002/chin.201549026  0.476
2014 Willoughby PH, Niu D, Wang T, Haj MK, Cramer CJ, Hoye TR. Mechanism of the reactions of alcohols with o-benzynes. Journal of the American Chemical Society. 136: 13657-65. PMID 25232890 DOI: 10.1021/Ja502595M  0.746
2014 Niu D, Hoye TR. The aromatic ene reaction. Nature Chemistry. 6: 34-40. PMID 24345944 DOI: 10.1038/Nchem.1797  0.721
2014 Niu D, Wang T, Woods BP, Hoye TR. Dichlorination of (hexadehydro-Diels-Alder generated) benzynes and a protocol for interrogating the kinetic order of bimolecular aryne trapping reactions. Organic Letters. 16: 254-7. PMID 24329102 DOI: 10.1021/Ol403258C  0.781
2013 Niu D, Willoughby PH, Woods BP, Baire B, Hoye TR. Alkane desaturation by concerted double hydrogen atom transfer to benzyne. Nature. 501: 531-4. PMID 24067712 DOI: 10.1038/Nature12492  0.722
2013 Baire B, Niu D, Willoughby PH, Woods BP, Hoye TR. Synthesis of complex benzenoids via the intermediate generation of o-benzynes through the hexadehydro-Diels-Alder reaction. Nature Protocols. 8: 501-8. PMID 23411632 DOI: 10.1038/Nprot.2013.017  0.725
2012 Hoye TR, Baire B, Niu D, Willoughby PH, Woods BP. The hexadehydro-Diels-Alder reaction. Nature. 490: 208-12. PMID 23060191 DOI: 10.1038/Nature11518  0.729
2012 Niu D, Hoye TR. A concise total synthesis of (±)- and (-)-okilactomycin D. Organic Letters. 14: 828-31. PMID 22273402 DOI: 10.1021/Ol203355G  0.59
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