2017

180.Visible-Light Photocatalytic Decarboxylative Alkyl Radical Addition Cascade for Synthesis of Benzazepine Derivatives

Zhao Y.; Chen, J.-R.; Xiao, W.-J.*

Org. Lett., 2018, 20, 224-227

DOI: 10.1021/acs.orglett.7b03588

179.Visible Light-Driven Iminyl Radical-Mediated C-C Single Bond Cleavage/Radical Addition Cascade of Oxime Esters

Yu, X.-Y.; Chen,J.-R.*; Wang, P.-Z.; Yang, M.-N.; Liang, D.; Xiao, W.-J.*

Angew. Chem. Int. Ed., 2018, 57, 738-743

DOI:10.1002/anie.201710618

178.Biologically Inspired Ligand Design for Asymmetric Dia-stereodivergent 1,3-Dipolar Cycloaddition

Feng, B.; Chen, J.-R.; Yang, Y.-F.; Lu, B.; Xiao, W.-J.*

Chem. Eur. J., 2018, 24, 1714-1719

DOI: 10.1002/chem.201705301

177.Synthesis of Polysubstituted Pyrroles through a Formal [4 + 1] Cycloaddition/E1cb Elimination/Aromatization Sequence of Sulfur Ylides and α,β-Unsaturated Imines

Cheng, B.-Y.; Wang, Y.-N.; Li, T.-R.; Lu, L.-Q.*; Xiao, W.-J.*

J. Org. Chem.,2017,82, 12134–12140.

DOI:10.1021/acs.joc.7b01931

176.Catalyst- ad Oxidant-Free Desulfonative C-P Couplings for the Synthesis of Phosphine Oxides and Phosphonates

Guo,H.-M.; Zhou,Q.-Q.; Jiang, X.; Shi, D.-Q.*; Xiao, W.-J.*

Adv.Synth.Catal., 2017, 359, 4141-4146.

DOI: 10.1002/adsc.201700886

175. Sequential Visible-Light Photoactivation and Palladium Catalysis Enabling Enantioselective [4+2] Cycloadditions

Li, M.-M.1; Wei, Y.1; Liu,J.; Chen, H-W.; Lu, L.-Q.*; Xiao, W.-J.

J. Am. Chem. Soc., 2017, 139, 14707-14713.

DOI: 10.1021/jacs.7b08310

174. Synthesis of Dihydropyrazoles via Ligand-Free Pd-Catalyzed Alkene Aminoarylation of Unsaturated Hydrazones with Diaryliodonium Salts

Yang,M.-N.; Yan, D.-M.; Zhao, Q.-Q.; Chen, J.-R.*; Xiao, W.-J.*

Org. Lett., 2017, 19, 5208–5211

DOI:10.1021/acs.orglett.7b02480

173.Enantioconvergent Copper Catalysis: In Situ Generation of the Chiral Phosphorus Ylide and Its Wittig Reactions

Zhang, K.1; Lu, L.-Q.1; Yao, S.; Chen, J.-R.; Shi, D.-Q.; Xiao, W.-J.*

J. Am. Chem. Soc., 2017, 139, 12847–12854.

DOI:10.1021/jacs.7b08207

172.Divergent Synthesis of Polycyclic Indolines: Copper-Catalyzed Cascade Reactions of Propargylic Carbamates and Indoles

Li, T.-R.; Lu, L.-Q.*; Wang, Y.-N.; Wang, B.-C.; Xiao, W.-J.*

Org. Lett., 2017, 19, 4098–4101.

DOI:10.1021/acs.orglett.7b01903

171. Hydrogen Bond Direction Enables Palladium-Catalyzed Branch- and Enantioselective Allylic Aminations and Beyond

Wang, Y.-N.;Wang, B.-C.;Zhang, M.-M.;Gao, X.-W.;Li, T-R;Lu, L.-Q.*; Xiao, W.-J.

Org. Lett., 2017, 19, 4094–4097.

DOI:10.1021/acs.orglett.7b01794

170. Photocatalytic Hydrazonyl Radical-Mediated RadicalC yclization/Allylation Cascade: Synthesis of Dihydropyrazoles and Tetrahydropyridazines

Zhao, Q.-Q.; Chen, J.; Yan, D.-M.; Chen, J.-R.;* Xiao, W.-J.*

Org. Lett., 2017, 19, 3620–3623.

DOI:10.1021/acs.orglett.7b01609

169.Visible Light-Driven Aza-ortho-Quinone Methide Generation Enables a Multicomponent Reaction

Liu, Y.-Y.; Yu, X.-Y.; Chen, J.-R.;* Qiao, M.-M.; Qi, X.-T.; Shi, D.-Q.; Xiao, W.-J. *

Angew. Chem. Int. Ed. 2017, 56, 9527-9531.

DOI: 10.1002/anie.201704690

168.Beyond sulfide-centric catalysis: recent advances in the catalytic cyclization reactions of sulfur ylides

Lu, L.-Q. *; Li, T.-R.; Wang, Q.; Xiao, W.-J.*

Chem. Soc. Rev., 2017, 46, 4135-4149.

DOI: 10.1039/c6cs00276e

167. Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes

Chen, D,-Z.; Chen, J.-R.*; Xiao, W.-J.*

Org. Chem. Front., 2017, 4, 1289-1293.

DOI: 10.1039/C7QO00163K

166. Photocascade Catalysis: A New Strategy for Cascade Reactions

Chen, J.-R.; Yan, D.-M.; Wei, Q.; Xiao, W.-J.*

ChemPhotoChem, 2017, 1, 148-158.

DOI: 10.1002/cptc.201700008

165. Controllable Remote C-H Bond Functionalization by Visible-Light Photocatalysis

Hu, X.-Q.; Chen, J.-R.*; Xiao, W.-J.*

Angew. Chem. Int. Ed., 2017, 13, 1960-1962.

DOI: 10.1002/ange.201611463

164. Bifunctional Photocatalysts for Enantioselective Aerobic Oxidation of β-Ketoesters

Ding, W.1; Lu, L.-Q.1; Zhou, Q.-Q.; Wei, Y.; Chen, J.-R.; Xiao, W.-J.*

J. Am. Chem. Soc., 2017, 139, 63-66.

DOI: 10.1021/jacs.6b11418

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