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CF3SO2Na as a Bifunctional Reagent: Electrochemical Trifluoromethylation of Alkenes Accompanied by SO2 Insertion to Access Trifluoromethylated Cyclic N‐Sulfonylimines
CF3SO2Na as a Bifunctional Reagent: Electrochemical Trifluoromethylation of Alkenes Accompanied by SO2 Insertion to Access Trifluoromethylated Cyclic N‐Sulfonylimines
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CF3SO2Na as a Bifunctional Reagent: Electrochemical Trifluoromethylation of Alkenes Accompanied by SO2 Insertion to Access Trifluoromethylated Cyclic N‐Sulfonylimines

Li, Zheng ; Jiao, Lingcong ; Sun, Yunhai ; He, Zeying ; Wei, Zhonglin ; Liao, Wei‐Wei

Angewandte Chemie International Edition, 2020-04, Vol.59 (18), p.7266-7270 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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2
Organocatalytic Allylic Alkylation of α‑(Alkylideneamino)nitriles and Its Application in the Preparation of Multisubstituted 1‑Pyrrolines
Organocatalytic Allylic Alkylation of α‑(Alkylideneamino)nitriles and Its Application in the Preparation of Multisubstituted 1‑Pyrrolines
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Organocatalytic Allylic Alkylation of α‑(Alkylideneamino)nitriles and Its Application in the Preparation of Multisubstituted 1‑Pyrrolines

Zhao, Lang ; Yan, Yan ; Wei, Zhong-Lin ; Liao, Wei-Wei

Journal of organic chemistry, 2022-08, Vol.87 (15), p.10090-10104 [Periódico revisado por pares]

American Chemical Society

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3
Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences
Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences
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Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences

Wang, Ting-Ting ; Zhang, Di ; Liao, Wei-Wei

Chemical communications (Cambridge, England), 2018, Vol.54 (16), p.2048-2051 [Periódico revisado por pares]

England: Royal Society of Chemistry

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4
Electrochemical Trifluoromethylation/Bicyclization of N‑Cyanamide Alkenes: Synthesis of Bicyclic Amidine Derivatives
Electrochemical Trifluoromethylation/Bicyclization of N‑Cyanamide Alkenes: Synthesis of Bicyclic Amidine Derivatives
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Electrochemical Trifluoromethylation/Bicyclization of N‑Cyanamide Alkenes: Synthesis of Bicyclic Amidine Derivatives

Yan, Zhi-Hua ; Yan, Yan ; Wei, Zhong-Lin ; Liao, Wei-Wei

Journal of organic chemistry, 2024-02, Vol.89 (4), p.2718-2725 [Periódico revisado por pares]

United States: American Chemical Society

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5
Diastereo- and Enantioselective Synthesis of Functionalized Dihydropyrans via an Organocatalytic Claisen Rearrangement/Oxa-Michael Addition Tandem Sequence
Diastereo- and Enantioselective Synthesis of Functionalized Dihydropyrans via an Organocatalytic Claisen Rearrangement/Oxa-Michael Addition Tandem Sequence
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Diastereo- and Enantioselective Synthesis of Functionalized Dihydropyrans via an Organocatalytic Claisen Rearrangement/Oxa-Michael Addition Tandem Sequence

Li, Wen-Cheng ; Yang, Lei ; Wei, Zhong-Lin ; Liao, Wei-Wei

Organic letters, 2023-09, Vol.25 (34), p.6434-6439 [Periódico revisado por pares]

American Chemical Society

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6
Highly diastereo- and enantioselective construction of phthalide-oxindole hybrids bearing vicinal quaternary chiral centers via an organocatalytic allylic alkylation
Highly diastereo- and enantioselective construction of phthalide-oxindole hybrids bearing vicinal quaternary chiral centers via an organocatalytic allylic alkylation
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Highly diastereo- and enantioselective construction of phthalide-oxindole hybrids bearing vicinal quaternary chiral centers via an organocatalytic allylic alkylation

Liu, Wei ; Hu, Zhi-Peng ; Yan, Yan ; Liao, Wei-Wei

Tetrahedron letters, 2018-08, Vol.59 (32), p.3132-3135 [Periódico revisado por pares]

Elsevier Ltd

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7
An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins
An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins
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An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins

Sun, Zhen ; Li, Zheng ; Liao, Wei-Wei

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (7), p.1614-1618 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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8
Synthesis of 2,4,5-Trisubstituted Oxazoles via Pd-Catalyzed C–H Addition to Nitriles/Cyclization Sequences
Synthesis of 2,4,5-Trisubstituted Oxazoles via Pd-Catalyzed C–H Addition to Nitriles/Cyclization Sequences
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Synthesis of 2,4,5-Trisubstituted Oxazoles via Pd-Catalyzed C–H Addition to Nitriles/Cyclization Sequences

Zhang, Di ; Song, Hao ; Cheng, Na ; Liao, Wei-Wei

Organic letters, 2019-04, Vol.21 (8), p.2745-2749 [Periódico revisado por pares]

United States: American Chemical Society

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9
Multicomponent Cyclization with an Inorganic Sulfur Dioxide Surrogate: Straightforward Construction of Difluorinated Benzosultams
Multicomponent Cyclization with an Inorganic Sulfur Dioxide Surrogate: Straightforward Construction of Difluorinated Benzosultams
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Multicomponent Cyclization with an Inorganic Sulfur Dioxide Surrogate: Straightforward Construction of Difluorinated Benzosultams

Wu, Yu-Heng ; Li, Cheng-Jing ; Wei, Zhong-Lin ; Liao, Wei-Wei

Organic letters, 2022-12, Vol.24 (49), p.9112-9117 [Periódico revisado por pares]

United States: American Chemical Society

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10
Electrochemical tandem cyclization to access sulfonylated fused sultams via SO2 insertion with sodium metabisulfite
Electrochemical tandem cyclization to access sulfonylated fused sultams via SO2 insertion with sodium metabisulfite
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Electrochemical tandem cyclization to access sulfonylated fused sultams via SO2 insertion with sodium metabisulfite

Yun-Hai, Sun ; Cheng-Jing, Li ; Ji-Ming, Xi ; Zhong-Lin, Wei ; Wei-Wei, Liao

Organic chemistry frontiers an international journal of organic chemistry, 2023-01, Vol.10 (3), p.705-711 [Periódico revisado por pares]

London: Royal Society of Chemistry

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