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Fu-Peng Wu

Showing results (11-20 of 28) with videos related to

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Angewandte Chemie (International Ed. in English)|May 30, 2020
Four-Component Borocarbonylation of Vinylarenes Enabled by Cooperative Cu/Pd Catalysis: Access to β-Boryl Ketones and β-Boryl Vinyl EstersYang Yuan, Fu-Peng Wu, Jian-Xing Xu, et al.
The Journal of Organic Chemistry|August 19, 2017
Palladium-Catalyzed Carbonylative Transformation of Organic Halides with Formic Acid as the Coupling Partner and CO Source: Synthesis of Carboxylic AcidsFu-Peng Wu, Jin-Bao Peng, Xinxin Qi, et al.
Organic Letters|July 12, 2019
Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-ArylbutanalsFu-Peng Wu, Da Li, Jin-Bao Peng, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 8, 2019
Palladium-Catalyzed Tunable Carbonylative Synthesis of Enones and BenzofulvenesJin-Bao Peng, Fu-Peng Wu, Anke Spannenberg, et al.
Chemical Science|March 6, 2023
Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenesFu-Peng Wu, Xing-Wei Gu, Hui-Qing Geng, et al.
Journal of the American Chemical Society|August 14, 2020
Copper-Catalyzed Synthesis of Stereodefined Cyclopropyl Bis(boronates) from Alkenes with CO as the C1 SourceFu-Peng Wu, Xiaoling Luo, Udo Radius, et al.
Organic Letters|September 19, 2017
Direct Palladium-Catalyzed Carbonylative Transformation of Allylic Alcohols and Related DerivativesFu-Peng Wu, Jin-Bao Peng, Lu-Yang Fu, et al.
Angewandte Chemie (International Ed. in English)|March 27, 2020
Copper-Catalyzed Regioselective Borocarbonylative Coupling of Unactivated Alkenes with Alkyl Halides: Synthesis of β-Boryl KetonesFu-Peng Wu, Yang Yuan, Claas Schünemann, et al.
Iscience|October 16, 2018
Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl IodidesJin-Bao Peng, Fu-Peng Wu, Cong Xu, et al.
The Journal of Organic Chemistry|May 26, 2018
Nickel-Catalyzed Molybdenum-Promoted Carbonylative Synthesis of BenzophenonesJin-Bao Peng, Fu-Peng Wu, Da Li, et al.
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Showing results (11-20 of 28) with videos related to

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Pageof 3
Angewandte Chemie (International Ed. in English)|May 30, 2020
Four-Component Borocarbonylation of Vinylarenes Enabled by Cooperative Cu/Pd Catalysis: Access to β-Boryl Ketones and β-Boryl Vinyl EstersYang Yuan, Fu-Peng Wu, Jian-Xing Xu, et al.
The Journal of Organic Chemistry|August 19, 2017
Palladium-Catalyzed Carbonylative Transformation of Organic Halides with Formic Acid as the Coupling Partner and CO Source: Synthesis of Carboxylic AcidsFu-Peng Wu, Jin-Bao Peng, Xinxin Qi, et al.
Organic Letters|July 12, 2019
Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-ArylbutanalsFu-Peng Wu, Da Li, Jin-Bao Peng, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 8, 2019
Palladium-Catalyzed Tunable Carbonylative Synthesis of Enones and BenzofulvenesJin-Bao Peng, Fu-Peng Wu, Anke Spannenberg, et al.
Chemical Science|March 6, 2023
Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenesFu-Peng Wu, Xing-Wei Gu, Hui-Qing Geng, et al.
Journal of the American Chemical Society|August 14, 2020
Copper-Catalyzed Synthesis of Stereodefined Cyclopropyl Bis(boronates) from Alkenes with CO as the C1 SourceFu-Peng Wu, Xiaoling Luo, Udo Radius, et al.
Organic Letters|September 19, 2017
Direct Palladium-Catalyzed Carbonylative Transformation of Allylic Alcohols and Related DerivativesFu-Peng Wu, Jin-Bao Peng, Lu-Yang Fu, et al.
Angewandte Chemie (International Ed. in English)|March 27, 2020
Copper-Catalyzed Regioselective Borocarbonylative Coupling of Unactivated Alkenes with Alkyl Halides: Synthesis of β-Boryl KetonesFu-Peng Wu, Yang Yuan, Claas Schünemann, et al.
Iscience|October 16, 2018
Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl IodidesJin-Bao Peng, Fu-Peng Wu, Cong Xu, et al.
The Journal of Organic Chemistry|May 26, 2018
Nickel-Catalyzed Molybdenum-Promoted Carbonylative Synthesis of BenzophenonesJin-Bao Peng, Fu-Peng Wu, Da Li, et al.
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