Search Results - "Ji, Wangqin"

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  1. 1
    Sunlight-Driven Decarboxylative Alkynylation of α-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones

    Sunlight-Driven Decarboxylative Alkynylation of α-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones by Tan, Hui, Li, Hongji, Ji, Wangqin, Wang, Lei

    Published in Angewandte Chemie International Edition (13-07-2015)
    “…A novel and practical decarboxylative alkynylation of α‐keto acids with bromoacetylenes is catalyzed by hypervalent iodine(III) reagents when irradiation by…”
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  2. 2
    Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki–Miyaura Cross-coupling

    Axially Chiral Biaryl Monophosphine Oxides Enabled by Palladium/WJ-Phos-Catalyzed Asymmetric Suzuki–Miyaura Cross-coupling by Ji, Wangqin, Wu, Hai-Hong, Zhang, Junliang

    Published in ACS catalysis (17-01-2020)
    “…A highly enantioselective palladium/WJ-Phos-catalyzed Suzuki–Miyaura coupling reaction for efficient construction of axially chiral biaryl monophosphine oxides…”
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  3. 3
    Visible Light‐Induced Decarboxylative Acylarylation of Phenyl Propiolates with α‐Oxocarboxylic Acids to Coumarins Catalyzed by Hypervalent Iodine Reagents under Transition Metal‐Free Conditions

    Visible Light‐Induced Decarboxylative Acylarylation of Phenyl Propiolates with α‐Oxocarboxylic Acids to Coumarins Catalyzed by Hypervalent Iodine Reagents under Transition Metal‐Free Conditions by Yang, Shuai, Tan, Hui, Ji, Wangqin, Zhang, Xiangbiao, Li, Pinhua, Wang, Lei

    Published in Advanced synthesis & catalysis (02-02-2017)
    “…No…”
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  4. 4
    Sunlight-Driven Decarboxylative Alkynylation of [alpha]-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones

    Sunlight-Driven Decarboxylative Alkynylation of [alpha]-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones by Tan, Hui, Li, Hongji, Ji, Wangqin, Wang, Lei

    Published in Angewandte Chemie International Edition (13-07-2015)
    “…A novel and practical decarboxylative alkynylation of [alpha]-keto acids with bromoacetylenes is catalyzed by hypervalent iodine(III) reagents when irradiation…”
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  5. 5
    Visible Light-Induced Decarboxylative Acylarylation of Phenyl Propiolates with [alpha]-Oxocarboxylic Acids to Coumarins Catalyzed by Hypervalent Iodine Reagents under Transition Metal-Free Conditions

    Visible Light-Induced Decarboxylative Acylarylation of Phenyl Propiolates with [alpha]-Oxocarboxylic Acids to Coumarins Catalyzed by Hypervalent Iodine Reagents under Transition Metal-Free Conditions by Yang, Shuai, Tan, Hui, Ji, Wangqin, Zhang, Xiangbiao, Li, Pinhua, Wang, Lei

    Published in Advanced synthesis & catalysis (01-02-2017)
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  6. 6
    Sunlight-Driven Decarboxylative Alkynylation of α-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones

    Sunlight-Driven Decarboxylative Alkynylation of α-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones by Tan, Hui, Li, Hongji, Ji, Wangqin, Wang, Lei

    Published in Angewandte Chemie (13-07-2015)
    “…A novel and practical decarboxylative alkynylation of α‐keto acids with bromoacetylenes is catalyzed by hypervalent iodine(III) reagents when irradiation by…”
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  7. 7
    Sunlight-Driven Decarboxylative Alkynylation of [alpha]-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones

    Sunlight-Driven Decarboxylative Alkynylation of [alpha]-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones by Tan, Hui, Li, Hongji, Ji, Wangqin, Wang, Lei

    Published in Angewandte Chemie (13-07-2015)
    “…A novel and practical decarboxylative alkynylation of [alpha]-keto acids with bromoacetylenes is catalyzed by hypervalent iodine(III) reagents when irradiation…”
    Get full text
    Journal Article
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