DOI: 10.1055/s-00000083

Synlett

Ausgabe 19 · Volume 35 · Dezember 2024 DOI: 10.1055/s-014-60565

table of contents

  • V

    Linked PDF of Table of Contents

    • Synform

  • A182
    Zanda, Matteo:

    SYNFORM ISSUE 2024/12

    • cluster

    Isotopic Labeling

  • 2153
    van Gemmeren, Manuel; Beller, Matthias:

    Late-Stage C–H Deuteration of Organic Compounds via Ligand-Enabled Palladium-Catalyzed Hydrogen Isotope Exchange

    Image for article: Late-Stage C–H Deuteration of Organic Compounds via Ligand-Enabled Palladium-Catalyzed Hydrogen Isotope Exchange

    • account

    Isotopic Labeling

  • 2155
    Sib, Anna; Derdau, Volker:

    Method Development and Syntheses Examples of Isotopically Labeled Compounds to Foster Operational Excellence in Pharma Industry

    Image for article: Method Development and Syntheses Examples of Isotopically Labeled Compounds to Foster Operational Excellence in Pharma Industry
  • 2174
    Xiao, Siyu; Conte, Antonio; Cornelissen, Bart T.; Domling, Alexander; Elsinga, Philip H.:

    Multicomponent Reactions: A Promising Approach to Isotope Labeling

    Image for article: Multicomponent Reactions: A Promising Approach to Isotope Labeling
    Open Access
  • 2191
    Dey, Jyotirmoy; van Gemmeren, Manuel:

    Late-Stage C–H Deuteration of Organic Compounds via Ligand-Enabled Palladium-Catalyzed Hydrogen Isotope Exchange

    Image for article: Late-Stage C–H Deuteration of Organic Compounds via Ligand-Enabled Palladium-Catalyzed Hydrogen Isotope Exchange
    Open Access

    • letter

    Isotopic Labeling

  • 2201
    Mudd, Richard J.; Reid, Marc; Paterson, Laura C.; Atzrodt, Jens; Derdau, Volker; Kerr, William J.:

    Directing Hydrogen Isotope Exchange with Aryl Carboxylic Acids

    Image for article: Directing Hydrogen Isotope Exchange with Aryl Carboxylic Acids
    Supporting Information (PDF)
  • 2207
    Battisti, Umberto M.; Müller, Marius; García-Vázquez, Rocío; Herth, Matthias Manfred:

    Labeling of Highly Reactive Tetrazines using [18F]SuFEx

    Image for article: Labeling of Highly Reactive Tetrazines using [<sup>18</sup>F]SuFEx
    Supporting Information (PDF)
  • 2212
    Steverlynck, Joost; Sitdikov, Ruzal; Nikolaienko, Pavlo; Kale, Ajit Prabhakar; Rueping, Magnus:

    Trideuteromethylation of Alkyl and Aryl Bromides by Nickel-Catalyzed Electrochemical Reductive Cross-Electrophile Coupling

    Image for article: Trideuteromethylation of Alkyl and Aryl Bromides by Nickel-Catalyzed Electrochemical Reductive Cross-Electrophile Coupling
    Supporting Information (PDF)

    • account

  • 2217
    Sasamori, Takahiro:

    Small-Molecule Activation by Low-Coordinated Germanium Compounds

    Image for article: Small-Molecule Activation by Low-Coordinated Germanium Compounds

    • synpacts

  • 2229
    Lou, Xiangyu; Lin, Jiaxin; Lyu, Hairong:

    Stereoselective Synthesis of Unsymmetrical 1,1-Diborylalkenes

    Image for article: Stereoselective Synthesis of Unsymmetrical 1,1-Diborylalkenes

    • letter

  • 2236
    Xu, Xiao-Bo; Hao, Li-Qiang; Liu, Xian; Wang, Yang-Yang; Yang, Zhao-Zi-Yuan; Yu, Xiao; Ding, Dong; Ji, Ya-Fei:

    Synthesis of Fused-Ring Pyrrolizine Derivatives via a Copper-Catalyzed Radical Cascade Cyclization

    Image for article: Synthesis of Fused-Ring Pyrrolizine Derivatives via a Copper-Catalyzed Radical Cascade Cyclization
    Supporting Information (PDF)
  • 2241
    Li, Zhi-Bo; Zhang, Jin; Shi, Yi-Ran; Li, Hong; Yang, Min-Ge; Zhu, Wen-Qing; Fan, Qiang-Wei; Li, Yang:

    AgSCF3 Radical Addition Based on an Oxidant-Free α,β-Amide (Trifluoromethyl)sulfanylation Reaction

    Image for article: AgSCF<sub>3</sub> Radical Addition Based on an Oxidant-Free α,β-Amide (Trifluoromethyl)sulfanylation Reaction
    Supporting Information (PDF)
  • 2246
    Hu, Meng-Xue; Chen, Peng; Miao, Le-Wei; Shi, Jianghuan; Jiang, Yi-Jun:

    Iron(III) Triflate and γ-Cyclodextrin-Catalyzed Hydroarylation of Alkenes with 1-Naphthols and 2-Naphthols

    Image for article: Iron(III) Triflate and γ-Cyclodextrin-Catalyzed Hydroarylation of Alkenes with 1-Naphthols and 2-Naphthols
    Supporting Information (PDF)