DOI: 10.1055/s-00000083

Synlett

Issue Editorial Board · Volume · 2021 DOI: 10.1055/s-011-51992

Editorial Board Collection

  • Purta, Anggi Eka; Ichii, Shun; Tazawa, Aya; Uozumi, Yasuhiro:

    C−H Arylation of Thiophenes with Aryl Bromides by a Parts-per-Million Loading of a Palladium NNC-Pincer Complex

    Image for article: C−H Arylation of Thiophenes with Aryl Bromides by a Parts-per-Million Loading of a Palladium NNC-Pincer Complex
    Supporting Information (PDF)
  • Chang, Chu-An; Gürtzgen, Stefan; Johnson, Erik P.; Vollhardt, K. Peter C.:

    Stoichiometric and Catalytic (η5-Cyclopentadienyl)cobalt-Mediated Cycloisomerizations of Ene-Yne-Ene Type Allyl Propargyl Ethers

    Image for article: Stoichiometric and Catalytic (<i>η</i><sup>5</sup>-Cyclopentadienyl)cobalt-Mediated Cycloisomerizations of Ene-Yne-Ene Type Allyl Propargyl Ethers
    Supporting Information (PDF)
  • O’Brien, Connor J.; Nicewicz, David A.:

    Milled Dry Ice as a C1 Source for the Carboxylation of Aryl Halides

    Image for article: Milled Dry Ice as a C1 Source for the Carboxylation of Aryl Halides
    Supporting Information (PDF)
  • van Gemmeren, Manuel; List, Benjamin:

    How and Why Crowd Reviewing Works

    Image for article: How and Why Crowd Reviewing Works
    Open Access
  • Martin, Ruben; Molander, Gary A.:

    Cluster Preface: Modern Nickel-Catalyzed Reactions

    Image for article: Cluster Preface: Modern Nickel-Catalyzed Reactions
  • Osako, Takao; Srisa, Jakkrit; Torii, Kaoru; Hamasaka, Go; Uozumi, Yasuhiro:

    Iterative Preparation of Platinum Nanoparticles in an Amphiphilic Polymer Matrix: Regulation of Catalytic Activity in Hydrogenation

    Image for article: Iterative Preparation of Platinum Nanoparticles in an Amphiphilic Polymer Matrix: Regulation of Catalytic Activity in Hydrogenation
    Supporting Information (PDF)
  • Uttry, Alexander; van Gemmeren, Manuel:

    Direct C(sp3)–H Activation of Carboxylic Acids

    Image for article: Direct C(sp<sup>3</sup>)–H Activation of Carboxylic Acids
  • Santiago, Carlos; Chen, Hao; Mondal, Arup; van Gemmeren, Manuel:

    Dual Ligand-Enabled Late-Stage Fujiwara–Moritani Reactions

    Image for article: Dual Ligand-Enabled Late-Stage Fujiwara–Moritani Reactions
    Supporting Information (PDF)
  • Colovray-Gotteland, Véronique; Harvey, Daniel F.; Johnson, Barry M.; Ung, Christopher S.; Vollhardt, K. Peter C.:

    Inter- and Intramolecular [2+2+2] Cycloaddition of Alkyne Triple Bonds to the Carbonyl Function of Aldehydes and Ketones Enabled by η5-Cyclopentadienylcobalt(L)(L′)

    Image for article: Inter- and Intramolecular [2+2+2] Cycloaddition of Alkyne Triple Bonds to the Carbonyl Function of Aldehydes and Ketones Enabled by η<sup>5</sup>-Cyclopentadienylcobalt(L)(L′)
    Supporting Information (PDF)
  • Lee, Sumin; Jang, Young Jin; Phipps, Erik J. T.; Lei, Honghui; Rovis, Tomislav:

    Rhodium(III)-Catalyzed Three-Component 1,2-Diamination of Unactivated Terminal Alkenes

    Image for article: Rhodium(III)-Catalyzed Three-Component 1,2-Diamination of Unactivated Terminal Alkenes
    Supporting Information (PDF)
  • Campeau, Louis-Charles; Rovis, Tomislav:

    Preface: Modern Heterocycle Synthesis and Functionalization

    Image for article: Preface: Modern Heterocycle Synthesis and Functionalization
  • Higginson, Bradley; Sanjosé-Orduna, Jesus; Gu, Yiting; Martin, Ruben:

    Nickel-Catalyzed Photodehalogenation of Aryl Bromides

    Image for article: Nickel-Catalyzed Photodehalogenation of Aryl Bromides
    Supporting Information (PDF)
  • Onuska, Nicholas P. R.; Schutzbach-Horton, Megan E.; Rosario Collazo, José L.; Nicewicz, David. A.:

    Anti-Markovnikov Hydroazidation of Activated Olefins via Organic Photoredox Catalysis

    Image for article: Anti-Markovnikov Hydroazidation of Activated Olefins via Organic Photoredox Catalysis
    Supporting Information (PDF)
  • Kang, Yi Cheng; Treacy, Sean M.; Rovis, Tomislav:

    Iron-Catalyzed C(sp3)–H Alkylation through Ligand-to-Metal Charge Transfer

    Image for article: Iron-Catalyzed C(sp<sup>3</sup>)–H Alkylation through Ligand-to-Metal Charge Transfer
    Supporting Information (PDF)
  • Dahlmann, Uwe; Vollhardt, K. Peter C.:

    Oligoether-Substituted Derivatives of Carbon-Rich 1,4,7,10,13,16-Hexaethynyltribenzo[a,e,i]cyclododeca-5,11,17-triyne (C36H12) and 1,4,9,12-Tetrakis(ethynyl)dibenzo[a,g]cyclododeca-5,7,13,15-tetrayne (C28H8): Potential Precursors to the Circular [6]Phenylene (‘Antikekulene’) Frame

    Image for article: Oligoether-Substituted Derivatives of Carbon-Rich 1,4,7,10,13,16-Hexaethynyltribenzo[<i>a</i>,<i>e</i>,<i>i</i>]cyclododeca-5,11,17-triyne (C<sub>36</sub>H<sub>12</sub>) and 1,4,9,12-Tetrakis(ethynyl)dibenzo[<i>a</i>,<i>g</i>]cyclododeca-5,7,13,15-tetrayne (C<sub>28</sub>H<sub>8</sub>): Potential Precursors to the Circular [6]Phenylene (‘Antikekulene’) Frame
    Supporting Information (PDF)
  • Wong, Jonathan J.; Chen, Xiangyang; Houk, Kendall N.; Vollhardt, K. Peter C.:

    The Trajectory of the (η5-Cyclopentadienyl)cobalt-Mediated Cycloisomerization of Ene-Yne-Ene-Type Allyl Propargylic Ethers to Furans: A DFT Appraisal

    Image for article: The Trajectory of the (<i>η</i><sup>5</sup>-Cyclopentadienyl)cobalt-Mediated Cycloisomerization of Ene-Yne-Ene-Type Allyl Propargylic Ethers to Furans: A DFT Appraisal
    Supporting Information (PDF) xyz File (OTHER)
  • Zhou, Hui; Zhang, Pinglu; List, Benjamin:

    The Silicon–Hydrogen Exchange Reaction: Catalytic Kinetic Resolution of 2-Substituted Cyclic Ketones

    Image for article: The Silicon–Hydrogen Exchange Reaction: Catalytic Kinetic Resolution of 2-Substituted Cyclic Ketones
    Open Access
    Supporting Information (PDF)
  • Zhang, Zhipeng; Klussmann, Martin; List, Benjamin:

    Kinetic Study of Disulfonimide-Catalyzed Cyanosilylation of Aldehydes by Using a Method of Progress Rates

    Image for article: Kinetic Study of Disulfonimide-Catalyzed Cyanosilylation of Aldehydes by Using a Method of Progress Rates
    Supporting Information (PDF)
  • Wakchaure, Vijay N.; Obradors, Carla; List, Benjamin:

    Chiral Brønsted Acids Catalyze Asymmetric Additions to Substrates that Are Already Protonated: Highly Enantioselective Disulfonimide-Catalyzed Hantzsch Ester Reductions of NH–Imine Hydrochloride Salts

    Image for article: Chiral Brønsted Acids Catalyze Asymmetric Additions to Substrates that Are Already Protonated: Highly Enantioselective Disulfonimide-Catalyzed Hantzsch Ester Reductions of NH–Imine Hydrochloride Salts
    Supporting Information (PDF)