DOI: 10.1055/s-00000084

Synthesis

Ausgabe 06 · Volume 52 · März 2020 DOI: 10.1055/s-010-46047

table of contents

  • V

    Linked PDF of Table of Contents

    • review

  • 781
    Reznikov, Alexander N.; Klimochkin, Yuri N.:

    Recent Developments in Highly Stereoselective Michael Addition Reactions Catalyzed by Metal Complexes

    Image for article: Recent Developments in Highly Stereoselective Michael Addition Reactions Catalyzed by Metal Complexes

    • short review

  • 796
    Song, Si-Zhe; Dong, Youren; Ge, Guo-Ping; Li, Qiang; Wei, Wen-Ting:

    Recent Advances in Radical Nitration Using tert-Butyl Nitrite

    Image for article: Recent Advances in Radical Nitration Using <i>tert</i>-Butyl Nitrite
  • 807
    Youn, So Won:

    Transition-Metal-Catalyzed Annulative Coupling Cascade for the Synthesis of 3-Methyleneisoindolin-1-ones

    Image for article: Transition-Metal-Catalyzed Annulative Coupling Cascade for the Synthesis of 3-Methyleneisoindolin-1-ones
  • 819
    Hsieh, Jen-Chieh; Su, Haw-Lih:

    Synthesis of N-Heterocycles via Transition-Metal-Catalyzed Tandem Addition/Cyclization of a Nitrile

    Image for article: Synthesis of <i>N</i>-Heterocycles via Transition-Metal-Catalyzed Tandem Addition/Cyclization of a Nitrile

    • feature

  • 834
    Gao, Qianwen; Liu, Ze-Shui; Hua, Yu; Zhou, Siwei; Cheng, Hong-Gang; Zhou, Qianghui:

    Alkyl Tosylates as Alkylating Reagents in the Catellani Reaction

    Image for article: Alkyl Tosylates as Alkylating Reagents in the Catellani Reaction
    Supporting Information (PDF)

    • psp

  • 847
    Morra, Barbora; Morra, Nicholas A.; MacDonald, Daniel G.; Pagenkopf, Brian L.:

    Gram-Scale Synthesis of the Co(nmp)2 Catalyst to Prepare trans-2,5-Disubstituted Tetrahydrofurans by the Aerobic Oxidative Cyclization of Pent-4-en-1-ols

    Image for article: Gram-Scale Synthesis of the Co(nmp)<sub>2</sub> Catalyst to Prepare <i>trans</i>-2,5-Disubstituted Tetrahydrofurans by the Aerobic Oxidative Cyclization of Pent-4-en-1-ols
    Supporting Information (PDF) CIF File (OTHER)

    • paper

  • 853
    Kohlhaas, Martha; Lutz, Fabian; Paransothy, Nirtharsan; Octa-Smolin, Frescilia; Wölper, Christoph; Niemeyer, Jochen:

    Synthesis of Bis-BINOL Derivatives: Linking via the 3-, 4-, or 5-Position by Generation of Suitable C1-Symmetric Precursors

    Image for article: Synthesis of Bis-BINOL Derivatives: Linking via the 3-, 4-, or 5-Position by Generation of Suitable <i>C</i><sub>1</sub>-Symmetric Precursors
    Supporting Information (PDF) CIF File (OTHER)
  • 861
    Chang, Meng-Yang; Chen, Kuan-Ting; Tsai, Yu-Lin; Chen, Han-Yu:

    One-Pot Access to 2-Aryl-3-(arylmethyl)chromones

    Image for article: One-Pot Access to 2-Aryl-3-(arylmethyl)chromones
    Supporting Information (PDF)
  • 873
    Skotnitzki, Juri; Kremsmair, Alexander; Kicin, Bilal; Saeb, Rakan; Ruf, Vincent; Knochel, Paul:

    Stereoselective anti-SN2′-Substitutions of Secondary Alkylcopper-Zinc Reagents with Allylic Epoxides: Total Synthesis of (3S,6R,7S)-Zingiberenol

    Image for article: Stereoselective <i>anti</i>-S<sub>N</sub>2′-Substitutions of Secondary Alkylcopper-Zinc Reagents with Allylic Epoxides: Total Synthesis of (3<i>S</i>,6<i>R</i>,7<i>S</i>)-Zingiberenol
    Supporting Information (PDF)
  • 882
    Pruschinski, Lucas; Lücke, Ana-Luiza; Freese, Tyll; Kahnert, Sean-Ray; Mummel, Sebastian; Schmidt, Andreas:

    Suzuki–Miyaura Cross-Couplings under Acidic Conditions

    Image for article: Suzuki–Miyaura Cross-Couplings under Acidic Conditions
    Supporting Information (PDF)
  • 893
    Lu, Hai-Long; Guo, Fu-Hu; Wang, Tong-Lin; Wang, Xi-Cun; Quan, Zheng-Jun:

    Palladium-Catalyzed/Copper-Mediated Desulfurization and Aryl­­ation of Quinoline-2-(1H)-thione for Rapid Access to Quinoline Derivatives

    Image for article: Palladium-Catalyzed/Copper-Mediated Desulfurization and Aryl­­ation of Quinoline-2-(1<i>H</i>)-thione for Rapid Access to Quinoline Derivatives
    Supporting Information (PDF)
  • 901
    Liu, Yue; Zhang, Cheng; Liang, Xiaoxia; Zeng, Xianzhong; Lu, Rongmei; Fang, Zixuan; Wang, Shaoyu; Liu, Yanjun; Hu, Jinxing:

    Synthesis of 2-Imidazolines via Palladium-Catalyzed Cyclization Reaction of 2,3-Allenyl Amines and Aryl Iodides

    Image for article: Synthesis of 2-Imidazolines via Palladium-Catalyzed Cyclization Reaction of 2,3-Allenyl Amines and Aryl Iodides
    Supporting Information (PDF)
  • 909
    Dziuba, Kamil; Lubańska, Małgorzata; Pietrusiewicz, K. Michał:

    Enantiodivergent Synthesis of Both PAMPO Enantiomers Using l-Menthyl Chloroacetate and Stereomutation at P in Classical Quaternisation Reactions

    Image for article: Enantiodivergent Synthesis of Both PAMPO Enantiomers Using <sc>l</sc>-Menthyl Chloroacetate and Stereomutation at P in Classical Quaternisation Reactions
    Supporting Information (PDF)
  • 917
    Ban, Jaeyoung; Lim, Minkyung; Shabbir, Saira; Baek, Junghyun; Rhee, Hakjune:

    Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination

    Image for article: Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination
    Supporting Information (PDF)
  • 928
    Li, Yang; Guo, Hao; Fan, Renhua:

    Iodobenzene-Catalyzed Oxidative Cyclization for the Synthesis of Highly Functionalized Cyclopropanes

    Image for article: Iodobenzene-Catalyzed Oxidative Cyclization for the Synthesis of Highly Functionalized Cyclopropanes
    Supporting Information (PDF)
  • 933
    Bartolotta, Roberta; La Rosa, Concetta; Nava, Donatella:

    New Strategy of Synthesis of Peramivir Analogues as Potential Neuraminidase Inhibitors

    Image for article: New Strategy of Synthesis of Peramivir Analogues as Potential Neuraminidase Inhibitors
    Supporting Information (PDF)
  • 942
    Ohsawa, Kosuke; Zhao, Hongbin; Tokunaga, Takuya; Thomas, Carys; Ganesan, A.; Masuda, Yuichi; Doi, Takayuki:

    Stereoselective Synthesis of Protected l-allo-Enduracididine and l-Enduracididine via Asymmetric Nitroaldol Reaction

    Image for article: Stereoselective Synthesis of Protected <sc>l</sc>-<i>allo</i>-Enduracididine and <sc>l</sc>-Enduracididine via Asymmetric Nitroaldol Reaction
    Supporting Information (PDF)