DOI: 10.1055/s-00000083

Synlett

Issue 20 · Volume 26 · December 2015 DOI: 10.1055/s-005-30567

synpacts

  • 2731
    Esguerra, Kenneth Virgel N.; Lumb, Jean-Philip:

    Adapting Melanogenesis to a Regioselective C–H Functionalization of Phenols

    Image for article: Adapting Melanogenesis to a Regioselective C–H Functionalization of Phenols
  • 2739
    Keohane, Colleen E.; Steele, Andrew D.; Wuest, William M.:

    The Rhizosphere Microbiome: A Playground for Natural Product Chemists

    Image for article: The Rhizosphere Microbiome: A Playground for Natural Product Chemists
  • 2745
    Li, Jundong; Zhao, Huaibo; Zhang, Yandong:

    Recent Progress in the Synthesis of 5-Unsubstituted Pyrrolidines via [3+2] Cycloadditions

    Image for article: Recent Progress in the Synthesis of 5-Unsubstituted Pyrrolidines via [3+2] Cycloadditions

    • account

  • 2751
    Sun, Huan; Huang, Yong:

    Recent Progress in the Development of Multitasking Directing Groups for Carbon–Hydrogen Activation Reactions

    Image for article: Recent Progress in the Development of Multitasking Directing Groups for Carbon–Hydrogen Activation Reactions
  • 2763
    Gauchot, Vincent; Gravel, Julien; Vidal, Marc; Charbonneau, Mathieu; Kairouz, Vanessa; Schmitzer, Andreea R.:

    Imidazolium and Benzimidazolium Salts: A Veritable Playground for Organic and Supramolecular Chemists

    Image for article: Imidazolium and Benzimidazolium Salts: A Veritable Playground for Organic and Supramolecular Chemists

    • cluster

  • 2780

    Cluster Cover Page

    Image for article: Cluster Cover Page
  • 2782
    Snieckus, Victor; Knochel, Paul:

    Cluster Preface: Resurgence of Synthetic Aromatic Chemistry

    Image for article: Cluster Preface: Resurgence of Synthetic Aromatic Chemistry
  • 2784
    Zhang, Zhan; Xu, Lijun; Chen, Zhengkai; Liu, Zhubo; Miao, Maozhong; Song, Jinyu; Ren, Hongjun:

    Nickel-Catalyzed Regioselective Reductive Cross-Coupling of Aryl Halides with Polysubstituted Allyl Halides in the Presence of Imidazolium Salts

    Image for article: Nickel-Catalyzed Regioselective Reductive Cross-Coupling of Aryl Halides with Polysubstituted Allyl Halides in the Presence of Imidazolium Salts
    Supporting Information (PDF)
  • 2789
    Martina, Katia; Rinaldi, Laura; Baricco, Francesca; Boffa, Luisa; Cravotto, Giancarlo:

    Highly Efficient Mechanochemical N-Arylation of Amino Alcohols and Diamines with Cu0 Powder

    Image for article: Highly Efficient Mechanochemical N-Arylation of Amino Alcohols and Diamines with Cu<sup>0</sup> Powder
    Supporting Information (PDF)
  • 2795
    dos Santos, Fernanda M.; Batista, João H. C.; Vessecchi, Ricardo; Clososki, Giuliano C.:

    Directed Functionalization of Cyano-Substituted Furans and Thiophenes with TMPMgCl·LiCl

    Image for article: Directed Functionalization of Cyano-Substituted Furans and Thiophenes with TMPMgCl·LiCl
    Supporting Information (PDF)
  • 2801
    Koga, Rintaro; Oishi, Tohru; Torikai, Kohei:

    Tuned Classical Thermal Aromatization Furnishing an Estrogenic Benzoacridine

    Image for article: Tuned Classical Thermal Aromatization Furnishing an Estrogenic Benzoacridine
    Supporting Information (PDF)
  • 2806
    Rasheed, Omer K.; Raftery, James; Quayle, Peter:

    A New Benzannulation Reaction of Azoaromatics

    Image for article: A New Benzannulation Reaction of Azoaromatics
    Supporting Information (PDF)
  • 2811
    Marquise, Nada; Nguyen, Tan Tai; Chevallier, Floris; Picot, Laurent; Thiéry, Valérie; Lozach, Olivier; Bach, Stéphane; Ruchaud, Sandrine; Mongin, Florence:

    Azine and Diazine Functionalization Using 2,2,6,6-Tetramethylpiperidino-Based Lithium–Metal Combinations: Application to the Synthesis of 5,9-Disubstituted Pyrido[3′,2′:4,5]pyrrolo[1,2-c]pyrimidines

    Image for article: Azine and Diazine Functionalization Using 2,2,6,6-Tetramethylpiperidino-Based Lithium–Metal Combinations: Application to the Synthesis of 5,9-Disubstituted Pyrido[3′,2′:4,5]pyrrolo[1,2-<i>c</i>]pyrimidines
    Supporting Information (PDF)
  • 2817
    Wu, Hao; Sheng, Wei-Jian; Chen, Bin; Liu, Ren-Rong; Gao, Jian-Rong; Jia, Yi-Xia:

    Nickel-Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with β,β-Disubstituted Nitroalkenes

    Image for article: Nickel-Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with β,β-Disubstituted Nitroalkenes
    Supporting Information (PDF)
  • 2821
    Zhang, Xiao-Yan; Hu, Li-Li; Shen, Ze; Chen, Zhong-Zhu; Xu, Zhi-Gang; Li, Shi-Qiang; Xie, Jian-Wu; Cui, Hai-Lei:

    Copper-Catalyzed Synthesis of Furo[3,2-c]coumarins and Dihydrofuro[3,2-c]coumarins through a Propargylation/Alkyne Oxacyclization/Isomerization Cascade under Microwave Irradiation

    Image for article: Copper-Catalyzed Synthesis of Furo[3,2-<i>c</i>]coumarins and Dihydrofuro[3,2-<i>c</i>]coumarins through a Propargylation/Alkyne Oxacyclization/Isomerization Cascade under Microwave Irradiation
    Supporting Information (PDF)
  • 2826
    Yang, De-Suo; Ke, Sen; Fan, Ming-Jin; Zhu, Hai-Tao; Wang, Xiao-Ling; Guan, Zheng-Hui:

    A Facile and Efficient Synthesis of Six-Membered Enol Carbocyclic Compounds

    Image for article: A Facile and Efficient Synthesis of Six-Membered Enol Carbocyclic Compounds
    Supporting Information (PDF)
  • 2831
    Chen, Jie; Xiong, Xiaoyu; Chen, Zenghua; Huang, Jianhui:

    Imidazolium Salt Catalyzed para-Selective Halogenation of Electron-Rich Arenes

    Image for article: Imidazolium Salt Catalyzed <i>para</i>-Selective Halogenation of Electron-Rich Arenes
    Supporting Information (PDF)

    • letter

  • 2835
    Nale, Deepak B.; Bhanage, Bhalchandra M.:

    N-Substituted Formamides as C1-Sources for the Synthesis of Benzimidazole and Benzothiazole Derivatives by Using Zinc Catalysts

    Image for article: N-Substituted Formamides as C<sub>1</sub>-Sources for the Synthesis of Benzimidazole and Benzothiazole Derivatives by Using Zinc Catalysts
    Supporting Information (PDF)
  • 2843
    Sun, Meng; Zhang, Liang; Hua, Cheng-Wen; Wang, Zhe; Hou, Le-Kai; Cai, Su-Xian; Li, Shuang:

    Palladium-Catalyzed Regioselective C–H Bond Acetoxylation–Alkoxylation of Azoxybenzenes

    Image for article: Palladium-Catalyzed Regioselective C–H Bond Acetoxylation–Alkoxylation of Azoxybenzenes
    Supporting Information (PDF)
  • 2849
    Liu, Zheng; Wang, Leifeng; Liu, Dong; Wang, Zhigang:

    Visible-Light-Mediated Oxidative Decarboxylative Coupling of Cinnamic Acid Derivatives with Tetrahydrofuran

    Image for article: Visible-Light-Mediated Oxidative Decarboxylative Coupling of Cinnamic Acid Derivatives with Tetrahydrofuran
    Supporting Information (PDF)
  • 2853
    Hu, Peng; Bach, Thorsten:

    Synthesis of Alkyl-Substituted Pyridines by Directed Pd(II)-Catalyzed C–H Activation of Alkanoic Amides

    Image for article: Synthesis of Alkyl-Substituted Pyridines by Directed Pd(II)-Catalyzed C–H Activation of Alkanoic Amides
    Supporting Information (PDF)
  • 2858
    Han, Xiaoyu; Wang, Yongjiang; Gai, Xikun; Zeng, Xiaofei:

    Highly Enantio- and Diastereoselective l-Proline Derived Acetylglucose Amide Catalyzed Aldol Reaction of Ketones to Aldehydes under Solvent-Free Conditions

    Image for article: Highly Enantio- and Diastereoselective <sc>l</sc>-Proline Derived Acetylglucose Amide Catalyzed Aldol Reaction of Ketones to Aldehydes under Solvent-Free Conditions
    Supporting Information (PDF)
  • 2863
    Li, Zheng; Li, Tianpeng; Li, Jiasheng; He, Lili; Jia, Xianggui; Yang, Jingya:

    2-Hydroxylation of 1,3-Diketones with Atmospheric Oxygen

    Image for article: 2-Hydroxylation of 1,3-Diketones with Atmospheric Oxygen
    Supporting Information (PDF)
  • 2866
    Hu, Ting; Yan, Hao; Liu, Xingxing; Wu, Chaoyang; Fan, Yuxing; Huang, Jing; Huang, Guosheng:

    Metal-Free sp3 C–H Functionalization: PABS/I2-Promoted Synthesis of Polysubstituted Oxazole Derivatives from Arylethanones and 2-Amino-2-alkyl/arylacetic Acid

    Image for article: Metal-Free sp<sup>3</sup> C–H Functionalization: PABS/I<sub>2</sub>-Promoted Synthesis of Polysubstituted Oxazole Derivatives from Arylethanones and 2-Amino-2-alkyl/arylacetic Acid
    Supporting Information (PDF)