DOI: 10.1055/s-00000084

Synthesis

Issue 19 · Volume 2008 · October 2008 DOI: 10.1055/s-002-13137

synform

  • A93
    Zanda, Matteo:

    SYNFORM ISSUE 2008/09

    • review

  • 3013
    Kakiuchi, Fumitoshi; Kochi, Takuya:

    Transition-Metal-Catalyzed Carbon-Carbon Bond Formation via Carbon-Hydrogen Bond Cleavage

    Image for article: Transition-Metal-Catalyzed Carbon-Carbon Bond Formation via Carbon-Hydrogen Bond Cleavage

    • short paper

  • 3040
    Balogh, János; Mahó, Sándor; Háda, Viktor; Kollár, László; Skoda-Földes, Rita:

    Facile Synthesis of Steroidal Primary Amides via Palladium-Catalyzed Aminocarbonylation of Steroidal Alkenyl Halides

    Image for article: Facile Synthesis of Steroidal Primary Amides via Palladium-Catalyzed Aminocarbonylation of Steroidal Alkenyl Halides

    • paper

  • 3043
    Peng, Fangzhi; Fan, Baomin; Shao, Zhihui; Pu, Xuewei; Li, Penghui; Zhang, Hongbin:

    Cu(OTf)2-Catalyzed Isomerization of 7-Oxabicyclic Alkenes: A Practical Route to the Synthesis of 1-Naphthol Derivatives

    Image for article: Cu(OTf)<SUB>2</SUB>-Catalyzed Isomerization of 7-Oxabicyclic Alkenes: A Practical Route to the Synthesis of 1-Naphthol Derivatives
  • 3047
    Prukała, Wiesław; Majchrzak, Mariusz; Posała, Krystian; Marciniec, Bogdan:

    A Convenient One-Pot Synthesis of Bis[(E)-4-halostyryl]arene Derivatives

    Image for article: A Convenient One-Pot Synthesis of Bis[(<EM EMTYPE="ITALIC">E</EM>)-4-halostyryl]arene Derivatives
  • 3053
    Madre, Marina; Petrova, Marina; Belyakov, Sergey:

    The Determinative Influence of the O6-(Diphenylcarbamoyl) Group on the Exocyclic Nitrogen Benzylation in 2-Amino-6-oxopurine Derivatives

    Image for article: The Determinative Influence of the O<SUP>6</SUP>-(Diphenylcarbamoyl) Group on the Exocyclic Nitrogen Benzylation in 2-Amino-6-oxopurine Derivatives
  • 3061
    Bhaskar, Gopishetti; Kumar, Anchoori Ravi; Ramu, Errabelli; Rao, Batchu Venkateswara:

    Synthesis of a Hydroxyethylene Dipeptide Isostere, a Core Unit of the HIV Protease Inhibitors Ritonavir and Lopinavir, and Its C-5 Epimer

    Image for article: Synthesis of a Hydroxyethylene Dipeptide Isostere, a Core Unit of the HIV Protease Inhibitors Ritonavir and Lopinavir, and Its C-5 Epimer
  • 3065
    Senn-Bilfinger, Jörg; Kohl, Bernhard; Rainer, Georg; Buhr, Wilm; Holst, Hans Christof; Zimmermann, Peter Jan:

    Synthesis of Substituted Imidazo[1,2-h][1,7]naphthyridines as H+/K+-ATPase Inhibiting Drug Precursors via Directed ortho-Metalation of Imidazo[1,2-a]pyridines

    Image for article: Synthesis of Substituted Imidazo[1,2-<EM EMTYPE="ITALIC">h</EM>][1,7]naphthyridines as H<SUP>+</SUP>/K<SUP>+</SUP>-ATPase Inhibiting Drug Precursors via Directed <EM EMTYPE="ITALIC">ortho</EM>-Metalation of Imidazo[1,2-<EM EMTYPE="ITALIC">a</EM>]pyridines
  • 3071
    Buehrdel, Gunther; Beckert, Rainer; Petrlikova, Eva; Herzigova, Petra; Klimesova, Vera; Fleischhauer, Jan; Goerls, Helmar:

    A New Synthesis of Bis-Enaminones via Acylation of Ketones

    Image for article: A New Synthesis of Bis-Enaminones via Acylation of Ketones
  • 3081
    Sukemoto, Satoshi; Oshige, Miyo; Sato, Masahiro; Mimura, Ken-ichiro; Nishioka, Hiromi; Abe, Hitoshi; Harayama, Takashi; Takeuchi, Yasuo:

    Concise Asymmetric Synthesis of (+)-Febrifugine Utilizing trans-Selective Intramolecular Conjugate Addition

    Image for article: Concise Asymmetric Synthesis of (+)-Febrifugine Utilizing <EM EMTYPE="ITALIC">trans-</EM>Selective Intramolecular Conjugate Addition
  • 3088
    Stroganova, Tatyana A.; Vasilin, Vladimir K.; Zelenskaya, Elena A.; Red’kin, Viktor M.; Krapivin, Gennady D.:

    Some Transformations of Tertiary N-Furfurylamides of Aromatic and Heteroaromatic Carboxylic Acids under Acidic Conditions

    Image for article: Some Transformations of Tertiary <EM EMTYPE="ITALIC">N</EM>-Furfurylamides of Aromatic and Heteroaromatic Carboxylic Acids under Acidic Conditions
  • 3099
    Hämmerle, Johanna; Spina, Markus; Schnürch, Michael; Mihovilovic, Marko D.; Stanetty, Peter:

    A Comparative Study on Stille Cross-Coupling Reactions of 2-Phenylthiazoles and 2-Phenyloxazoles

    Image for article: A Comparative Study on Stille Cross-Coupling Reactions of 2-Phenylthiazoles and 2-Phenyloxazoles
  • 3108
    Tardy, Sébastien; Vicente, Joana Lobo; Tatibouët, Arnaud; Dujardin, Gilles; Rollin, Patrick:

    Carbohydrate-Based Spiro-1,3-oxazolidine-2-thiones: Stereoselective Approaches Using Aziridines and Epoxides

    Image for article: Carbohydrate-Based Spiro-1,3-oxazolidine-2-thiones: Stereoselective Approaches Using Aziridines and Epoxides
  • 3121
    Join, Benoit; Lohier, Jean-François; Delacroix, Olivier; Gaumont, Annie-Claude:

    Convenient Mild and Selective Hydrophosphination of Functionalized Alkenes: Access to P,O and P,S Derivatives

    Image for article: Convenient Mild and Selective Hydrophosphination of Functionalized Alkenes: Access to P,O and P,S Derivatives
  • 3126
    Heydari, Akbar; Khaksar, Samad; Tajbakhsh, Mahmood:

    1,1,1,3,3,3-Hexafluoroisopropanol: A Recyclable Organocatalyst for N-Boc Protection of Amines

    Image for article: 1,1,1,3,3,3-Hexafluoroisopropanol: A Recyclable Organocatalyst for <EM EMTYPE="ITALIC">N</EM>-Boc Protection of Amines
  • 3131
    Ghelfi, Franco; Pattarozzi, Mariella; Roncaglia, Fabrizio; Parsons, Andrew F.; Felluga, Fulvia; Pagnoni, Ugo M.; Valentin, Ennio; Mucci, Adele; Bellesia, Franco:

    Preparation of the Maleic Anhydride Nucleus from Dichloro γ-Lactams: Focus on the Role of the N-Substituent in the Functional Rearrangement and in the Hydrolytic Steps

    Image for article: Preparation of the Maleic Anhydride Nucleus from Dichloro γ-Lactams: Focus on the Role of the N-Substituent in the Functional Rearrangement and in the Hydrolytic Steps

    • special topic

  • 3142
    Luchetti, Giovanni; Ding, Kejia; d’Alarcao, Marc; Kornienko, Alexander:

    Enantio- and Diastereodivergent Synthetic Route to Multifarious Cyclitols from d-Xylose via Ring-Closing Metathesis

    Image for article: Enantio- and Diastereodivergent Synthetic Route to Multifarious Cyclitols from <EM EMTYPE="CAPS">d</EM>-Xylose via Ring-Closing Metathesis
  • 3148
    Luchetti, Giovanni; Ding, Kejia; Kornienko, Alexander; d’Alarcao, Marc:

    Synthesis of Differentially Protected myo- and chiro-Inositols from d-Xylose: Stereoselectivity in Intramolecular SmI2-Promoted Pinacol Reactions

    Image for article: Synthesis of Differentially Protected <EM EMTYPE="ITALIC">myo</EM>- and <EM EMTYPE="ITALIC">chiro</EM>-Inositols from <EM EMTYPE="CAPS">d</EM>-Xylose: Stereoselectivity in Intramolecular SmI<SUB>2</SUB>-Promoted Pinacol Reactions
  • 3155
    Prasad, Kavirayani R.; Pawar, Amit B.:

    Facile Enantiospecific Synthesis of Dihydroconduritols E and F

    Image for article: Facile Enantiospecific Synthesis of Dihydroconduritols E and F
  • 3160
    Chiara, Jose Luis; Bobo, Sofía; Sesmilo, Esther:

    Stereoselective Synthesis of Branched Cyclopentitols by Titanium(III)-Promoted Reductive Cyclization of 4-Oxiranylaldehydes and 4-Oxiranyl Ketones Derived from Hexoses

    Image for article: Stereoselective Synthesis of Branched Cyclopentitols by Titanium(III)-Promoted Reductive Cyclization of 4-Oxiranylaldehydes and 4-Oxiranyl Ketones Derived from Hexoses
  • 3167
    Sisa, Miroslav; Trapero, Ana; Llebaria, Amadeu; Delgado, Antonio:

    Small-Scale One-Pot Reductive Alkylation of Unprotected Aminocyclitols with Supported Reagents

    Image for article: Small-Scale One-Pot Reductive Alkylation of Unprotected Aminocyclitols with Supported Reagents
  • 3171
    Shan, Mingde; O’Doherty, George A.:

    Synthesis of Cyclitols via Cyclopropanation/Palladium-Catalyzed Ring Opening

    Image for article: Synthesis of Cyclitols via Cyclopropanation/Palladium-Catalyzed Ring Opening

    • practical synthetic procedures

  • 3180
    Ishikawa, Shunpei; Manabe, Kei:

    Synthesis of Substituted Monohalobenzenes via Ortho-Selective Cross-Coupling of Dihalobenzenes with Electron-Donating Ortho-Directing Groups

    Image for article: Synthesis of Substituted Monohalobenzenes via Ortho-Selective Cross-Coupling of Dihalobenzenes with Electron-Donating Ortho-Directing Groups