DOI: 10.1055/s-00000083

Synlett

Issue 04 · Volume 2002 · March 2002 DOI: 10.1055/s-002-1582

account

  • 0533
    Yamamura, Shosuke; Nishiyama, Shigeru:

    Anodic Oxidation of Phenols Towards the Synthesis of Bioactive Natural Products

    Image for article: Anodic Oxidation of Phenols Towards the Synthesis of Bioactive Natural Products
  • 0544
    Nielsen, Mogens Brøndsted; Diederich, François:

    Modules for Acetylenic Scaffolding

    Image for article: Modules for Acetylenic Scaffolding

    • letter

  • 0553
    Marié, Jean-Charles; Courillon, Christine; Malacria, Max:

    Compared Behaviors of trans- and cis-α,β-Epoxy-γ,δ-vinyl-silanes Towards Nucleophiles and Bases: High Regioselective Ring Opening and Deprotonation

    Image for article: Compared Behaviors of <EM EMTYPE="ITALIC">trans</EM>- and <EM EMTYPE="ITALIC">cis</EM>-α,β-Epoxy-γ,δ-vinyl-silanes Towards Nucleophiles and Bases: High Regioselective Ring Opening and Deprotonation
  • 0557
    Zerkowski, Jonathan A.; Hensley, Laura M.; Abramowitz, David:

    Triazinyl-Amino Acids, New Building Blocks for Pseudopeptides

    Image for article: Triazinyl-Amino Acids, New Building Blocks for Pseudopeptides
  • 0561
    Yamamoto, Yuhei; Maeda, Kenji; Tomimoto, Koji; Mase, Toshiaki:

    Lithiation of Aryl Bromides Possessing α-Proton of Carbonyl Groups

    Image for article: Lithiation of Aryl Bromides Possessing α-Proton of Carbonyl Groups
  • 0565
    Chittimalla, Santhosh Kumar; Liao, Chun-Chen:

    The Diels-Alder Reactions of 6,6-Dimethoxycyclohexa-2,4-dienone Generated by Pyrolysis of its Dimer

    Image for article: The Diels-Alder Reactions of 6,6-Dimethoxycyclohexa-2,4-dienone Generated by Pyrolysis of its Dimer
  • 0569
    Tanaka, Shinobu; Nakamura, Tomoaki; Yorimitsu, Hideki; Oshima, Koichiro:

    Radical Addition to (2,3-Epoxy-4-pentenyloxy)trialkylsilanes Yielding α,β-Unsaturated Aldehydes via Carbon-carbon Bond Cleavage

    Image for article: Radical Addition to (2,3-Epoxy-4-pentenyloxy)trialkylsilanes Yielding α,β-Unsaturated Aldehydes via Carbon-carbon Bond Cleavage
  • 0573
    Kumar, Subodh; Kaur, Pervinder; Chimni, Swapandeep Singh:

    The Efficient Allylations of 2-Oxocarboxylic Acids. Synthesis of 2-Allyl Derivatives of 2-Hydroxycarboxylic Acids

    Image for article: The Efficient Allylations of 2-Oxocarboxylic Acids. Synthesis of 2-Allyl Derivatives of 2-Hydroxycarboxylic Acids
  • 0575
    Sasaki, Kouji; Komatsu, Naoki; Shirakawa, Seiji; Maruoka, Keiji:

    Chemoselective Reduction of Saturated Aldehydes and Ketones over Unsaturated Carbonyls with Bowl-shaped Tris(2,6-diphenylbenzyl)tin Hydride

    Image for article: Chemoselective Reduction of Saturated Aldehydes and Ketones over Unsaturated Carbonyls with Bowl-shaped Tris(2,6-diphenylbenzyl)tin Hydride
  • 0577
    Shirakawa, Seiji; Komatsu, Naoki; Iwasaki, Atsuko; Maruoka, Keiji:

    Unusually Stable Silyl Ketones with Bowl-shaped Tris(2,6-diphenylbenzyl)-silyl Group for Various Nucleophilic Attacks and α-Deprotonation

    Image for article: Unusually Stable Silyl Ketones with Bowl-shaped Tris(2,6-diphenylbenzyl)-silyl Group for Various Nucleophilic Attacks and α-Deprotonation
  • 0580
    Page, Philip C. Bulman; Rassias, Gerasimos A.; Barros, David; Ardakani, Adel; Bethell, Donald; Merifield, Eric:

    New Organocatalysts for the Asymmetric Catalytic Epoxidation of Alkenes Mediated by Chiral Iminium Salts

    Image for article: New Organocatalysts for the Asymmetric Catalytic Epoxidation of Alkenes Mediated by Chiral Iminium Salts
  • 0583
    Page, Philip C. Bulman; Hayman, Colin M.; McFarland, Heather L.; Willock, David J.; Galea, Natasha M.:

    An IMDA Approach to Tigliane and Daphnane Diterpenoids: Generation of Rings A, B and C Incorporating C-18

    Image for article: An IMDA Approach to Tigliane and Daphnane Diterpenoids: Generation of Rings A, B and C Incorporating C-18
  • 0588
    Takai, Shigeyuki; Ploypradith, Poonsakdi; Hamajima, Akinari; Kira, Kazunobu; Isobe, Minoru:

    Sodium Hypophosphite Decomplexation of Acetylenebiscobalthexacarbonyls to cis-Olefins

    Image for article: Sodium Hypophosphite Decomplexation of Acetylenebiscobalthexacarbonyls to <EM EMTYPE="ITALIC">cis</EM>-Olefins
  • 0593
    González-Temprano, Inés; Sotomayor, Nuria; Lete, Esther:

    Highly Diastereoselective Intramolecular α-Amidoalkylation Reactions of Hydroxylactams Derived from N-Phenethylimides. Enantioselective Synthesis of Dihydropyrrolo[2,1-a] isoquinolones

    Image for article: Highly Diastereoselective Intramolecular α-Amidoalkylation Reactions of Hydroxylactams Derived from <EM EMTYPE="ITALIC">N</EM>-Phenethylimides. Enantioselective Synthesis of Dihydropyrrolo[2,1-<EM EMTYPE="ITALIC">a</EM>] isoquinolones
  • 0598
    Stavber, Stojan; Kralj, Petra; Zupan, Marko:

    Selective and Effective Iodination of Alkyl-substituted Benzenes with Elemental Iodine Activated by SelectfluorΤΜ F-TEDA-BF4

    Image for article: Selective and Effective Iodination of Alkyl-substituted Benzenes with Elemental Iodine Activated by Selectfluor<SUP>Τ</SUP><SUP>Μ</SUP> F-TEDA-BF<SUB>4</SUB>
  • 0601
    Mori, Yuichiro; Nakamura, Masayuki; Wakabayashi, Takeshi; Mori, Kouhei; Kobayashi, Shū:

    Efficient Total Synthesis of Khafrefungin: Convergent Approach Using Suzuki Coupling under Thallium-free Conditions Toward Multigram-scale Synthesis

    Image for article: Efficient Total Synthesis of Khafrefungin: Convergent Approach Using Suzuki Coupling under Thallium-free Conditions Toward Multigram-scale Synthesis
  • 0604
    Yadav, Jhillu S.; Reddy, Basi V. S.; Venugopal, Chenna; Ramalingam, T.:

    LiBF4-Mediated Conversion of Aldehydes to gem-Diacetates

    Image for article: LiBF<SUB>4</SUB>-Mediated Conversion of Aldehydes to <EM EMTYPE="ITALIC">gem</EM>-Diacetates
  • 0607
    Milne, Jacqueline E.; Jarowicki, Krzysztof; Kocienski, Philip J.:

    The Preparation of 6-Bromo-3,4-dihydro-2H-pyrans from Tetrahydropyran-2-ones via a Ni(0)-catalysed Coupling Reaction and their Halogen-metal Exchange to 6-Lithio-3,4-dihydro-2H-pyrans.

    Image for article: The Preparation of 6-Bromo-3,4-dihydro-2<EM EMTYPE="ITALIC">H</EM>-pyrans from Tetrahydropyran-2-ones via a Ni(0)-catalysed Coupling Reaction and their Halogen-metal Exchange to 6-Lithio-3,4-dihydro-2<EM EMTYPE="ITALIC">H</EM>-pyrans.
  • 0610
    Minisci, Francesco; Recupero, Francesco; Fontana, Francesca; Bjørsvik, Hans-René; Liguori, Lucia:

    Highly Selective and Efficient Conversion of Alkyl Aryl and Alkyl Cyclopropyl Ketones to Aromatic and Cyclopropane Carboxylic Acids by Aerobic Catalytic Oxidation: A Free-radical Redox Chain Mechanism.

    Image for article: Highly Selective and Efficient Conversion of Alkyl Aryl and Alkyl Cyclopropyl Ketones to Aromatic and Cyclopropane Carboxylic Acids by Aerobic Catalytic Oxidation: A Free-radical Redox Chain Mechanism.
  • 0613
    Makino, Kazuishi; Henmi, Yoshiaki; Hamada, Yasumasa:

    Synthetic Studies on a Cyclic Hexadepsipeptide GE3: Stereoselective Construction of the Acyl Side Chain Segment

    Image for article: Synthetic Studies on a Cyclic Hexadepsipeptide GE3: Stereoselective Construction of the Acyl Side Chain Segment
  • 0616
    Kim, Sung Soo; Nehru, Kasi:

    A Mild and Efficient Oxidation of Alcohols to Carbonyl Compounds by Periodic Acid Catalyzed by 2,2,6,6-Tetramethylpiperidinyl-1-oxyl

    Image for article: A Mild and Efficient Oxidation of Alcohols to Carbonyl Compounds by Periodic Acid Catalyzed by 2,2,6,6-Tetramethylpiperidinyl-1-oxyl
  • 0619
    Friedrich, Marko; Wächtler, Andreas; de Meijere, Armin:

    Extending the Scope of a Known Furan Synthesis - A Novel Route to 1,2,4-Trisubstituted Pyrroles

    Image for article: Extending the Scope of a Known Furan Synthesis - A Novel Route to 1,2,4-Trisubstituted Pyrroles
  • 0622
    Waldvogel, Siegfried R.:

    The Reaction Pattern of the MoCl5-Mediated Oxidative Aryl-aryl Coupling

    Image for article: The Reaction Pattern of the MoCl<SUB>5</SUB>-Mediated Oxidative Aryl-aryl Coupling
  • 0625
    Srinivas, K. V. N. S.; Reddy, E. Bolla; Das, Biswanath:

    Highly Convenient and Efficient One-pot Conversions of Aldehydes into Nitriles and Ketones into Amides Using HY-Zeolite

    Image for article: Highly Convenient and Efficient One-pot Conversions of Aldehydes into Nitriles and Ketones into Amides Using HY-Zeolite
  • 0628
    Gros, Philippe; Viney, Cédric; Fort, Yves:

    Ring Selective Lithiation of 3,5-Lutidine. A New Route to Heterocyclic Building Blocks.

    Image for article: Ring Selective Lithiation of 3,5-Lutidine. A New Route to Heterocyclic Building Blocks.
  • 0631
    Jang, Doo Ok; Cho, Dae Hyan:

    A Radical Carbon-carbon Bond Forming Reaction: Indium Mediated Radical Addition to β-Substituted Conjugated Alkenes in Aqueous Media

    Image for article: A Radical Carbon-carbon Bond Forming Reaction: Indium Mediated Radical Addition to β-Substituted Conjugated Alkenes in Aqueous Media
  • 0634
    Ishiwata, Akihiro; Takatani, Maki; Nakahara, Yoshiaki; Ito, Yukishige:

    Synthesis of N-Linked Glycosyl Asparagine Derivatives with Unprotected Sugar Components

    Image for article: Synthesis of <EM EMTYPE="ITALIC">N</EM>-Linked Glycosyl Asparagine Derivatives with Unprotected Sugar Components
  • 0637
    Kuroboshi, Manabu; Waki, Yoko; Tanaka, Hideo:

    Tetrakis(dimethylamino)ethylene (TDAE)-Pd Promoted Reductive Homo-coupling of Aryl Halides

    Image for article: Tetrakis(dimethylamino)ethylene (TDAE)-Pd Promoted Reductive Homo-coupling of Aryl Halides
  • 0640
    Hussain, Iqbal; Komasaka, Tatsuhiko; Ohga, Masanori; Nokami, Junzo:

    Racemization of Homoallyl Alcohols via an Allyl-transfer Reaction

    Image for article: Racemization of Homoallyl Alcohols via an Allyl-transfer Reaction
  • 0643
    Lakner, Frederick J.; Negrete, George R.:

    A New and Convenient Chiral Auxiliary for Asymmetric Diels-Alder Cycloadditions in Environmentally Benign Solvents

    Image for article: A New and Convenient Chiral Auxiliary for Asymmetric Diels-Alder Cycloadditions in Environmentally Benign Solvents
  • 0646
    Motherwell, William B.; Storey, Lynda J.:

    The Trifluoromethylacetophenone-N,N-dimethyltrimethylsilylamine Adduct - A New Shelf Stable Reagent for Nucleophilic Trifluoromethylation.

    Image for article: The Trifluoromethylacetophenone-<EM EMTYPE="ITALIC">N,N</EM>-dimethyltrimethylsilylamine Adduct - A New Shelf Stable Reagent for Nucleophilic Trifluoromethylation.

    • spotlight

  • 0649
    Gunanathan, Chidambaram:

    Lithium Perchlorate/Diethyl Ether (LPDE)