DOI: 10.1055/s-00000083

Synlett

Issue 11 · Volume 1998 · November 1998 DOI: 10.1055/s-002-275

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  • 1167
    Ohno, M.:

    Highly Selective Synthesis of Polyfunctionalized Carbo- and Heterocycles Based on Ring Expansion of Squaric Acid Derivatives

  • 1175
    Grimme, Wolfram; Bertsch, Achim; Flock, Holger; Noack, Thorsten; Krauthäuser, Susanne:

    Bridged Medium Rings with Hyperstable Double Bonds - Syntheses and Reactions

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  • 1182
    Enders, Dieter; Lochtman, René; Meiers, Michaela; Müller, Stephan; Lazny, Ryszard:

    Efficient N-N Bond Cleavage of Chiral Trisubstituted Hydrazines with BH3 ⋅ THF

  • 1185
    Bach, T.; Krüger, L.:

    Regioselective Pd(0)-Catalyzed Coupling Reactions on Methyl 2,3-Dibromofuran-5-carboxylate as a Facile Entry into 2,3,5-Tri- and 2,3-Disubstituted Furans

  • 1187
    Nayak, Sandip K.; Thijs, Lambertus; Zwanenburg, Binne:

    Diastereoselective Carbonyl-Ene Reactions of N-Trityl Aziridine-2-(S)-Carboxaldehyde

  • 1189
    Jin, Yonghao; Kim, Dong H.:

    A Practical Method for the Conversion of β-Hydroxy Carboxylic Acids into the Corresponding β-Amino Acids

  • 1191
    Huang, Xian; Duan, De-Hui:

    A Novel Synthetic Approach to β-Arylselenenyl Tertiary Alcohols by the One-Pot Reaction of Chloromethyl Selenides and Ketones Promoted by Samarium Diiodide

  • 1193
    Wamhoff, Heinrich; Warnecke, Heiko; Sohár, Pál; Csámpai, Antal:

    New Access to 7-Membered Heterocyclic C-Glycosides by the Cyclo-Addition-Ring-Expansion (CARE)-Reaction

  • 1195
    Polat, Tülay; Du, Yuguo; Linhardt, Robert J.:

    A General Method for the Stereospecific Synthesis of C-Glycosides of Ulosonic acids by Samarium-Mediated Reductive Dechlorination

  • 1197
    Cerè, Vanda; Peri, Francesca; Pollicino, Salvatore; Ricci, Alfredo:

    First Example of a New Class of Conduritols: the 2,3-Diamino Derivatives. Simple and Efficient Synthesis of the (1R,2R,3R,4R)-(-)-2,3-Diamino-1,4-dimethoxycyclohex-5-ene 2

  • 1199
    Zumpe, Franz L.; Kazmaier, Uli:

    A Mild Palladium Catalyzed N-Allylation of Amino Acids and Peptides

  • 1201
    Arai, Shigeru; Oku, Makoto; Miura, Motoko; Shioiri, Takayuki:

    Catalytic Asymmetric Epoxidation of Naphthoquinone Derivatives Under Phase-Transfer Catalyzed Conditions

  • 1203
    Choudary, B. M.; Lakshmi Kantam, M.; Bharathi, B.; Venkat Reddy, Ch.:

    Superactive Mg-Al-O-t-Bu Hydrotalcite for Epoxidation of Olefins

  • 1205
    Wölfling, János; Frank, Éva; Schneider, Gyula; Bes, Maria Teresa; Tietze, Lutz F.:

    Synthesis of Azasteroids and d-Homosteroids by Intramolecular Cyclization Reactions of Steroid Arylimines

  • 1207
    Drechsler, Ulf; Hanack, Michael:

    An Easy Route from Catechols to Phthalonitriles

  • 1209
    Shimizu, Atsushi; Nishiyama, Shigeru:

    Synthetic Approaches towards Laulimalide: Synthesis of the C12-C29 Fragment

  • 1211
    Heumann, Andreas; Moukhliss, Maati:

    Cycloisomerisation of 1,6-Dienes in the Presence of Cationic Palladium Catalysts

  • 1213
    Hu, Yulai; Yu, Jianhua; Yang, Shiyan; Wang, Jin-Xian; Yin, Yuanqi:

    Nickel(II) Catalyzed Substitution Reactions of Nitro Group on 1-aryl-2-nitroethenes by Organozinc Halides

  • 1215
    Demircan, Aydin; Parsons, Philip J.:

    Radical Addition to Substituted Furans: Diels-Alder Like Products Versus Fragmentation Reactions

  • 1217
    Zong, Kyukwan; Shin, Seung Il; Kim, Hyoung Rae; Ryu, Eung K.:

    A Facile Synthesis of 1,2,4-Oxadiazolidin-3-ones via Tandem O,N-Addition of Hydroxyureas to Methyl Propiolate

  • 1219
    Krief, Alain; Dumont, Willy; Markó, István E.; Murphy, Fiona; Vanherck, Jean-Christophe; Duval, Romain; Ollevier, Thierry; Abel, Ulrich:

    Preparation and Synthetic Utility of 2-Methylselenomethyl Allyl Methyl Selenide. A Valuable Precursor to 2-Silylmethylallyllithiums

  • 1223
    Demont, Emmanuel; Lopez, Roman; Férézou, Jean-Pierre:

    Stereoselective Synthesis of the C1-C5 Dienoic Sub-unit of Bafilomycins via a γ-Sulfonyl-δ-Lactone Intermediate

  • 1227
    Berteina, Sabine; De Mesmaeker, Alain:

    Radical and Palladium-Mediated Cyclizations of Ortho-Iodo Benzyl Enamines: A Scope and Limitation Study

  • 1231
    Berteina, Sabine; Wendeborn, Sebastian; De Mesmaeker, Alain:

    Radical and Palladium-Mediated Cyclization of Ortho-Iodo Benzyl Enamines: Application to Solid Phase Synthesis

  • 1234
    Almirante, Nicoletta; Cerri, Alberto; De Munari, Sergio:

    Stereoselective Synthesis of New Digitalis-like Perhydroindene Derivatives from the Hajos-Parrish Ketone

  • 1237
    Jotterand, Nathalie; Vogel, Pierre:

    Stereoselective Synthesis of New Conduramines and Aminocyclitol Derivatives

  • 1240
    Schmidt, Boris; Kühn, Christian:

    Racemic, Yet Diastereomerically Pure Azido Acids as Both γ-Turn and Inverse γ-Turn Mimetics for Solid-Phase Peptide Synthesis

  • 1243
    Kiss, LászlóE.; Rábai, József; Varga, László; Kövesdi, István:

    Methyl Perfluorooctanethionate as a Tool for Indirect Perfluoroalkylmethylation and Perfluoroalkylation of Amines

  • 1246
    Ikeda, Masazumi; Hamada, Masahiro; Yamashita, Takashi; Ikegami, Fumi; Sato, Tatsunori; Ishibashi, Hiroyuki:

    Formal Synthesis of (±)-Pancracine Using Stereoselective Radical Cyclization of N-(2-Cyclohexenyl)-α-aryl-α-(phenylthio)acetamide

  • 1249
    Le Roux, C.; Ciliberti, L.; Laurent-Robert, H.; Laporterie, A.; Dubac, J.:

    Bismuth(III) Triflate: A Water-Stable Equivalent of Trimethylsilyl Triflate for the Catalysis of Mukaiyama Aldol Reactions

  • 1252
    Fuganti, Claudio; Serra, Stefano:

    A New Enantioselective Route to Bisabolane Sesquiterpenes Phenols: Synthesis of (S)-(+)-Curcuphenol and (S)-(+)-Curcumene

  • 1255
    Humilière, Delphine; Thorimbert, Serge; Malacria, Max:

    A New Enantioselective Synthesis of Highly Functionalized Cyclopentanols

  • 1258
    Forsee, Jennifer E.; Smith, Brent T.; Frank, Kristine E.; Aubé, Jeffrey:

    Reactions of Oxazolinium and Dihydrooxazinium Salts Prepared by an Azide Insertion Sequence: pH Control of Product Distribution

  • 1261
    Takahashi, Takashi; Tomida, Satoshi; Inoue, Hitoshi; Doi, Takayuki:

    Nucleophilic Substitutions on MultipinTM Systems Linked with a Traceless Linker

  • 1264
    Craig, Donald; Payne, Andrew H.; Warner, Peter:

    Template-Directed Intramolecular C-Glycosidation. Synthesis of the Central Tetrahydrofuran Fragment of the Elfamycin Antibiotic Aurodox

  • 1267
    Shimizu, Masaki; Sasaki, Tomoya; Hiyama, Tamejiro:

    Facile Synthesis of 1-Sila-4-stannacyclohexanes from 1,5-Distannyl-3-silapentanes

  • 1270
    Sugamoto, Kazuhiro; Hamasuna, Yutaka; Matsushita, Yoh-ichi; Matsui, Takanao:

    A Synthesis of Oximes from Olefins by Cobalt(II) Porphyrin-Catalyzed Reduction-Nitrosation

  • 1273
    Chaudhuri, Gopeswar; Chowdhury, Chinmay; Kundu, Nitya G.:

    A Highly Stereoselective Synthesis of (Z)-N-Aryl(alkyl)-2-arylidine-2,3-dihydro-1,4-benzoxazines through Palladium Catalyzed Reactions

  • 1276
    Thoresen, Lars H.; Kim, Heejin; Welch, Mike B.; Burghart, Armin; Burgess, Kevin:

    Synthesis of 3,5-Diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY®) Dyes

  • 1279
    Poupardin, Olivia; Greck, Christine; Genêt, Jean-Pierre:

    Rapid Asymmetric Synthesis of Highly Functionalized C5 Chiral Synthons. Practical Preparation of trans-3-Hydroxy-D-Proline

  • 1282
    Rodríguez, G.; Rodríguez, D.; López, M.; Castedo, L.; Domínguez, D.; Saá, C.:

    Synthesis of Dibenzodiynes: Exceptionally Easy Formation of a Chrysene Biradical

  • 1285
    Burks, Eric; Koshti, Nirmal; Jacobs, Hollie; Gopalan, Aravamudan:

    Selective Monohydrolysis of Esters of Polyaminocarboxylic acids using Pig Liver Esterase

  • 1288
    Alajarín, Mateo; Molina, Pedro; Vidal, Ángel; Tovar, Fulgencio:

    The First Aza-Wittig Reaction of the β-Lactam Carbonyl Group

  • 1291
    Ishikawa, Teruhiko; Nagai, Keita; Kudoh, Takayuki; Saito, Seiki:

    Chiral Lewis Acid-Hydroxylamine Hybrid Reagent for Enantioselective Michael Addition Reaction Directed Towards β-Amino Acids Synthesis

  • 1294
    Ochse, Michael:

    The Atropo-Divergent Preparation of Axially Chiral Biaryls Through the `Lactone Methodology': Total Synthesis of Korupensamine B