Novel Zirconium-Iron Multinuclear Complex Catalysts for Olefin Polymerizations
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概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 1996-10-15
著者
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Yamada T
Department Of Chemistry Faculty Of Science And Engineering Konan University
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Mukaiyama Teruaki
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Yamada Tohru
Basic Research Laboratories For Organic Synthesis Mitsui Petrochemical Industries Ltd.
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Yamada Tohru
Basic Research Laboratories For Polymer Chemistry Mitsui Petrochemical Industnes Ltd.
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Mitani M
Mitsui Chemicals Inc. Chiba Jpn
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Mitani Makoto
Basic Research Laboratories For Polymer Chemistry Mitsui Petrochemical Industnes Ltd.
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HAYAKAWA Michiya
Basic Research Laboratories for Polymer Chemistry, Mitsui Petrochemical Industnes, Ltd.
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Hayakawa Michiya
Basic Research Laboratories For Polymer Chemistry Mitsui Petrochemical Industnes Ltd.
関連論文
- Synthesis of Endomorphin-2Analogues Containing Piperidinecarboxylic Acid (Pip) and 2-Azetidinecarboxylic Acid (Aze)
- Peptide Synthesis Using Carbamoylmethyl Esters as Acyl Donors Mediated by Bacillus amyloliquefaciens Protease
- Synthesis and Conformational Study of Hexapeptides Containing α,α-Di(2-pyridyl)glycine
- Synthesis and Determination of Chirality of Optically Active α-Cyclopropylalanine
- Synthesis and Biological Activity of Endomorphin-2 Analogues Containing Pro Mimics
- Comparison of Conformations of Tetrapeptide Diastereomers Containing α-Phenyl-α-(2-pyridyl)glycine
- Utilization of Carica papaya Lipase for the Optical Resolution of Non-protein Amino Acids
- Synthesis and Conformational Study of Tripeptides Containing α,α-Disubstituted Glycine Having a Hetero-Aromatic Ring (2)
- Synthesis and Binding Activities of Endomorphin Analogs Containing 1-Aminocyclopropane-1-carboxylic Acid
- Synthesis and Conformational Study of Tripeptides Containing α, α-Disubstituted Glycine Having Hetro-Aromatic Ring
- Synthesis and Receptor-Binding Activity of Morphiceptin Analogs Containing α, α-Disubstituted Glycine in the Position 2
- Synthesis and Conformational Study of Tetrapeptide Diastereomers Containing α-Phenyl-α-(2-pyridyl)glycine
- Complexation Behavior of the Metal Ions with Peptides Containing α, α-Di(2-pyridyl)glycine (2Dpy)
- Solid-Phase Synthesis of Tripeptides Containing α, α-Disubstituted Glycine with Pyridine Rings (2)
- Synthesis and Separation of Diastereomers of Tripeptides Containing α, α-Di(2-pyridyl)glycine
- Chiral Recognition Ability of Quaternary Ammonium Salts by Tetrapeptides
- Synthesis and Conformational Study of Tripeptides Containing the Amino Acid with a Pyridine Ring
- Peptide Synthesis Using Carbamoylmethyl Esters as Acyl Donors Mediated by Microbial Proteases
- Study of the Enzymatic Degradation of Endomorphin Analogs Containing α, α-Disubstituted Glycine
- Fluorescence Behavior of Very Crowded Tripeptides Containing 9-Aminofluorene-9-carboxylic Acid
- Enantiomeric Separation of N-Protected Amino Acid Esters by Micellar Electrokinetic Chromatography Using t-Leucine Derivatives. II
- Conformations and Metal-Complex Formation of Tripeptides Containing, α, α-Disubstituted Glycine with Pyridine Rings
- Synthesis and Receptor-binding Activity of Endomorphin Analogs Containing α, α-Disubstituted Glycine
- Synthesis and Conformation of Tripeptides Containing α, α-Di(2-pyridyl)glycine
- Fluorescence Behavior of Peptides Containing 9-Aminofluorene-9-carboxylic Acid
- Facile Synthesis of Optically Active α-Methyl-α-amino Acids
- Synthesis of Oligopeptides Containing α, α-Diphenylglycine
- Peptide Synthesis Mediated by Bacillus subtilis Protease
- Superiority of the Carbamoylmethyl Ester as an Acyl Donor for the Protease-catalyzed Kinetically Controlled Peptide Synthesis in Organic Media: Application to Segment Condensations
- Enantiomeric Separation of N-Protected Amino Acid Esters by Micellar Electrokinetic Chromatography Using t-Leucine Derivatives
- Design of Peptides Containing an α,α-Disubstituted Glycine That Recognize Ammonium Salts
- Synthesis and Conformation of Peptides Containing 9-Aminofluorene-9-carboxylic Acid
- Synthesis and Conformational Analysis of Dnp-pNA Derivatives of Tetrapeptides Containing α, α-Dicyclopropylglycine
- α-Chymotrypsin-catalyzed Peptide Synthesis Using Esters of Aliphatic Amino Acids as Acyl Donors
- Side Reaction at the Hydrolysis of the Methyl Ester of Aib-Containing Peptide
- Optical Resolution of Amino Acids via Asymmetric Hydrolysis of Their Esters by Catalysis with Microbial Proteases
- Dramatic Differences in the Effectiveness among Various Coupling Methods in Synthesis of Peptides Containing α,α-Diphenylglycine
- A Catalytic Asymmetric Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Ketones Using a Chiral Titanium Oxide
- Stereoselective Synthesis of 1,2-cis-Arabinofuranosides Using a Titanium Catalyst
- Asymmetric Allylation of Carbonyl Compounds with Tartrate-Modified Chiral Allylic Tin Reagents
- Asymmetric Allylation of Aromatic Aldehydes Using Chiral Allylic Tin Reagents
- An Asymmetric Synthesis of the ABC Ring System of 8-Demethyltaxoids from Optically Active 8-Membered Ring Compound via Intramolecular Aldol and Pinacol Coupling Reactions
- An Asymmetric Synthesis of the BC Ring System of 8-Epitaxoids by Way of Intramolecular Aldol and Successive Stereoselective Methylation Reactions
- An Asymmetric Synthesis of the Fully Functionalized AB Ring System of 12-Demethyltaxol via Successive Stereoselective Allylation and Intramolecular Aldol Reactions
- New Synthesis of Pinacols By Oxidative Coupling Mediated by 1,2-Dusulfides as Dehydrogenating Reagents under Irradiation
- Magnesium Bromide Diethyl Etherate Mediated Highly Diastereoselective Aldol Reaction between an Aldehyde and a Silyl Enol Ether
- Aldol Reaction of Enol Esters Catalyzed by Cationic Species Paired with Tetrakis(pentafluorophenyl)borate
- A New and Efficient Method for Oxidation of Various Alcohols by Using N-tert-Butyl Phenylsulfinimidoyl Chloride
- A Novel Carbocationic Species Paired with Tetrakis(pentafluorophenyl)Borate Anion in Catalytic Aldol Reaction
- PREPARATION OF USEFUL SYNTHETIC INTERMEDIATES OF TAXOL ANALOGS, CYCLOOCTENONE DERIVATIVES
- Construction of AB-Ring System of Taxane Framework by A-Ring Annulation Strategy : Synthesis of 1-Hydroxy-8,11,11-trimethylbicyclo-[5.3.1]undec-7-en-9-one by Way of Intramolecular Aldol Cyclization to Form the C1-C10 Bond
- Synthesis and Determination of Chirality of Optically Active α-Cycloalkylalanines
- A New Method for the Synthesis of Unsymmetrical Bis-Aldols by the Samarium(II) Iodide-Mediated Aldol Reaction of Aldehydes with Aryl or Alkyl Oxiranyl Ketones
- Synthesis of 18-Demethyltaxoid via Stereoselective Allylation and Intramolecular Aldol Condensation Reactions
- Nitrous Oxide Oxdation of Scondary and Benzylic Alcohols Using Ruthenium Complex Catalyst
- A New and Convenient Method for the Preparation of Cyclooctanone Containing Bis-Aldol Skelton by Samarium(II) Iodide-mediated Intramolecular Aldol Cyclization of ω-Oxiranyl Keto Octanal
- A Synthesis of AB-Ring Model System of Taxane Framework by Way of Intramolecular Knoevenagel Cyclization
- A Novel Activating Agents of 'Disarmed' Thioglycosides, Combination of Trityl Tetrakis(pentafluorophenyl)borate, Iodine and 2,3-Dichloro-5,6-dicyano-p-benzoquinone (DDQ)
- Stereoselective Glycosylation of Thioglycosides Promoted by Respective Combinations of N-Iodo-or N-Bromosuccinimide and Trityl Tetrakis(pentafluorophenyl)borate.Application to One-Pot Sequential Synthesis of Trisaccharide
- The Trityl Tetrakis(pentafluorophenyl)borate Catalyzed Stereoselective Glycosylation Using New Glycosyldonor, 3, 4,, 6-Tri-O-benzyl-2-O-p-toluoyl-β-D-glucopyranosyl Phenylcarbonate
- Structural Studies of [2',6'-Dimethyl-L-tyrosine^1]Endomorphin-2 Analogues Containing Proline Mimics
- A Useful Method for the Preparation of Carboxylic Esters from Free Carboxylic Acids and Alcohols
- A Convenient Synthesis of Carboxanilides from Silyl Carboxylates and Weakly Nucleophilic Anilines Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Titanium (IV) Salt
- Facile Synthesis of Lactones from Silyl ω-Siloxycarboxylates Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Lewis Acid
- A New and Efficient Method for the Preparation of S-Phenyl Carbothioates via Mixed Anhydrides Using Active Titanium(IV) Salts
- An Efficient Method for the Preparation of Carboxylic Esters via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid
- The Catalytic Diels-Alder Reaction Using Combined Catalyst System of Diphenyltin Sulfide or Lawesson's Reagent and Silver Perchlorate
- An Asymmetric Synthesis of Fully Functionalized B Ring System of Taxol
- The Esterification Reaction between Silyl Derivatives of Carboxylic Acids and Alcohols by the Promotion of a Catalytic Amount of Lewis Acid
- Synthesis and Conformational Study of Tri- and Hexapeptides Containing α,α-Di(2-pyridyl)glycine
- Catalytic and Stereoselective Glycosylation with a Novel and Efficient Disarmed Glycosyl Donor : Glycosyl p-Trifluoromethylbenzylthio-p-trifluoromethylphenyl Formimidate
- Synthesis of Vicinal Bis(alkylthio) Derivatives by Reductive Coupling of Dithioacetals Derived from Aromatic Aldehydes with Low Valent Titanium Iodide Species
- Highly Enantioselective Cyclopropanation of Styrenes and Diazoacetates Catalyzed by 3-Oxobutylideneaminatocobalt(II) Complexes, Part 2. Semiempirical Analysis of Diastereo and Enantioselectivities
- Nitrous Oxide Oxidation of Olefins Catalyzed by Ruthenium Porphyrin Complexes
- A New Method for the Synthesis of Baccatin III
- Stereocontrolled Synthesis of the BC Ring System of Taxol
- Determination of Relative and Absolute Stereochemistry of Cephalosporolide D and Its Enantioselective Total Synthesis
- N_2O Oxidation of Phosphines Catalyzed by Low-Valent Nickel Complexes
- Enantioselective Borohydride Reduction of N-Diphenylphosphinyl Imines Using Optically Active Cobalt(II) Complex Catalysts
- Practical and Efficient Enantioselective Borohydride Reduction of Aromatic Ketones Catalyzed by Optically Active Cobalt(II)Complexes Using Pre-Modified Borohydride
- Enantioselective Borohydride Reduction of Ketones Catalyzed by Optically Active Cobalt(II)Complexes : Achievement of High Enantioselection by Modified Borohydrides with Furfuryl Alcohol Derivatives
- Convenient Method for One-pot Perparation of 1, 2-Diamines form Nitroolefins
- Stereoselective Synthesis of N-Acetyl-α-neuraminosyl-galactose Disaccharide
- A New Efficient Method for Catalytic Hydrolysis of Thioglycoside
- A Novel Catalyst System, Antimony(V) Chloride-Lithium Perchlorate(SbCl_5-LiClO_4), in the Friedel-Crafts Acylation Reaction
- Highly Stereoselective Synthesis of 1,2-trans-Glycosides Using p-Chlorobenzylated Glycosyl Carbonate as Glycosyl Donor
- Catalytic Stereoselective Synthesis of α-D-Galactopyranosides from 2, 3, 4, 6-Tetra-O-benzyl-D-galactopyranose and Several Alcoholic Nucleophiles
- Synthesis of Peptides Containing α, α-Dicyclopropylglycine
- Diastereoselective Aldol and Reformatsky Reactions of α-Halo Carbonyl Compounds and Aldehydes Mediated by Titanium(II) Chloride
- Efficient Diastereoselective Pinacol Reaction of Aliphatic and Aromatic Aldehydes by Combined Use of Newly Utilized Titanium (II) Bromide and Copper
- A Direct and Selective Syntheses of α, α-Dichloro-and α-Chloro-ethyl Ketones by the Reaction of Alkyl Carboxylates with 1, 1-Dichloroethyllithium
- Diastereoselective Aldol Reaction of α-Bromo Ketones with Aliphatic Aldehydes by Using Titanium(II) Chloride and Copper
- Efficient Method for Pinacol Coupling of Aromatic and Aliphatic Ketones by Using Titanium (II) Chloride and Zinc in the Presence of Pivalonitrile
- Efficient Method for the Preparation of Aromatic Bromides and Iodides by Ferrocenium Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate-Catalyzed Halogenation with Bromine and Iodine Monochloride
- Convenient and Selective Preparation of Mono-alkoxyphenylsilanes from Phenylsilane and Alcohols
- Novel Zirconium-Iron Multinuclear Complex Catalysts for Olefin Polymerizations
- Stereoselective Cyclopolymerization of 1,5-Hexadiene Using Novel Bis(ferrocenyl)zirconocene Catalyst
- Preparation of Narrow Polydispersity Polycaprolactone Catalyzed by Cationic Zirconocene Complexes
- A Novel Method for the Preparation of Optically Active Dipeptide. Chemo- and Stereoselective Reduction of 2-Hydroxyimino Amides with Samarium Diiodide
- Synthesis and Conformational Analysis of Homo-oligopeptides of α,α-Dicyclopropylglycine