Total Syntheses of Bistratamides J, E, and H from Two Types of ΔAla-Containing Oligopeptides

スポンサーリンク

概要

• 論文の詳細を見る
• 2008-04-15

著者

• SATO Ken-ichi

  Laboratory of Molecular Biology, Biosignal Research Center, Kobe University

• SUZUKI Hiroyuki

  Laboratory of Biomedical Research, Institute of Molecular and Cellular Biosciences, University of To

• Shin Chung-gi

  Laboratory Of Organic Chemistry Faculty Of Engineering Kanagawa University

• Shin Chung-gi

  Laboratory Of Oraganic Chemistry Faculty Of Engineering Kanagawa University

• AKAI Shoji

  Laboratory of Organic Chemistry, Faculty of Engineering, Kanagawa University

• Yonezawa Yasuchika

  Laboratory Of Oraganic Chemistry Faculty Of Engineering Kanagawa University

• Akai Shoji

  Laboratory Of Organic Chemistry Faculty Of Engineering Kanagawa University

• ANDOH Masanori

  Laboratory of Organic Chemistry, Faculty of Engineering, Kanagawa University

• Andoh Masanori

  Laboratory Of Organic Chemistry Faculty Of Engineering Kanagawa University

• Sato Ken-ichi

  Laboratory of Chemistry for Natural Products, Faculty of Science, Tokyo Institute of Technology

関連論文

• Hydrogen peroxide induces Src family tyrosine kinase-dependent activation of Xenopus eggs
• A Novel Mutant from Apoptosis-resistant Colon Cancer HT-29 Cells Showing Hyper-apoptotic Response to Hypoxia, Low Glucose and Cisplatin
• Total Synthesis of a Macrocyclic Antibiotic, Micrococcin P_1
• Total Synthesis of a Macrocyclic Antibiotic, Micrococcin P
• Convenient Synthesis of the Central 3,6-Di(2-thiazolyl)-2-(4-thiazolyl)-pyridine Skeleton of a Macrocyclic Antibiotic, GE 2270 A
• Synthesis of a Fragment A Derivative of an Antibiotic, Nosiheptide
• Total Synthesis of Antibiotic, Micrococcin P, from 2, 3, 6-Polythiazolesubstituted Pyridine Skeleton[Fragment A-C]
• Synthesis of the Central Heterocyclic Skeleton of an Antibiotic, A10255
• Useful Synthesis of 2, 3, 6-Polythiazolesubstituted Pyridine Skeleton [Fragment A-C]of Peptide Antibiotic, Micrococcin P
• Dehydrooligopeptides. XIV. Syntheses of 2-[(Z)-1-Amino-1-alken-1-yl]oxazole-4-carboxylic Acid and the Main Common Skeleton of Thiostrepton Peptide Antibiotics, A10255G and J^
• Syntheses of 2-[(1S,3S)-1-Amino-3-carboxy-3-hydroxypropyl]-thiazole-4-carboxylic Acid and the Tripeptide Skeleton of Nosiheptide Containing the Acid
• Dehydrooligopeptides. XVII. Practical Syntheses of All of the Diastereomers of N,N-Protected 2,3-Diaminobutanoic Acids from L-and D-Threonine Derivatives
• A Convenient Synthesis of Methyl 2-[2-(Amino)ethenyl-bithiazolyl] thiazoline-4-carboxylate, an Important Skeleton of Cyclothiazomycin
• Synthesis of a Common Main Skeleton of Thiostrepton Peptide Antibiotics, A 10255G and J
• Practical Synthesis of Oligodehydroalanine Derivatives by Repetition of Stepwise Elongation of Serine Derivative and β-Elimination
• Practical Synthesis of Oxazoles Incorporated in α-Dehydroamino Acid and Dehydropeptide Structures
• Convenient Syntheses of Thiazoles Incorporated with α-Dehydroamino Acid and Dehydropeptide Structures
• Crystal Structure of(1R, 2R, 3S, 4S, 5S, 6S, 7R, 9S)-6-Azido-7-cyano-3-C-hydroxy-methyl-3, 3'-di-O-isopropylidene-9-methoxy-2, 4, 5-tris(O-methoxymethyl)-2, 3, 4, 5-tetrahydroxy-8-oxabicyclo[4. 3. 0]nonane, toward Tetrodotoxin
• Total Synthesis of Bistratamides G and H from Various Kinds of ΔAla and ΔAbu-Containing Oligopeptides
• Convenient Syntheses of 3-Deoxy-D-manno-2-octulosonic Acid (KDO) and 3-Deoxy-D-glycero-D-galacto-2-nonulosonic Acid (KDN) Derivatives from D-Mannose
• Convenient Synthesis of the Main Dehydrohexapeptide Skeleton Constituting a Macrocyclic Antibiotic, Berninamycin A
• Useful Synthesis of the Main Dehydrohexapeptide Segment of a Macrocyclic Antibiotic, Berninamycin B
• Total Syntheses of Bistratamides J, E, and H from Two Types of ΔAla-Containing Oligopeptides
• Useful Intermediates, 3-C-Dichloromethyl Furanose Derivatives, for the Synthesis of Branched-Chain Functionalized Sugars
• Novel Synthesis of the Main Central 2,3,6-Trisubstituted Pyridine Skeleton [Fragment A-B-C] of a Macrobicyclic Antibiotic, Cyclothiazomycin
• Convenient Synthesis of a Central 2,3,6-Trisubstituted Pyridine Skeleton of a Macrobicyclic Antibiotic, Cyclothiazomycin
• Useful Synthesis of Fragment A-C-D of a Thiostrepton-type Macrocyclic Antibiotic, Thiocilline I
• Total Synthesis of Bistratamide G, a Metabolite of the Philippines Ascidian Lissoclinum bistratum, from Dehydrotripeptides
• Convenient Synthesis of the Main Tridehydropentapeptide Skeleton for a Macrocyclic Antibiotic, Sulfomycin I
• Asymmetric Synthesis of the Main Pyridine Skeleton for a Macrobicyclic Antibiotic, Cyclothiazomycin
• Convenient Synthesis of (3S, 5S)-5-Hydroxy- and (3R, 5S)-5-Chloropiperazic Acids of a Peptide Antibiotic, Monamycin G^3
• Dehydrooligopeptides. XX. Unusual Peptide Bond Cleavage of Dehydrotripeptide Esters Containing α-Dehydroamino Acid Residue at P_2 by Using Papain
• Dehydrooligopeptides. XVIII. Enzymatic Hydrolysis and Coupling of Dehydrodipeptide Esters Containing α-Dehydroamino Acid Residue by Using Papain
• Convenient Synthesis of Dehydrooligopeptides Containing α-Dehydroamino Acid Residue Alone
• Crystal Structure of Potential Key Compounds, DL-(1, 2, 3', 4, 5, 6'/3, 6)-6-Azido-5'-O-t-butyldiphenylsilyl-6-(cyano)hydroxymethyl-3, 5-di-C-hydroxymethyl-1, 2 : 3, 3'-di-O-isopropylidene-4-O-methoxymethyl-1, 2, 3, 4-cyclohexanetetrol, toward(±)-Tetrodot
• An Efficient Deoxysugar Synthesis using Bu4NBH4 via an SN2 Reduction
• Total Synthesis of a Novel β-Glucosidase Inhibitor, Cyclophellitol Starting from D-Glucose
• Reaction of α-Hydroxydichloromethyl Derivatives with Cesium Acetate
• A Novel Method for Constructions of β-D-Mannosidic, 2-Acetamido-2-deoxy-β-D-mannosidic, and 2-Deoxy-β-D-arabino-hexopyranosidic Units from the Bis(triflate) Derivative of β-D-Galactoside
• A Novel Method for Constructing β-D-Mannosidic, 2-Acetamido-2-deoxy-β-D-mannosidic, and 2-Deoxy-D-arabino-hexopyranosidic Units from the Bis(triflate) Derivative of β-D-Galactoside
• Facile Syntheses of (s, s)-2, 3-Diaminobutyric Acid and the Acid Containing N-Terminal Tripeptide of Antrimycins
• Branched-chain Sugars. XXIX. Synthesis of Moenuronic Acid (4-C-Methyl-D-glucuronic Acid)
• Branched-chain Sugars. IX. Reaction of 3,6-Anhydro-1,2-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose with Nitromethane or Hydrogen Cyanide
• Branched-chain Sugars. VIII. On the Configuration of Branched-chain Sugars from Methyl 3-O-Benzoyl-4,6-O-benzylidene-α-D-arabino-hexopyranosid-2-ulose
• Branched-chain Sugars. XXIII. Stereoselectivities in the Addition of Nucleophiles to Several 4-Uloses
• Branched-chain Sugars. VI. Reaction of Methylene Dimagnesium Bromide with Uloses
• Branched-chain Sugars. XXIV. Synthesis of Methyl 6-Deoxy-3-C-methyl-β-D-gulopyranoside (Methyl β-Virenoside)
• Branched-chain Sugars. XX. Kinetic Studies on the Epimerization of 1,2 : 5,6-Di-O-isopropylidene-3-C-nitromethyl-α-D-allofuranose
• α,β-Unsaturated Carboxylic Acid Derivatives. IV. General Synthesis of Unsaturated Unsymmetric 3,6-Disubstituted-2,5-piperazinediones
• Aminosugars. XXVIII. A Facile Synthesis of Benzyl α- and β-Kasugaminides via the Corresponding Abequosides
• Branched-chain Sugars. XII. The Stereoselectivities in the Reaction of Methyl 4,6-O-Benzylidene-α- and -β-D-hexopyranosid-3-uloses with Diazomethane
• Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses
• Branched-chain Sugars. XIX. On the Application of 13C NMR Spectroscopy to the Configurational Assignment of 3-C-Substituents of Aldohexopyranose Derivatives
• Dehydrooligopeptides. XIII. Selective Enzymatic Hydrolysis of N-Protected .ALPHA.-Dehydroglutamic Acid Diesters and Their Analogs Using Papain as Catalyst.
• Dehydrooligopeptides. X. Useful synthetic method for (E)- and (Z)-isomers of dehydroaspartic acids, and their .DELTA.1,2-dehydrodipeptides by the base-catalyzed .BETA.-elimination.
• The synthesis and reaction of spiro(oxolane-2,2'-piperazine)-3',6'-diones with N-bromosuccinimide in the presence or absence of water.
• Synthesis of (3Z, 6E)-1-N-Methylalbonoursin, a New Metabolite from Streptomyces albus
• Dehydrooligopeptides. VIII. Convenient syntheses of various dehydrotyrosine derivatives protected with useful N,O-protecting groups via N-carboxy dehydrotyrosine anhydrides.
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XIII. The synthesis and configuration of alkyl 2-acylamino-2-alkenoates and their cyclized 2,5-piperazinedione derivatives.
• Dehydrooligopeptides. XI. Facile syntheses of various kinds of dehydrodi- and tripeptides, and dehydroenkephalins containing .DELTA.Tyr residue by using N-carboxydehydrotyrosine anhydride.
• Dehydrooligopeptides. IX. Syntheses and conversions of .ALPHA.-dehydroglutamine derivatives to N-carboxy-.ALPHA.-dehydroglutamine anhydride and .DELTA.1-dehydroglutaminyldipeptides.
• Dehydrooligopeptides. III. Synthesis of (Z,Z)- and (Z,E)-geometric isomers of dehydrodipeptides and their base-catalyzed transformation to the hydantoin derivatives.
• The confirmation of the configuration of ethyl 2-bromo-3-nitro-2-alkenoate by 13C NMR spectroscopy.
• Dehydrooligopeptides. VI Facile transformation of .ALPHA.-phosphoranylideneamino-.ALPHA.-alkenoates to .DELTA.2-dehydrodipeptide derivatives.
• Dehydrooligopeptides. VII Convenient synthesis of various dehydrodi- and tripeptide esters by using N-carboxy .ALPHA.-dehydroamino acid anhydride.
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XVII. The facile synthesis of ethyl .ALPHA.-azido-.ALPHA.-alkenoates and reduction to ethyl .ALPHA.-amino-.ALPHA.-alkenoates.
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XIV. The synthesis and reduction of Diels-Alder adducts from ethyl 3-nitro-2-alkenoates and cyclopentadiene.
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XV. The reaction of ethyl 3-nitro-2-alkenoate with bromine azide or bromine, and transformations of the products.
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XXI. A novel synthesis of .ALPHA.-dehydroamino acid derivatives by the Arbusov reaction of .ALPHA.-phosphoranylideneamino-2-alkenoates.
• Dehydrooligopeptides. II. The synthesis of dehydrodehydrodipeptides by direct coupling and base-catalyzed .BETA.-elimination.
• Convenient Synthesis of Dehydrooligopeptides by the Solid Phase Method Using N-Carboxy α-Dehydroamino Acid Anhydride
• A Novel Synthesis of Ethyl β-Diethoxyphosphinyl-α,β-unsaturated-carboxylates
• The formation of the main skelton of bicyclomycin by the cyclization of 6-hydroxy-3-(3-hydroxypropyl)-2,5-piperazinedione derivatives.
• The Synthesis and Reaction of α,β-Unsaturated α-Nitrocarboxylic Esters
• .ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XIX. The convenient synthesis of .ALPHA.-alkoxy-, .ALPHA.-hydroxy-.ALPHA.-amino acid, and its cyclic dipeptide from .ALPHA.-dehydroamino acid.
• Branched-Chain Sugars. II. On the Configuration of Branched-Chain Sugars from Methyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-ribo-hexopyranosid-3-ulose
• α,β-Unsaturated Carboxylic Acid Derivatives. X. The Synthesis and Reaction of α-Azido-diethoxyphosphinyl-α- and β-alkenes
• Studies on Nitro Carboxylic Acids. III. The Reaction of α-Nitroolefins with Triethyl or Diethyl Phosphite

もっと見る 閉じる

スポンサーリンク