SHIN Chung-gi | Laboratory of Organic Chemistry, Faculty of Technology, Kanagawa University

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
Total Synthesis of Bistratamides G and H from Various Kinds of ΔAla and ΔAbu-Containing Oligopeptides
Convenient Synthesis of the Main Dehydrohexapeptide Skeleton Constituting a Macrocyclic Antibiotic, Berninamycin A
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
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
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
Synthesis of (3Z, 6E)-1-N-Methylalbonoursin, a New Metabolite from Streptomyces albus
.ALPHA.,.BETA.-Unsaturated carboxylic acid derivatives. XXI. A novel synthesis of .ALPHA.-dehydroamino acid derivatives by the Arbusov reaction of .ALPHA.-phosphoranylideneamino-2-alkenoates.

もっと見る

スポンサーリンク