Peptide Synthesis by Oxidation-Reduction Condensation. II. The Use of Disulfide as an Oxidant
スポンサーリンク
概要
- 論文の詳細を見る
A peptide synthesis starting from free <I>N</I>-protected amino acid and free amino acid ester by the use of triphenylphosphine, an oxygen acceptor, and disulfide, a hydrogen acceptor, was studied. The oxidation-reduction condensation reaction affords peptides with high optical purity in excellent yields by simple procedure.
- 公益社団法人 日本化学会の論文
著者
-
Mukaiyama Teruaki
Laboratory of Organic Chemistry Tokyo Institute of Technology
-
Matsueda Rei
Laboratory of Organic Chemistry, Tokyo Institute of Technology
-
Maruyama Hiroshi
Laboratory of Organic Chemistry, Tokyo Institute of Technology
-
Ueki Masaaki
Laboratory of Organic Chemistry, Tokyo Institute of Technology
関連論文
- Dehydration Reactions of Benzaldoxime by Means of Compounds Having a Nitrogen-Carbon Double Bond
- Pyrolysis of Acid Amides. III. Pyrolysis of Cyanoacetamides and 2-Phenylacetamides
- A Selective Phosphorylation by Means of α-Bromocyano acetamides and Trialkyl Phosphites
- Synthesis of Testosterone Dimethyl Phosphate, Bornyl Phosphate and Adenosine 5′-Phosphate
- Solid Phase Peptide Synthesis by Oxidation-Reduction Condensation. Synthesis of LH–RH by Fragment Condensation on Solid Support
- A Convenient Method for the Preparation of Thiolesters
- Peptide Synthesis by Oxidation-Reduction Condensation. II. The Use of Disulfide as an Oxidant
- Ring Expansion through a 1,3-Acyl Rearrangement. Reactions of Cyclic Sulfonium Ylides with Acetylenic Compounds
- A Convenient Method for Hydrolysis of 1,3-Dithiane Derivatives Using Cupric Chloride
- The Reactions of Complexes of Thioboronite with Compounds Containing Carbon-Nitrogen Multiple Bond
- Syntheses of Acylurea Derivatives as Model Compounds for a Highly Specific Organic Reaction
- Reactions of Vinyloxyboranes. A Convenient Method for the Preparation of β-Hydroxy Thiolesters, Esters and Ketones
- The Reactions of Phosphonium Ylides and Oxosulfonium Methylide with Sulfenamide Derivatives
- The Reactions of β-Ketosulfonium Salts with Sulfenamide Derivatives
- Reactions of Sulfonium and Pyridinium Salts with Alkyl Nitrite
- A Convenient Method for the Preparation of Ketones by the Reaction of Grignard Reagents with Carboxylic Acid Derivatives
- Syntheses and Reactions of 2-Ethylthio- or 2-Phenylthio-2-cycloalkenones
- The Reactions of α-Substituted Carbonyl-stabilized Sulfonium Ylides with Succinic Anhydride
- A Convenient Method for the Hydrolysis of Vinyl Sulfides to Ketones
- The Activation of Bivalent Sulfur Compounds with Cupric Chloride and Zinc Chloride. The Benzylation and Acylation of Aromatic Compounds with Sulfides and Thiol Esters
- Sulfenylation of Active Methylene Compounds with Sulfenamides
- A convenient synthesis of .BETA.-acetyl-.GAMMA.-substituted-.GAMMA.-butyrolactones and .GAMMA.-acetyl-.DELTA.-substituted-.DELTA.-valerolactones.
- Peptide Synthesis by Oxidation-Reduction Condensation. I. Use of NPS-Peptides as Amino Component
- Phosphorylation by Oxidation-Reduction Condensation. Preparation of Active Phosphorylating Reagents
- Peptide Synthesis via Oxidation-Reduction Condensation by the Use of Non-metallic Compound as a Mercaptan Scavenger