Yang et al., 1986 - Google Patents
Effects of solvents and additives on the reaction of N-(benzyloxycarbonyl)-L-aspartic anhydride with L-phenylalanine methyl ester (synthesis of aspartame)Yang et al., 1986
- Document ID
- 15688434237730448618
- Author
- Yang C
- Su C
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
IV-Benzyloxycarbonyl-L-aspartic anhydride (ZL-aspartic anhydride) was reacted with L- phenylalanine methyl ester. The nature of the ring-opening reaction was affected by the organic solvent. In Me2SO, DMF, and dimethylacetamide the/3-isomer of ZL-aspartyl-L …
- 238000006243 chemical reaction 0 title abstract description 47
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
- C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Yang et al. | Effects of solvents and additives on the reaction of N-(benzyloxycarbonyl)-L-aspartic anhydride with L-phenylalanine methyl ester (synthesis of aspartame) | |
HU217612B (en) | Process for producing peptides of elastaze- and cathepsin-g-inhibitor activity | |
WO2001047949A1 (en) | Aspartame derivative crystals | |
US3814732A (en) | Modified solid supports for solid phase synthesis | |
JPS61267600A (en) | Production of n-protected-alpha-l-aspartyl-l-phenylalaninemethyl ester | |
IE42785B1 (en) | L-3-(3,4-dihydroxyphenyl)-2-methyl-alanine peptides | |
JI et al. | Cyclization studies with a model pentapeptide | |
US4309341A (en) | Method for purifying α- L-aspartyl-L-phenylalanine lower alkyl ester | |
IE50856B1 (en) | Method of producing n-benzyloxycarbonyl-l-aspartic acid | |
Ariyoshi et al. | The synthesis of a sweet peptide, α-l-aspartyl-l-phenylalanine methyl ester, without the use of protecting groups | |
McGahren et al. | Carbon-13 nuclear magnetic resonance studies on a new antitubercular peptide antibiotic LL-BM547. beta. | |
US3891692A (en) | N-(cyclopropylalkoxycarbonyl)amino acids | |
Guarnaccia et al. | Co‐oligopeptides of aromatic amino acids and glycine with a variable distance between the aromatic residues. I. Synthesis of co‐oligopeptides of tryptophan and glycine | |
JP2662287B2 (en) | Method for separating α-L-aspartyl-L-phenylalanine methyl ester | |
JP3888402B2 (en) | Process for producing optically active N-carbobenzoxy-tert-leucine | |
EP0102483A1 (en) | Process for preparing alpha-l-aspartyl-l-phenylalanine alkyl esters | |
JPS58177951A (en) | Chromogenic peptide and manufacture | |
JPH0245640B2 (en) | ||
CN112830957B (en) | Method for preparing carfilzomib | |
DK147622B (en) | PROCEDURE FOR CLEANING A L-ASPARTYL-L-PHENYLALANINE ALKYL ESTER FOR SMELLING POLLUTANTS | |
Dubois et al. | Vitamin K dependent carboxylation: synthesis and biological properties of tetrazolyl analogs of pentapeptidic substrates | |
CN113024637A (en) | Method for preparing carfilzomib by using water-soluble alkynylamide as condensing agent | |
JP2647420B2 (en) | Method for producing N-protected-α-L-aspartyl-L-phenylalanine methyl ester | |
JP2647439B2 (en) | Method for producing N-protected-α-L-aspartyl-L-phenylalanine methyl ester | |
JPH04346996A (en) | Production of n-formyl-alpha-l-aspartyl-l-phenylalanine |