[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Katritzky et al., 2007 - Google Patents

Microwave‐assisted solid‐phase peptide synthesis utilizing N‐Fmoc‐protected (α‐aminoacyl) benzotriazoles

Katritzky et al., 2007

View PDF
Document ID
3166074308583026177
Author
Katritzky A
Khashab N
Yoshioka M
Haase D
Wilson K
Johnson J
Chung A
Haskell‐Luevano C
Publication year
Publication venue
Chemical Biology & Drug Design

External Links

Snippet

Microwave‐Assisted Solid‐Phase Peptide Synthesis Utilizing N‐Fmoc‐Protected (α‐aminoacyl)benzotriazoles - Katritzky - 2007 - Chemical Biology & Drug Design - Wiley Online Library Skip to Article Content Skip to Article Information Wiley Online Library Wiley Online Library Search within …
Continue reading at www.academia.edu (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1027Tetrapeptides containing heteroatoms different from O, S, or N
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/12General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/04General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04Linear peptides containing only normal peptide links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06General 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
    • C07K1/061General 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

Similar Documents

Publication Publication Date Title
Bai et al. Backbone‐Enabled Directional Peptide Macrocyclization through Late‐Stage Palladium‐Catalyzed δ‐C (sp2)− H Olefination
Huang et al. Chemical synthesis of proteins using hydrazide intermediates
Barrett et al. Amino acids and peptides
Sewald et al. Peptides: chemistry and biology
Kimmerlin et al. ‘100 years of peptide synthesis’: ligation methods for peptide and protein synthesis with applications to β‐peptide assemblies
Camarero et al. Fmoc-based synthesis of peptide α-thioesters using an aryl hydrazine support
Botti et al. Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation
Offer Native chemical ligation with Nα acyl transfer auxiliaries
Vanier Microwave-assisted solid-phase peptide synthesis based on the Fmoc protecting group strategy (CEM)
Meledin et al. Protein ubiquitination via dehydroalanine: development and insights into the diastereoselective 1, 4-addition step
Pires et al. Some mechanistic aspects on Fmoc solid phase peptide synthesis
Jensen Solid-phase peptide synthesis: an introduction
Katritzky et al. Microwave‐assisted solid‐phase peptide synthesis utilizing N‐Fmoc‐protected (α‐aminoacyl) benzotriazoles
De Filippis et al. Incorporation of the fluorescent amino acid 7‐azatryptophan into the core domain 1–47 of hirudin as a probe of hirudin folding and thrombin recognition
Khatri et al. Convenient synthesis of thioamidated peptides and proteins
Kawakami et al. Synthesis of histone proteins by CPE ligation using a recombinant peptide as the C-terminal building block
Ye et al. DEPBT as an efficient coupling reagent for amide bond formation with remarkable resistance to racemization
Loffredo et al. Microwave‐assisted solid‐phase peptide synthesis at 60° C: alternative conditions with low enantiomerization
Katritzky et al. Chiral acylation with N-(protected α-aminoacyl) benzotriazoles for advantageous syntheses of peptides and peptide conjugates
Gadais et al. Tailored Approaches towards the Synthesis of l‐S‐(Trifluoromethyl) cysteine‐and l‐Trifluoromethionine‐Containing Peptides
Flemer Jr Efficient method of circumventing insolubility problems with fully protected peptide carboxylates via in situ direct thioesterification reactions
Kwon et al. Encoded combinatorial libraries for the construction of cyclic peptoid microarrays
Katritzky et al. Benzotriazole-Assisted Solid-Phase Assembly of Leu-Enkephalin, Amyloid β segment 34− 42, and other “Difficult” Peptide Sequences
Pardo et al. Efficient Photochemical Synthesis of Peptide‐α‐Phenylthioesters
Teruya et al. Epimerization in peptide thioester condensation