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Bonds synthesis

Nissen P, Hansen J, Ban N et al (2000) The structural basis of ribosome activity in peptide bond synthesis. Science 289 920-930... [Pg.1090]

Formation of glutamine is catalyzed by mitochondrial glutamine synthase (Figure 29-7). Since amide bond synthesis is coupled to the hydrolysis of ATP to ADP and P , the reaction strongly favors glutamine synthesis. One function of glutamine is to sequester ammonia in a nontoxic form. [Pg.245]

Oinuma K-I, Y Hashimoto, K Konishi, M Goda, T Noguchi, H Higashibata, M Kobayashi (2003) Novel aldox-ime dehydratase involved in carbon-nitrogen triple bond synthesis of Pseudomonas chlororaphis B23. J Biol Chem 278 29600-29608. [Pg.143]

Peptide bond synthesis Protein synthesis (on ribosomes) ATP, GTP... [Pg.201]

The chemistry of a-haloketones, a-haloaldehydes and a-haloimines Nitrones, nitronates and nitroxides Crown ethers and analogs Cyclopropane derived reactive intermediates Synthesis of carboxylic acids, esters and their derivatives The silicon-heteroatom bond Synthesis of lactones and lactams Syntheses of sulphones, sulphoxides and cyclic sulphides Patai s 1992 guide to the chemistry of functional groups—Saul Patai... [Pg.1192]

It is interesting to note that serine peptidases can, under special conditions in vitro, catalyze the reverse reaction, namely the formation of a peptide bond (Fig. 3.4). The overall mechanism of peptide-bond synthesis by peptidases is represented by the reverse sequence f-a in Fig. 3.3. The nucleophilic amino group of an amino acid residue competes with H20 and reacts with the acyl-enzyme intermediate to form a new peptide bond (Steps d-c in Fig. 3.3). This mechanism is not relevant to the in vivo biosynthesis of proteins but has proved useful for preparative peptide synthesis in vitro [17]. An interesting application of the peptidase-catalyzed peptide synthesis is the enzymatic conversion of porcine insulin to human insulin [18][19]. [Pg.69]

Fig. 3.3. Major steps in the hydrolase-catalyzed hydrolysis of peptide bonds, taking chymo-trypsin, a serine hydrolase, as the example. Asp102, His57, and Ser195 represent the catalytic triad the NH groups of Ser195 and Gly193 form the oxyanion hole . Steps a-c acylation Steps d-f deacylation. A possible mechanism for peptide bond synthesis by peptidases is represented by the reverse sequence Steps f-a. Fig. 3.3. Major steps in the hydrolase-catalyzed hydrolysis of peptide bonds, taking chymo-trypsin, a serine hydrolase, as the example. Asp102, His57, and Ser195 represent the catalytic triad the NH groups of Ser195 and Gly193 form the oxyanion hole . Steps a-c acylation Steps d-f deacylation. A possible mechanism for peptide bond synthesis by peptidases is represented by the reverse sequence Steps f-a.
The enzymatic reaction chosen for the DCL was protease-catalyzed amide bond synthesis/hydrolysis. This fundamental transformation is... [Pg.67]

What is not included here is the need also to protect any vulnerable functional groups in the amino acid side-chains. A range of methods is available to protect amino, carboxyl, thiol, and hydroxyl groups and prevent them reacting during the amide bond synthesis. Such groups also have to be removed after their job is done, using conditions that do not... [Pg.540]

A very interesting report was published on the self-assembly of polyoxometallate elusters into a 3-D heterometallie framework via eovalent bonding synthesis, strueture and eharaeterization of... [Pg.45]

Nelson RJ, Ziegelhoffer T, Nicolet C, Werner-Washburne M, Craig EA (1992) The translation machinery and 70 kd heat shock protein cooperate in protein synthesis. Cell 71 97-105 Nissen P, Hansen J, Ban N, Moore PB, Steitz TA (2000) The structural basis of ribosome activity in peptide bond synthesis. Science 289 920-930... [Pg.27]

Moissan and his colleague Meslans then tried other methods for C —F bond synthesis.121 Alkyl fluorides could not be made via reactions of alcohols with hydrogen fluoride or phosphorus fluorides. However, silvcr(l) fluoride was found to function as a halogen-exchange reagent and several alkyl fluorides were made and characterized, all being fairly resistant to alkaline hydrolysis. [Pg.4]

This chapter, which is based on the literature that had appeared through the end of 1983, surveys the coordination chemistry of the element with special emphasis on structure, bonding, synthesis and chemical behavior. The discussion is limited to well-characterized complexes and well-understood systems. [Pg.974]

H. Kunz and C. Unverzagt, Protecting group-dependent stability of intersaccharide bonds— synthesis of a fucosyl-chitobiose glycopeptide, Angew. Chem. lnt. Ed. Engl. 27 1697 (1988). [Pg.281]

However, ester bond synthesis in aqueous conditions has been reported, but low yields were obtained. [Pg.93]

The Chemistry of N-C02 Bonds Synthesis of Carbamic Acids and Their Derivatives, Isocyanates, and Ureas... [Pg.121]

Sukumaran J, Hanefeld U (2005) Enantioselective C-C bond synthesis catalysed by enzymes. Chem Soc Rev 34 530-542... [Pg.37]

Kunz, H. and Unverzagt, C. (1988) Protecting-group-dependant stability of intersaccharide bonds-Synthesis of a fucosyl-chitobiose glycopeptide. Angew. Chem. Int. Ed. 27, 1697-1699. [Pg.208]

This type of metal carbonyl derivative has lately been the object of numerous investigations by many research groups with particular reference to metal-metal bond synthesis.3 In our laboratory the nitrosyl carbonyliron compounds R3MFe(NO)(CO)3 (M = Si, Ge, Sn, Pb R= C6H5, C4H9) have been prepared, and shown by infrared studies to have a trigonal bipyramidal structure with Cs symmetry (48). [Pg.11]

A 4-bond synthesis of pyridines from carbonyl compounds, which were subjected to Vilsmeier-Haack conditions giving the conjugated iminium salts, has been achieved by reaction with ammonium acetate (Scheme 113)... [Pg.289]

In this section, acid-catalysed glycosidic bond synthesis and cleavage will be covered. This knowledge is critical to many discussions that will follow in subsequent chapters. In Chapter 4, modern approaches to the introduction of glycosidic linkages are discussed. [Pg.19]

Figure 4.1 Glycosyl donors for glycosidic bond synthesis. Figure 4.1 Glycosyl donors for glycosidic bond synthesis.

See other pages where Bonds synthesis is mentioned: [Pg.289]    [Pg.179]    [Pg.59]    [Pg.2]    [Pg.14]    [Pg.120]    [Pg.492]    [Pg.36]    [Pg.240]    [Pg.33]    [Pg.289]    [Pg.109]    [Pg.1]    [Pg.1061]    [Pg.649]    [Pg.155]    [Pg.859]    [Pg.71]    [Pg.350]    [Pg.362]    [Pg.103]    [Pg.103]   
See also in sourсe #XX -- [ Pg.2 , Pg.8 , Pg.57 , Pg.708 ]




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Antimony-arsenic bonds synthesis

Antimony—phosphorus bonds synthesis

Armed-Disarmed Concept in the Synthesis of Glycosidic Bond

Arsenic—phosphorus bonds synthesis

Aryl ether synthesis, carbon-oxygen bond formation

Bond dissociation energies synthesis

Bond formation synthesis Substitution reactions

C bonds formation synthesis

Carbon Bonding-Forming Reactions in Organic Synthesis

Carbon-nitrogen bonds oxidation synthesis

Carbon-oxygen bonds aryl ether synthesis

Carbon-oxygen bonds oxidation synthesis

Carbon-oxygen double bonds stereoselective synthesis

Carbon-palladium bonds stoichiometric synthesis

Carbon-sulfur bond formation synthesis

Carbon—arsenic bond, synthesis

Carbon—hydrogen bonds metal carbene synthesis

Chemical glycosidic bond synthesis

Chlorine bond synthesis

Covalent-bond synthesis

Cr-bond complexes synthesis

Diastereoselective synthesis carbon-hydrogen bond activation

Diene synthesis double bonds

Dienes heterocyclic synthesis, double bonds

Disulfide-bonded proteins, synthesis

Double bond formation synthesis

Double bonds diastereoselective synthesis

Double bonds heterocyclic synthesis

Double bonds multistep synthesis

Double bonds natural product synthesis

Ester-bond synthesis

Glycopeptide bond synthesis

Glycopeptide bond synthesis involved

Hybrid materials synthesis covalent bonding

Hydrogen Bond Catalysis in Total Synthesis

Hydrogen Bonding in Organic Synthesis. Edited by Petri M. Pihko

Hydrogen Bonding-assisted Syntheses

Hydrogen bonding amide based synthesis

Hydrogen bonding template synthesis

Hydrogen-bonded assemblies, noncovalent synthesis

Metal—carbon triple bonds synthesis

Multiple Bond Formation Synthesis of Sodium Azide

Natural products synthesis double bond migration

Nitrogen-phosphorus bonds synthesis

Organosilicon synthesis silicon—carbon bond formation

PSiP Transition-Metal Pincer Complexes Synthesis, Bond Activation, and Catalysis

Peptide bonds synthesis

Polypeptide synthesis, bond, chain, initiation, elongation

Protein synthesis peptide bond

Rhodium-Catalyzed Vinyldiazoesters Insertion Into Si—H Bonds. Synthesis of Allylsilanes

Ring Syntheses Involving Formation of Two Bonds Fragments

Ruthenium-Catalyzed Synthesis of Heterocycles via C-H Bond Activation

Silicon bond synthesis

Silicon-carbon bond synthesis

Silicon-hydrogen bond synthesis

Silicon-nitrogen bond synthesis

Silicon-oxygen bond synthesis

Solids, supramolecular synthesis hydrogen bonding

Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis, First Edition

Stereoselective synthesis multiple bond additions

Stereoselective synthesis single bond additions

Stoichiometric synthesis bonds

Syntheses via C-H Bond Functionalizations

Synthesis Involving Formation of Three or More Bonds

Synthesis Involving Formation of Two Bonds

Synthesis and Reactivity of Ln-C Bonds

Synthesis and Reactivity of Ln-H Bonds

Synthesis and Self-Assembly of Hydrogen-Bonded Supramolecular Polymers

Synthesis of Alkylamines and Related Compounds through Nitrogen-Carbon(sp3) Bond-Forming Reactions

Synthesis of Amide Bonds

Synthesis of Carbazoles and Related Compounds via C—E Bond-Forming Coupling Reactions

Synthesis of Heterocycles via X—H Bond Addition to Diynes

Synthesis of Macromonomers with a Polymerizable Double Bond

Synthesis of Naproxen and Ibuprofen (by C-H Bond Formation)

Synthesis of Pyridazines via Two Bond Formation

Synthesis of Vegetable Oil Polyols by using Reactions Involving the Double Bonds

Synthesis of Ynamides and Related Compounds through Nitrogen-Carbon(sp) Bond-Forming Reactions

Synthesis of bonded phase materials

Synthesis strategic bond approach

Synthesis unsaturated bonds

Synthesis, Structure and Bonding in Fischer Carbenes

Synthesis, Structure and Bonding in Schrock Carbenes

Total synthesis polar double bonds

Transition metal-germanium double bond synthesis

Transition metal-germanium single bond synthesis

Transition metal-germanium triple bond synthesis

Transition metal-lead double bond synthesis

Transition metal-lead single bond synthesis

Typical Ring Synthesis of a Pyridine Involving Only C-Heteroatom Bond Formation

Typical Ring Synthesis of a Pyrrole Involving Only C-Heteroatom Bond Formation

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