Search results for "Esterification"

showing 10 items of 71 documents

A novel phosphorus–carbon bond formation by ring opening with diethyl phosphite of oxazolines derived from serine

2004

Abstract A new reaction of oxazolines derived from serine with diethyl phosphite leading to ring opening products with P–C bond formation is reported. This reaction, which proceeds under neutral conditions and without the use of any halogenated intermediate, results in a mixture of racemic α- and β-phosphono alanines in an approximate 1:2 ratio, with isolated yields up to 77%. The mechanism involves the rearrangement of the oxazoline into the corresponding α-benzamido acrylate, followed by addition of the diethyl phosphite to the double bond. Since no significant transesterification is observed, this method constitutes a simple route for α- and β-phosphono amino acids bearing suitable prote…

chemistry.chemical_classificationAcrylateDouble bondOrganic Chemistrychemistry.chemical_elementOxazolineTransesterificationRing (chemistry)BiochemistryMedicinal chemistryAmino acidSerinechemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCarbonTetrahedron
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DUAL APPLICATION OF DIVALENT ION-ANCHORED CATALYST: BIODIESEL SYNTHESIS AND PHOTOCATALYTIC DEGRADATION OF CARBAMAZEPINE

2019

chemistry.chemical_classificationBiodieselfood.ingredientfoodchemistryLinseed oilChemical engineeringGeneral MedicineTransesterificationPhotocatalytic degradationDivalentCatalysisIonCatalysis in Green Chemistry and Engineering
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Improving lipase activity in solvent-free media by interfacial activation-based molecular bioimprinting

1997

Abstract Nine lipases of mammalian, fungal and bacterial origin and two different model reactions, direct esterification and transesterification (alcoholysis), have been used to probe the potential in solvent-free media of the recently reported strategy of interfacial activation-based molecular (bio)imprinting (IAMI) [Mingarro et al., Proc. Natl. Acad. Sci. USA , 92 (1995) 3308]. The results demonstrate that the imprinting treatment permits nonaqueous rate accelerations which are lipase-dependent and span in some cases up to higher than two orders of magnitude. For several lipases, the method allows conversion yields after short reaction times (in either of the model reactions assayed) whic…

chemistry.chemical_classificationCarboxylic Ester HydrolasesSolvent freebiologyChemistryProcess Chemistry and TechnologyTriacylglycerol lipaseBioengineeringTransesterificationBiochemistryCatalysisInorganic saltsEnzymebiology.proteinOrganic chemistryLipaseJournal of Molecular Catalysis B: Enzymatic
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Neutron Scattering of Poly(ethylene terephthalate)

1986

Through the use of deuterium labeling, small angle neutron scattering (SANS) has been found to be an extremely effective tool for elucidating the structure of polymer molecules in the condensed matter state. In this study, the molecular morphology of poly(ethylene terephthalate) (PET) has been determined under four different conditions: (1) in the glassy state, (2) in the semicrystalline state, (3) after cold-drawing, and (4) after undergoing partial transesterification.

chemistry.chemical_classificationCrystallinityDimethyl terephthalatechemistry.chemical_compoundMaterials scienceEthyleneDeuteriumchemistryPhysical chemistryTransesterificationPolymerNeutron scatteringSmall-angle neutron scattering
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The Catalytic Mechanism of Carboxylesterases: A Computational Study

2014

The catalytic mechanism of carboxylesterases (CEs, EC 3.1.1.1) is explored by computational means. CEs hydrolyze ester, amide, and carbamate bonds found in xenobiotics and endobiotics. They can also perform transesterification, a reaction important, for instance, in cholesterol homeostasis. The catalytic mechanisms with three different substrates (ester, thioester, and amide) have been established at the M06-2X/6-311++G**//B3LYP/6-31G* level of theory. It was found that the reactions proceed through a mechanism involving four steps instead of two as is generally proposed: (i) nucleophilic attack of serine to the substrate, forming the first tetrahedral intermediate, (ii) formation of the ac…

chemistry.chemical_classificationEsterificationStereochemistrycomputational studiesHydrolysisSubstrate (chemistry)AlcoholTransesterificationcatalytic mechanismCrystallography X-RayThioesterBiochemistryCatalysischemistry.chemical_compoundcarboxylesterasesNucleophilechemistryhydrolysisTetrahedral carbonyl addition compoundAmideBiocatalysisCarboxylic Ester Hydrolases
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Synthesis of dehydrodipeptide esters and their evaluation as inhibitors of cathepsin C

2015

The procedures for the synthesis of esters of dehydropeptides containing C-terminal (Z)-dehydrophenylalanine and dehydroalanine have been elaborated. These esters appeared to be moderate or weak inhibitors of cathepsin C, with some of them exhibiting slow-binding behavior. As shown by molecular modeling, they are rather bound at the surface of the enzyme and are not submersed in its binding cavities. Electronic supplementary material The online version of this article (doi:10.1007/s00044-015-1366-0) contains supplementary material, which is available to authorized users.

chemistry.chemical_classificationMolecular modelmolecular modelingesterificationenzyme inhibitorsPharmacology toxicologyOrganic ChemistryhumanitiesCathepsin Cchemistry.chemical_compoundPharmacology Toxicology and Pharmaceutics(all)EnzymedehydropeptideschemistryBiochemistryDehydroalanineGeneral Pharmacology Toxicology and PharmaceuticsOriginal ResearchMedicinal Chemistry Research
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On the structure of passifloricin A: asymmetric synthesis of the delta-lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)tetrahydroxyhexacos-2-enoi…

2003

Stereoselective syntheses of the delta-lactone of (2Z,5S,7R,9S,11S)-tetrahydroxyhexacos-2-enoic acid, the structure reported for passifloricin A, and of its (5R)-epimer are described. The creation of all stereogenic centers relied upon Brown's asymmetric allylation methodology. The lactone ring was created via ring-closing metathesis. The NMR data of both synthetic products, however, were different from those of the natural product. The published structure of passifloricin A is thus erroneous and will require further synthetic work to be unambiguously assigned. [structure: see text]

chemistry.chemical_classificationNatural productEsterificationChemistryStereochemistryOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismRing (chemistry)MetathesisBiochemistryStereocenterFatty Acids Monounsaturatedchemistry.chemical_compoundLactonesCyclizationPyronesStereoselectivityPhysical and Theoretical ChemistryLactoneOrganic letters
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Selective Formal Transesterification of Fluorinated 2-(Trimethylsilyl)ethyl α-Imino Esters Mediated by TBAF

2008

The scope of the transesterification reaction between beta-fluorinated alpha-imino esters and various electrophiles in the presence of TBAF as fluorine source is described. The reaction is highly selective for alkyl iodides, bromides, and mesylates, while alkyl chlorides react at a significantly slower rate and tosylates do not react under the reaction conditions. This methodology represents a simple and useful alternative for the preparation of a wide variety of fluorinated alpha-imino esters.

chemistry.chemical_classificationTrimethylsilylChemistryOrganic Chemistrychemistry.chemical_elementTransesterificationChemical synthesisReaction ratechemistry.chemical_compoundElectrophileFluorineOrganic chemistryheterocyclic compoundsSelectivityAlkylThe Journal of Organic Chemistry
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1978

Synthesis and characterization of polymeric derivatives of the folic acid antagonist, Methotrexate, N-[4-(N-methyl-2,4-diamino-6-pteridinylmethylamino)benzoyl] glutamic acid (1a), a widely used antitumor agent, are described. Derivatives of poly(L-lysine), poly(iminoethylene), poly(vinyl alcohol), and carboxymethylcellulose with various contents (3–15 mole-%) of substituted repeating units were prepared by polymer-analogous amidation and transesterification of the dimethyl ester of 1a and with N-[2-(N-methylmorpholinio)ethyl]carbodiimide p-toluenesulfonate as coupling reagent. By nucleophilic addition reactions of the pteridinyl amino groups under mild conditions, 1a was bound without cross…

chemistry.chemical_classificationVinyl alcoholchemistry.chemical_compoundResidue (chemistry)Nucleophilic additionMembranechemistryPolymer chemistryCopolymerOrganic chemistryTransesterificationPolymerCarbodiimideDie Makromolekulare Chemie
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Water-Blown Polyisocyanurate Foams From Vegetable Oil Polyols

2008

Polyols with the hydroxyl value OHV from 290 to 318 mg KOH/g are synthesized from rapeseed, sunflower seed, flaxseed, or coconut oils by the way of their: (1) transesterification with triethanolamine or (2) amidization with diethanolamine. The influence of water as the blowing agent on the storage stability of the polyol premix system is assessed from values of the polyol premix system pH, acid value, and variations in such parameters as cream and gel time. Water-blown polyisocyanurate (PIR) foams (150 · II × 300; II—isocyanate index) characterized by good mechanical characteristics, dimensional stability at 70°C and at relative humidity RH = 95% as well as by a very low water absorbance, …

chemistry.chemical_classificationbusiness.product_categoryMaterials scienceRapeseedPolymers and PlasticsPolyisocyanurateGeneral ChemistryTransesterificationVegetable oilPolyolchemistryBlowing agentHydroxyl valueMaterials ChemistryOrganic chemistrySunflower seedbusinessJournal of Cellular Plastics
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