Search results for "combinatorial"

showing 10 items of 1208 documents

ChemInform Abstract: Solution and Fluorous Phase Synthesis of β,β-Difluorinated 1-Amino-1-cyclopentane Carboxylic Acid Derivatives.

2009

An efficient protocol for the preparation of β,β-difluorinated 1-amino-1-cyclopentane carboxylic acid derivatives was developed. 2,2-Difluro-4-phenyl-3-butenoic acid 6 was used as substrate for the preparation of the starting vinyl difluoro imino esters 8. The key steps of this methodology rely on the chemo- and diastereoselective addition of allylzinc bromides over the iminic functionality of 8 and subsequent RCM reaction. This synthetic sequence was successfully applied to fluorous synthesis.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryCarboxylic acidSalt metathesis reactionSubstrate (chemistry)Organic chemistrySequence (biology)General MedicineCyclopentaneCombinatorial chemistryPhase synthesisChemInform
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Studies towards the development of lipophilic bifunctional N3S3 chelators for 68Ga

2010

Abstract The present study is concerned with a concept of charge-neutral, lipophilic, macrocyclic bifunctional chelators, suitable for the introduction of a gallium-68 label into small molecules. The synthesis of a novel bifunctional N3S3-type chelator, derived from 1,4,7-triazacyclononane, initial 68Ga-radiolabelling and the determination of stability and calculated lipophilicity of the compound are described. The 68Ga-labelled chelate was obtained in a maximum radiochemical yield of 93±5% after a reaction time of 2 min. It remained intact over 3 h in a DTPA-challenge and a transferrin challenge experiment, indicating sufficient stability for PET studies.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryTransferrinYield (chemistry)LipophilicityOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalCombinatorial chemistrySmall moleculeRadiochimica Acta
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Chemistry of Enzyme Visualization

1994

The basic principle of enzyme visualization in situ is to present an enzyme with a solution containing an enzyme specific substrate. Demonstration of an enzyme is achieved if the catalytic action of the enzyme on this substrate produces a coloured reaction product. Often, however, the primary reaction products are colourless and require coupling with a visualizing agent to generate a coloured, preferably insoluble, final reaction product.

chemistry.chemical_classificationchemistry.chemical_compoundEnzymePrimary reactiongenetic structuresChemistrySubstrate specificitySubstrate (chemistry)FormazanCombinatorial chemistryReaction productVisualizationCatalysis
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Advances in N ‐ and O ‐Glycopeptide Synthesis – A Tool to Study Glycosylation and Develop New Therapeutics

2011

chemistry.chemical_classificationchemistry.chemical_compoundGlycosylationChemistryGlycobiologyGlycoproteinCombinatorial chemistryGlycopeptideAmino Acids, Peptides and Proteins in Organic Chemistry
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Electrochemical production of initiators for polymerization processes

2007

The most important technological interest in initiator production lies, in the electrosynthesis of complex catalytic systems, i. e. coordination compounds and Ziegler-Natta catalysts, although the choice of olefins to be polymerized with these electrosynthesized complexes is still limited to ethylene and to very few other monomers.

chemistry.chemical_classificationchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationCationic polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationElectrosynthesisCombinatorial chemistryCoordination complex
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Structure and properties of pharmacologically active polymers

1975

Although the concept of using pharmacologically active macromolecular compounds as drugs is still regarded with much skepticism for both theoretical and practical reasons, interest in this field has grown in recent years because of the opportunity to take advantage of the specific properties of polymeric materials. For low molecular weight drugs, changes in structure often lead to a loss of specific activity. On the other hand, the properties of macromolecular drugs depend on the structure of the polymer used and this can be varied over a wide range by the incorporation of comonomer units, by the application of polymer-analogous reactions, or by related structural changes. A new model is pr…

chemistry.chemical_classificationchemistry.chemical_compoundPolymer-drug conjugateschemistryMacromolecular prodrugsComonomerGeneral EngineeringOrganic chemistryBiological activityPolymerMacromolecular CompoundsCombinatorial chemistryMacromoleculeJournal of Polymer Science: Polymer Symposia
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Carbohydrates as Polyfunctional Scaffolds in Combinatorial Synthesis

2006

Carbohydrates are inexpensive, polyfunctional molecules which contain a high density of stereogenic centers. Taking advantage of these particular properties monosaccharides like glucose or mannose have been used for the construction of peptidomimetics which simulate recognition sites of somatostatin or RGD ligands of integrins. Due to their poly functionality, carbohydrates are considered promising scaffolds for combinatorial syntheses either in solution or on solid phase. The application of carbohydrate scaffolds, however, requires sets of orthogonally stable, selectively removable protecting groups, and the challenge in this combinatorial strategy increases with increasing number of hydro…

chemistry.chemical_classificationchemistry.chemical_compoundSolid-phase synthesischemistryPeptidomimeticMonosaccharideMannoseSequence (biology)General MedicineCarbohydrateCombinatorial chemistryLinkerStereocenterChemInform
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Experimental and Theoretical MEDT Study of the Thermal [3+2] Cycloaddition Reactions of Aryl Azides with Alkyne Derivatives

2018

chemistry.chemical_classificationchemistry.chemical_compoundchemistry010405 organic chemistryArylAlkyneRegioselectivityGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical sciencesChemistrySelect
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ChemInform Abstract: A Catalyst Designed for the Enantioselective Construction of Methyl- and Alkyl-Substituted Tertiary Stereocenters.

2016

Tertiary methyl-substituted stereocenters are present in numerous biologically active natural products. Reported herein is a catalytic enantioselective method for accessing these chiral building blocks using the Mukaiyama-Michael reaction between silyl ketene thioacetals and acrolein. To enable remote enantioface control on the nucleophile, a new iminium catalyst, optimized by three-parameter tuning and by identifying substituent effects on enantioselectivity, was designed. The catalytic process allows rapid access to chiral thioesters, amides, aldehydes, and ketones bearing an α-methyl stereocenter with excellent enantioselectivities, and allowed rapid access to the C4-C13 segment of (-)-b…

chemistry.chemical_classificationchemistry.chemical_compoundchemistryNucleophileOrganocatalysisEnantioselective synthesisSubstituentKeteneIminiumGeneral MedicineCombinatorial chemistryAlkylStereocenterChemInform
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Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles.

2019

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5 -mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

chemistry.chemical_classificationcyclization010405 organic chemistryChemistryoxidationOrganic ChemistryHalideGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reactionC−H activationsulfur heterocycles0104 chemical sciencesDiselenidemolybdenumAtom economyIntramolecular forceElectrophileStructural motifAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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