Search results for "Isomer"

showing 10 items of 1308 documents

Conformational properties of N-acetyl-N-methyl-alpha,beta-dehydroalanine N'-methylamide.

2006

The conformational properties of Ac-Delta(Me)Ala-NHMe (N-acetyl-N-methyl-alpha,beta-dehydroalanine N'-methylamide), as the simplest model of N-methyl-alpha,beta-dehydroamino acids, was examined with theoretical methods and in comparison with Ac-DeltaAla-NHMe and Ac-DeltaAla-NMe(2). The N-terminal amide of the Delta(Me)Ala residue easily adopts the configuration cis and the torsion angles phi, psi are highly flexible. The Delta(Me)Ala residue is a conformational flexibilizer as compared to the parent DeltaAla, which is a conformational stiffener. This seems to be the reason why Delta(Me)Ala is found in small natural cyclic peptides, where it ensures the conformational flexibility necessary f…

chemistry.chemical_classificationModels MolecularAlanineMolecular StructureStereochemistryBiophysicsMolecular ConformationHydrogen BondingMethylamideAmidesGeneral Biochemistry Genetics and Molecular BiologyCis trans isomerizationCyclic peptidechemistry.chemical_compoundResidue (chemistry)chemistryModels ChemicalDehydroalanineAmideTheoretical methodsPeptidesActa biochimica Polonica
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Stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A.

2010

A stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A has been performed. The preparation of a cis-2,6-disubstituted tetrahydropyran ring via stereoselective reduction of an intermediate cyclic hemiacetal was one key feature of the synthesis. The macrocyclic lactone ring was created by means of a ring-closing metathesis (RCM), whereby the new C=C bond displayed exclusively the undesired Z configuration. Conversion to the required E configuration was achieved via photochemical isomerization.

chemistry.chemical_classificationModels MolecularCyclic compoundMagnetic Resonance SpectroscopyLightStereochemistryPhotochemistryOrganic ChemistryStereoisomerismStereoisomerismTetrahydropyranRing (chemistry)MetathesisChemical synthesisAnti-Bacterial Agentschemistry.chemical_compoundLactoneschemistryHemiacetalMacrolidesLactoneThe Journal of organic chemistry
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Regio- and diastereoselective fluorination of alicyclic β-amino acids.

2011

A regio- and stereoselective approach to fluorinated β-aminocyclohexene or cyclohexane esters has been developed, starting from a bicyclic β-lactam (1). The procedure involves six or seven steps, based on regio- and stereoselective iodolactonization, lactone opening and hydroxy–fluorine exchange. The method has been extended to the synthesis of fluorinated amino ester enantiomers.

chemistry.chemical_classificationModels MolecularCyclohexaneBicyclic moleculeStereochemistryOrganic ChemistryIodolactonizationMolecular ConformationStereoisomerismCrystallography X-RayBiochemistryAmino acidchemistry.chemical_compoundAlicyclic compoundchemistryOrganic chemistryStereoselectivityPhysical and Theoretical ChemistryEnantiomerAmino AcidsLactoneOrganicbiomolecular chemistry
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Tandem asymmetric Michael reaction-intramolecular Michael addition. An easy entry to chiral fluorinated 1,4-dihydropyridines.

2010

A novel one-pot tandem asymmetric Hantzsch-type process has been employed to generate fluorinated 1,4-dihydropyridines (1,4-DHPs) as single diastereoisomers. It involves the condensation of (R)-(+)-allyl p-tolyl sulfoxide, fluorinated nitriles, and alkyl propiolates, giving access to a new family of enantiomerically pure fluorine-containing 1,4-DHPs.

chemistry.chemical_classificationModels MolecularDihydropyridinesTandemHydrocarbons FluorinatedMolecular StructureChemistryOrganic ChemistryDiastereomerSulfoxideStereoisomerismBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundIntramolecular forceAlkynesMichael reactionOrganic chemistryCombinatorial Chemistry TechniquesPhysical and Theoretical ChemistryAlkylOrganic letters
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Asymmetric synthesis of fluorinated amino macrolactones through ring-closing metathesis

2007

The synthesis of new chiral fluorinated amino and azamacrolactones of types 1 and 2 is described. A ring-closing metathesis (RCM) reaction constitutes the key step in this methodology, which uses fluorinated amino alcohols 7 as starting materials. The influence of the CF2 group, which is located in the alpha-position relative to the carbon bearing the amino group, on the efficiency of the RCM reaction is noteworthy. This method allows for the preparation of the desired fluorinated macrolactones in excellent yields.

chemistry.chemical_classificationModels MolecularMacrocyclic CompoundsHydrocarbons FluorinatedMolecular StructureOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismMetathesisCrystallography X-RayCombinatorial chemistryChemical synthesisAmino AlcoholsLactonesRing-closing metathesischemistryCyclizationMoleculeAmine gas treatingLactone
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Cooperative supramolecular polymerization and amplification of chirality in C3-symmetrical OPE-based trisamides.

2011

Sergeants-and-soldiers experiments demonstrate the amplification of chirality that transforms the racemic mixture of helical columns formed from OPE-based trisamides into enantiomerically enriched helical structures (see scheme).The cooperative supramolecular polymerization of the trisamides is investigated by theoretical calculations and temperature-dependent UV/Vis and CD experiments. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

chemistry.chemical_classificationModels MolecularMolecular StructureOrganic ChemistrySupramolecular chemistryStereoisomerismGeneral ChemistryAmidesCatalysisPolymerizationSupramolecular polymersCrystallographychemistryPolymerizationRacemic mixtureSelf-assemblyChirality (chemistry)Chemistry (Weinheim an der Bergstrasse, Germany)
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Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

2005

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.

chemistry.chemical_classificationModels MolecularOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructurePHOTOCHEMICAL BEHAVIORChemistryPhotochemistryUltraviolet RaysOrganic ChemistryPATHWAYSSettore CHIM/06 - Chimica OrganicaRing (chemistry)PhotochemistryHeterocyclic compoundCyclizationZeolitesZeolite
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Asymmetric One-Pot Synthesis of (3R,3aS,6aR)-Hexahydrofuro[2,3-b]furan-3-ol: A Key Component of Current HIV Protease Inhibitors

2017

A concise and efficient synthesis of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-ol, a key building block for several clinical and experimental HIV protease inhibitors including the highly important drug darunavir, was achieved via a one-pot procedure using furan and Cbz-protected glycol aldehyde as starting materials. A [2+2]-photocycloaddition between both reactants which can be prepared from wood-based starting materials according to the principles of xylochemistry, followed by hydrogenation and lipase-catalyzed kinetic resolution afforded the target compound in high yield and up to 99% ee.

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryOrganic ChemistryOne-pot synthesisChemistry OrganicStereoisomerismStereoisomerismHIV Protease Inhibitors010402 general chemistry01 natural sciencesAldehyde0104 chemical sciencesKinetic resolutionchemistry.chemical_compoundFuranYield (chemistry)medicineOrganic chemistryHIV Protease InhibitorFuransDarunavirmedicine.drugThe Journal of Organic Chemistry
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Molecular aggregation in selected crystalline 1:1 complexes of hydrophobicD- andL-amino acids. IV. TheL-phenylalanine series

2009

The amino acid L-phenylalanine has been cocrystallized with D-2-aminobutyric acid, C(9)H(11)NO(2).C(4)H(9)NO(2), D-norvaline, C(9)H(11)NO(2).C(5)H(11)NO(2), and D-methionine, C(9)H(11)NO(2).C(5)H(11)NO(2)S, with linear side chains, as well as with D-leucine, C(9)H(11)NO(2).C(6)H(13)NO(2), D-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), and D-allo-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), with branched side chains. The structures of these 1:1 complexes fall into two classes based on the observed hydrogen-bonding pattern. From a comparison with other L:D complexes involving hydrophobic amino acids and regular racemates, it is shown that the structure-directing properties of phenylalanine closel…

chemistry.chemical_classificationMolecular StructureChemistryStereochemistryAminobutyratesPhenylalanineHydrogen BondingStereoisomerismStereoisomerismPhenylalanineGeneral MedicineCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyAmino acidValineSide chainIsoleucineLeucineAminobutyratesHydrophobic and Hydrophilic InteractionsActa Crystallographica Section C Crystal Structure Communications
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N-Methyldehydroamino acids promote a configuration cis of N-methylamide bond

2008

Abstract Dehydroamino acids with a methylated N-terminal tertiary amide bond occur in natural small cyclic peptide toxins. To investigate their conformational preferences a systematic theoretical analysis was performed on N ′-methylamides of N -acetyl- N -methyldehydroamino acids (Ac-Δ(Me)Xaa-NHMe, where Xaa = ( Z )-Abu, ( E )-Abu, Val, ( Z )-Phe, and ( E )-Phe) considering the configuration trans and cis of the tertiary amide bond. The ϕ , ψ potential energy surfaces were calculated at the B3LYP/6-31+G ∗∗ //HF/3-21G level with inclusion of the solvent (water) effect (SCRF method). The conformers localised were fully optimised at the B3LYP/6-31+G ∗∗ in vacuo. The accessible areas of the pot…

chemistry.chemical_classificationN-MethylationNodularinDehydroamino acidsDouble bondStereochemistryHydrogen bondMicrocystinMethylamidePotential energy surfaceCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundchemistryAmidePeptide bondTentoxinPhysical and Theoretical Chemistrytrans–cis isomerisationConformational isomerismIsomerizationCis–trans isomerismJournal of Molecular Structure: THEOCHEM
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