Search results for "enolate"

showing 10 items of 52 documents

CCDC 232959: Experimental Crystal Structure Determination

2005

Related Article: F.Thetiot, S.Triki, J.S.Pala, J.-R.Galan-Mascaros, J.M.Martinez-Agudo, K.R.Dunbar|2004|Eur.J.Inorg.Chem.||3783|doi:10.1002/ejic.200400203

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates(mu~2~-22'-bipyrimidine)-tetrakis(22-dicyanoethoxyethenolate)-tetraaqua-di-copper(ii) dihydrate
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CCDC 2060890: Experimental Crystal Structure Determination

2021

Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates2-amino-4-(3456-tetrahydropyrimidin-1-ium-2-yl)phenolate monohydrate
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CCDC 855780: Experimental Crystal Structure Determination

2012

Related Article: K.Salorinne, E.Nauha, M.Nissinen|2012|Chem.Asian J.|7|809|doi:10.1002/asia.201100969

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu~3~-281420-Tetraethyl-6121824-tetramethoxy-410:1622-bis(369-trithiaundecane-111-dioxy)calix(4)arene)-bis(246-trinitrophenolato)-bis(acetonitrile)-tetra-silver bis(246-trinitrophenolate) acetonitrile solvateExperimental 3D Coordinates
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CCDC 232956: Experimental Crystal Structure Determination

2005

Related Article: F.Thetiot, S.Triki, J.S.Pala, J.-R.Galan-Mascaros, J.M.Martinez-Agudo, K.R.Dunbar|2004|Eur.J.Inorg.Chem.||3783|doi:10.1002/ejic.200400203

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-((mu~2~-22'-bipyrimidine)-bis(mu~2~-22-dicyanoethoxyethenolate)-diaqua-bis(22-dicyanoethoxyethenolate)-di-manganese(ii))Experimental 3D Coordinates
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CCDC 2060885: Experimental Crystal Structure Determination

2021

Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametershydrogen bis(2-amino-4-[amino(iminio)methyl]phenolate) chloride dihydrateExperimental 3D Coordinates
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CCDC 2060886: Experimental Crystal Structure Determination

2021

Related Article: Lucija Ptiček, Lucija Hok, Petra Grbčić, Filip Topić, Mario Cetina, Kari Rissanen, Sandra Kraljević Pavelić, Robert Vianello, Livio Racané|2021|Org.Biomol.Chem.|19|2784|doi:10.1039/D1OB00235J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametershydrogen bis(2-amino-4-[amino(iminio)methyl]phenolate) chloride dihydrateExperimental 3D Coordinates
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CCDC 232957: Experimental Crystal Structure Determination

2005

Related Article: F.Thetiot, S.Triki, J.S.Pala, J.-R.Galan-Mascaros, J.M.Martinez-Agudo, K.R.Dunbar|2004|Eur.J.Inorg.Chem.||3783|doi:10.1002/ejic.200400203

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-((mu~2~-22'-bipyrimidine)-bis(mu~2~-22-dicyanoethoxyethenolate)-diaqua-bis(22-dicyanoethoxyethenolate)-di-cobalt(ii))Cell ParametersExperimental 3D Coordinates
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Conformationally Locked Pyramidality Explains the Diastereoselectivity in the Methylation of trans-Fused Butyrolactones

2020

A stereoselectivity model inspired by the total synthesis of stemona alkaloids is developed to explain why enolate-derived 3,4-fused butyrolactones are methylated with a preference for syn alkylation. The model shows how conformational locking present in nonplanar enolate structures favors syn over anti methylation, due to less significant structural distortions in the syn pathway. The developed model was also successfully used to rationalize selectivities of previously documented methylation reactions. peerReviewed

StemonaLetterisomeriaStereochemistrytransition states010402 general chemistry01 natural sciencesBiochemistryenolatesheterocyclic compoundsPhysical and Theoretical Chemistryorgaaniset yhdisteetkemialliset reaktiotbiology010405 organic chemistryChemistryorganic chemicalsOrganic ChemistryselectivityTotal synthesisMethylationbiology.organism_classification0104 chemical sciencesalkaloiditchemical structureorganic reactionsStereoselectivityOrganic Letters
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Steric vs. electronic stereocontrol in syndio- or iso-selective ROP of functional chiral β-lactones mediated by achiral yttrium-bisphenolate complexes

2018

International audience; Origins of stereoselectivity in ROP of racemic chiral cyclic esters promoted by achiral yttrium complexes, resulting in the formation of highly heterotactic polylactide, and highly syndiotactic or, more uniquely, highly isotactic poly(3-hydroxybutyrate)s, are discussed. A close interplay between the nature of the cyclic ester, most particularly of the exocyclic functional chain installed on the chiral center of β-lactones, and the ortho-substituents installed on the phenolate rings of the ligand, results in various determining secondary interactions of steric and also electronic nature.

Steric effectsStereochemistryisomeriachemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisTacticityMaterials Chemistry[CHIM]Chemical Sciencesta116steric vs. electronic stereocontrol010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryMetals and AlloysGeneral ChemistryYttriumkompleksiyhdisteetachiral yttrium-bisphenolate complexes0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistryfunctional chiral β-lactonesCeramics and CompositesStereoselectivity
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Azathioprine, Mycophenolate Mofetil, and Methotrexate Specifically Modulate Cytokine Production by T Cells

1998

T-Lymphocytesmedicine.medical_treatmentAzathioprinePharmacologyMycophenolateGeneral Biochemistry Genetics and Molecular BiologyInterferon-gammaMiceHistory and Philosophy of ScienceAzathioprinemedicineAnimalsCells CulturedMice Inbred BALB CTumor Necrosis Factor-alphabusiness.industryGeneral NeuroscienceMycophenolic AcidMethotrexateCytokineCytokinesMethotrexatebusinessImmunosuppressive AgentsSpleenmedicine.drugAnnals of the New York Academy of Sciences
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