Search results for "Nucleophile"

showing 5 items of 385 documents

A Catalyst Designed for the Enantioselective Construction of Methyl- and Alkyl-Substituted Tertiary Stereocenters

2015

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…

natural productsSubstituentKetene010402 general chemistry01 natural sciencesCatalysisStereocenterchemistry.chemical_compoundNucleophileOrganic chemistryorganocatalysista116Alkylchemistry.chemical_classification010405 organic chemistryChemistryEnantioselective synthesisIminiumasymmetric catalysisGeneral MedicineGeneral Chemistrydiastereoselectivity0104 chemical sciences3. Good healthOrganocatalysisdensity functional calculationsAngewandte Chemie International Edition
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Noncovalent axial I∙∙∙Pt∙∙∙I interactions in platinum(II) complexes strengthen in the excited state

2021

Abstract Coordination compounds of platinum(II) participate in various noncovalent axial interactions involving metal center. Weakly bound axial ligands can be electrophilic or nucleophilic; however, interactions with nucleophiles are compromised by electron density clashing. Consequently, simultaneous axial interaction of platinum(II) with two nucleophilic ligands is almost unprecedented. Herein, we report structural and computational study of a platinum(II) complex possessing such intramolecular noncovalent I⋅⋅⋅Pt⋅⋅⋅I interactions. Structural analysis indicates that the two iodine atoms approach the platinum(II) center in a “side‐on” fashion and act as nucleophilic ligands. According to c…

platinakemialliset yhdisteetchemistry.chemical_elementfysikaalinen kemiaCoordination complexMetaljodinoncovalent interactionsNucleophileaxial interactionsexcited stateNon-covalent interactionsplatinumPhysical and Theoretical Chemistryexcited stateschemistry.chemical_classificationiodineCommunicationliganditAtomic and Molecular Physics and OpticsCommunicationsCrystallographychemistryCovalent bondvisual_artExcited stateIntramolecular forcevisual_art.visual_art_mediumPlatinum
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Diversity of Isomerization Patterns and Protolytic Forms in Aminocarbene PdII and PtII Complexes Formed upon Addition of N,N′-Diphenylguanidine to Me…

2017

Reaction of the palladium(II) and platinum(II) isocyanide complexes cis-[MCl2(CNR)2] [M = Pd, R = C6H3(2,6-Me2) (Xyl), 2-Cl-6-MeC6H3, cyclohexyl (Cy), t-Bu, C(Me)2CH2(Me)3 (1,1,3,3-tetramethylbuth-1-yl abbreviated as tmbu); M = Pt, R = Xyl, 2-Cl-6-MeC6H3, Cy, t-Bu, and tmbu] with N,N′-diphenylguanidine (DPG) leads to DPG-derived metal-bound deprotonated acyclic diaminocarbene (ADC) species. This reaction occurs via a two-step process, involving the initial coupling of the guanidine with one of the isocyanides and leading to deprotonated monocarbene monochelated species, while the next addition grants the deprotonated bis-carbene bis-chelated metal compounds. DPG behaves as nucleophile, depr…

protolytic forms010405 organic chemistryStereochemistryIsocyanideOrganic ChemistrySubstituentchemistry.chemical_elementRegioselectivityaminocarbene complexes010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesdiversityInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryNucleophileisomerization patternsPhysical and Theoretical ChemistryGuanidineIsomerizationta116PalladiumOrganometallics
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Low‐Valent Germanylidene Anions: Efficient Single‐Site Nucleophiles for Activation of Small Molecules

2021

Abstract Rare mononuclear and helical chain low‐valent germanylidene anions supported by cyclic (alkyl)(amino)carbene and hypermetallyl ligands were synthesised by stepwise reduction from corresponding germylene precursors via stable and isolable germanium radicals. The electronic structures of the anions can be described with ylidene and ylidone resonance forms with the Ge−C π‐electrons capable of binding even weak electrophiles. The germanylidene anions reacted with CO2 to give μ‐CO2‐κC:κO complexes, a rare coordination mode for low‐valent germanium and inaccessible for the related neutral germylones. These results implicate low‐valent germanylidene anions as efficient single‐site nucleop…

small molecule activationkemialliset yhdisteetdonor-acceptor systemsRadical010402 general chemistry01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundsub-valent compoundsNucleophilemain group elementsAlkylchemistry.chemical_classificationkemialliset reaktiot010405 organic chemistryChemistryCommunicationOrganic ChemistrymolekyylitGeneral ChemistryResonance (chemistry)Small moleculeCommunications0104 chemical sciences3. Good healthgermaniumaktivointiMain group elementElectrophileCarbenevalenssi (kemia)Chemistry – A European Journal
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Fluorinated heterocyclic compounds: an assay on the photochemistry of some fluorinated 1-oxa-2-azoles: an expedient route to fluorinated heterocycles

2004

Abstract Photoinduced heterocyclic rearrangements of ON bond-containing azoles have been claimed in the synthesis of target fluorinated heterocyclic compounds. In this context, the photochemical behavior of some fluorinated 1,2,4-oxadiazoles has been investigated. Irradiations of 3-amino-5-perfluoroalkyl-1,2,4-oxadiazoles at λ =313 nm in methanol gave open-chain products arising from a reaction of the nucleophilic solvent with either the first formed ring-photolytic species or with a nitrilimine moiety generated from it. Differently, irradiations in methanol with the presence of triethylamine (TEA) followed competing phototransposition pathways leading to the ring-isomers 2-amino-5-perfluo…

synthesisFluorinated heterocyclic compounds Oxadiazoles Synthesis Photochemistry Molecular rearrangementsfluorinated heterocyclic compounds;oxadiazoles;synthesis;photochemistry;molecular rearrangementsmolecular rearrangementsContext (language use)PhotochemistryBiochemistryInorganic Chemistrychemistry.chemical_compoundNucleophileEnvironmental ChemistryMoietySettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryTriethylaminephotochemistryNitrilimineOrganic ChemistryoxadiazolesSettore CHIM/06 - Chimica OrganicaGeneral MedicineSolventchemistryfluorinated heterocyclic compoundsMethanolSolvolysis
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