Search results for "BOND"

showing 10 items of 3527 documents

Designing conjugated microporous polymers for visible light-promoted photocatalytic carbon–carbon double bond cleavage in aqueous medium

2018

The production of valuable carbonyl compounds directly from alkenes via carbon–carbon double (CC) bond cleavage is a highly important reaction. As a promising alternative to traditional metal-catalyzed thermal reaction conditions, photocatalysis offers an environmentally friendly and sustainable synthetic strategy. However, most photocatalysts used so far were homogeneous, molecular and transition metal-based catalytic systems. Here, we report a structural design strategy of conjugated microporous polymers (CMPs) as a class of metal-free, heterogeneous, stable and reusable photocatalysts for visible light-promoted CC bond cleavage reaction. Via different electron donor and acceptor combinat…

chemistry.chemical_classificationDouble bondRenewable Energy Sustainability and the EnvironmentElectron donor02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesCatalysisConjugated microporous polymerchemistry.chemical_compoundchemistryBenzothiazoleTransition metalPhotocatalysisGeneral Materials Science0210 nano-technologyBond cleavageJournal of Materials Chemistry A
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1,2-Dipolar addition model for the cytoprotective activity of selected α,β-unsaturated compounds with CO functionality: an ab initio study

2001

Abstract The mechanism of the addition of a nucleophile (an alkylthiol group) to a double bond of α,β-unsaturated systems in the gas phase was explored. In this study, intermediates of the reaction were also investigated using ab initio calculations (RHF/6-31G ∗ and MP2/6-31+G ∗ ). Our results indicate that direct dipolar attack of the S–H group of an alkylthiol on the CC double bond is a reasonable reaction path. The present results represent, therefore, additional support for our hypothesis. This suggests that the mechanism of cytoprotection might be mediated, at least in part, by a reaction between the olefinic acceptor and the sulfhydryl-containing groups of the mucosa.

chemistry.chemical_classificationDouble bondStereochemistryAb initioCondensed Matter PhysicsBiochemistryAcceptorCytoprotectionDipolechemistryNucleophileComputational chemistryAb initio quantum chemistry methodsReaction pathPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Synthesis of peptides with α,β‐dehydroamino acids, V. coupling experiments with C‐terminal dehydrophenylalanine and dehydroalanine residues

1986

N-Protected model dipeptides of C-terminal (Z)-ΔPhe and ΔAla couple with glycine esters after activation with either diphenyl phosphorazidate (DPPA), N-cyclohexyl-N′-[2-(N-methylmorpholinio)ethyl]carbodiimide p-toluenesulfonate (WSC), N,N′-dicyclohexylcarbodiimide + 1-hydroxybenzotriazole (DCC + HOBt), or the mixed anhydride (MA) with isobutyl chlorocarbonate to give in good or mostly moderate yields the (Z)-ΔPhe-containing tripeptides 1 – 9 and ΔAla-containing tripeptides 11 – 19, respectively. In the MA and DPPA methods, further acylation products 20a – d are formed to a great extent, expecially during the ΔAla peptide syntheses. (E)-TFA-Gly-ΔPhe and Gly-OtBu, irrespective of the activati…

chemistry.chemical_classificationDouble bondStereochemistryChemistryOrganic ChemistryPeptideTripeptideAdductAcylationchemistry.chemical_compoundDehydroalaninePhysical and Theoretical ChemistryActivation methodCarbodiimideLiebigs Annalen der Chemie
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Synthesis of novel functionalized cispentacins through C–C oxidative cleavage of diendo-norbornene β-amino acid

2013

Difunctionalized cispentacin derivatives with two new stereogenic centres have been synthesized from a diendo-norbornene β-amino acid in a stereocontrolled route, involving C–C double bond functionalization by dihydroxylation, followed by oxidative ring cleavage and transformation of the dialdehyde intermediates through a Wittig reaction.

chemistry.chemical_classificationDouble bondStereochemistryGeneral Chemical EngineeringGeneral ChemistryOxidative phosphorylationCleavage (embryo)Amino acidStereocenterchemistry.chemical_compoundchemistryDihydroxylationWittig reactionta116NorborneneRSC Advances
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Synthetic Approaches to Anti-Inflammatory Macrolactones of the Oxacyclododecindione Type

2015

Various synthetic approaches to the oxacyclododecindione-type macrolactones, known for their potent anti-inflammatory activity, are presented. These include an attempted carbonylative ring closure, a hydroacylation route, and an approach by ring-closing metathesis and double bond isomerization, as well as a strategy including ring-closing metathesis/unsaturation. The last route allowed the preparation of a bioactive analogue of the recently described 14-deoxyoxacyclododecindione.

chemistry.chemical_classificationDouble bondStereochemistrymedicine.drug_classOrganic ChemistryHydroacylationTotal synthesisMetathesisRing (chemistry)Anti-inflammatoryRing-closing metathesischemistrymedicinePhysical and Theoretical ChemistryIsomerizationEuropean Journal of Organic Chemistry
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Naphthothiete und ihre Anwendung in der Heterocyclen-Synthese

1995

Naphtothietes and Their Application to the Synthesis of Heterocycles The three isomeric naphthothietes 5, 11, and 16 were prepared according to the reaction sequences shown in Schemes 1–3. The final step was in each case a flash vacuum pyrolysis (FVP) of the corresponding mercaptonaphthalenemethanol 4, 9, and 15, respectively. The thiete rings in 5 and 11 can be opened by gentle heating; the ring opening of the isomer 16 possesses a much higher activation barrier. A MNDO calculation of the ΔHf values of 5, 11, and 16 and the open isomers 5′, 11′, and 16′ provides an explanation for the different behavior. Photochemical ring opening represents a useful alternative. The reaction Schemes 4, 6,…

chemistry.chemical_classificationDouble bondchemistryActivation barrierFlash vacuum pyrolysisStereochemistryOrganic ChemistryMNDOGeneral ChemistryPhysical and Theoretical ChemistryRing (chemistry)Medicinal chemistryCycloadditionLiebigs Annalen
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The transformation of aromatic molecules into the subspace of their double bonds

1975

A model of new submolecules is presented. As an application some absorptions of aromatic radicals are interpreted in UV and visible spectra. Extension of the model to biological systems is prejudged.

chemistry.chemical_classificationDouble bondchemistryComputational chemistryRadicalMoleculeChiropracticsPhysical and Theoretical ChemistrySubspace topologyTransformation (music)Spectral lineTheoretica Chimica Acta
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ChemInform Abstract: Cycloaddition Reactions of Benzothiete and Hetero Dienophiles for the Synthesis of Heterocyclic Systems.

1987

Abstract Benzothiete ( 1 ) undergoes cycloaddition reactions with hetero dienophiles with NN-, NO- or CO- double bonds, leading to six-membered heterocyclic ring systems of 2H-3,4-dihydro-1,2,3-benzothiadiazine ( 3 ), 4H-3,1,2-benzoxathiazine ( 4 ) and 4H-3,1-benzoxathiin.

chemistry.chemical_classificationDouble bondchemistryGeneral MedicineRing (chemistry)Medicinal chemistryCycloadditionChemInform
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ChemInform Abstract: Synthetic Approaches to Antiinflammatory Macrolactones of the Oxacyclododecindione Type.

2015

A variety of attempts to synthesize oxacyclododecindione macrolactones through carbonylative ring-closure, intramolecular alkyne hydroacyalation, and Ru-catalyzed double bond isomerization fails.

chemistry.chemical_classificationDouble bondchemistryStereochemistryIntramolecular forceSalt metathesis reactionOxacyclododecindioneAlkyneGeneral MedicineIsomerizationChemInform
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Cycloaddition Reactions of 2H-Benzo[b]thiete and Thiocarbonyl Compounds

1997

2H-Benzo[b]thiete (1) reacts in the o-quinoid form 1′ with the cyclic trithiocarbonates 4 and 6a, b and with the thioketones 8, 10 and 12 in [8π + 2π] cycloaddition reactions to the spiro compounds 5, 7a, b, 9, 11a, b. Irrespective of the presence of CC double bonds, chemoselective and regioselective addition processes at the CS double bonds take place that lead to 4H-1,3-benzodithianes.

chemistry.chemical_classificationDouble bondchemistryStereochemistryOrganic ChemistryRegioselectivityGeneral ChemistryPhysical and Theoretical ChemistryMedicinal chemistryCycloadditionLiebigs Annalen
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