Search results for "boranes"

showing 5 items of 45 documents

Receptor-mediated uptake of boron-rich neuropeptide y analogues for boron neutron capture therapy.

2014

Peptidic ligands selectively targeting distinct G protein-coupled receptors that are highly expressed in tumor tissue represent a promising approach in drug delivery. Receptor-preferring analogues of neuropeptide Y (NPY) bind and activate the human Y1 receptor subtype (hY1 receptor), which is found in 90% of breast cancer tissue and in all breast-cancer-derived metastases. Herein, novel highly boron-loaded Y1 -receptor-preferring peptide analogues are described as smart shuttle systems for carbaboranes as (10) B-containing moieties. Various positions in the peptide were screened for their susceptibility to carbaborane modification, and the most promising positions were chosen to create a mu…

inorganic chemicalsStereochemistrymedia_common.quotation_subjectMolecular Sequence Datachemistry.chemical_elementPeptideBoron Neutron Capture TherapyBreast NeoplasmsBiochemistrySolid-phase synthesisDrug DiscoveryChlorocebus aethiopsAnimalsHumansNeuropeptide YAmino Acid SequenceGeneral Pharmacology Toxicology and PharmaceuticsReceptorInternalizationBoronBoranesmedia_commonPharmacologychemistry.chemical_classificationChemistryOrganic ChemistryReceptor-mediated endocytosisNeuropeptide Y receptorReceptors Neuropeptide YHEK293 CellsDrug deliveryCOS CellsMolecular MedicineFemaleChemMedChem
researchProduct

Icosahedral carboranes as scaffolds for congested regioselective polyaryl compounds : the distinct distance tuning of C-C and its antipodal B-B

2019

Four-fold aryl substituted o-carborane derivatives with defined patterns of substitution at the antipodal region of the cluster carbon atoms have been achieved. It is proven that this region is congested but lacks steric hindrance. Also, the two antipodal sites Cc-Cc and B9-B12 are affected very distinctly by electron donor substituents. peerReviewed

klusteritcarboraneskemialliset yhdisteetbooricluster compounds
researchProduct

P-C Cross-Coupling Onto Enamides: Versatile Synthesis of α-Enamido Phosphane Derivatives

2012

We report herein the Pd-catalyzed P–C cross-coupling reac- tion between enol phosphates and secondary phosphane–bor- ane complexes or phosphane oxides. The reaction was per- formed under mild conditions, owing to Pd activation of the P–H bonds of the phosphane–boranes (or phosphane oxides) and to the powerful enol phosphate coupling reagents. New useful chiral and achiral α - β -alkenylphosphane derivatives bearing an amido group in the α -position to the P center were obtained in yields up to 70 %.

phosphaalkenesStereochemistryboranesOrganic ChemistryphosphanesBoranesPhosphateEnolMedicinal chemistryCoupling (electronics)chemistry.chemical_compoundchemistryenolsReagentcross-couplingPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
researchProduct

Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
researchProduct

Synthesis, Characterization, and Properties of Weakly Coordinating Anions Based on tris-Perfluoro-tert-Butoxyborane

2017

Abstract Image A convenient method for the preparation of strongly Lewis acidic tris-perfluoro-tert-butoxyborane B(ORF)3 (1), (ORF = OC(CF3)3) was developed, and its X-ray structure was determined. 1 was used as a precursor, guided by density functional theory (DFT) calculations and volume-based thermodynamics, for the synthesis of [NEt4][NCB(ORF)3] (3) and [NMe4][FB(ORF)3] (5) and the novel large and weakly coordinating anion salts [Li 15-Crown-5][B(ORF)4] (2) and [NEt4][CN{B(ORF)3}2] (4). The stability of [B(ORF)4]− was compared with that of some related known weakly coordinating anions by appropriate DFT calculations. peerReviewed

weakly coordinating anionsboranesLewis acidssynteesi
researchProduct