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Journal of materials chemistry. C, Materials for optical and electronic devices, ISSN 2050-7526, 2014, Volume 2, Issue 38, pp. 8089 - 8097
We report on the synthesis and properties of 6,6′-dithienylindigo (DTI) and poly(DTI). Redox chemistry and ambipolar charge transport with = 0.11 cm V s and =... 
CROSS-COUPLING REACTIONS | PHYSICS, APPLIED | FILMS | COLOR | MATERIALS SCIENCE, MULTIDISCIPLINARY | PIGMENTS | INDIGO | Electrodes | Reduction | Stability | Field effect transistors | Vanadium | Electronics | Derivatives | Devices
Journal Article
Chemistry : a European journal, ISSN 1521-3765, 2018, Volume 24, Issue 68, pp. 17975 - 17985
At the catalytic site for the hydrolysis of cellulose the enzyme cellobiohydrolase Cel7A binds the enantiomers of the adrenergic beta‐blocker propranolol with... 
enzymes | nuclear Overhauser effect | NMR spectroscopy | ligand–protein interactions | propranolol | MOLECULAR-DYNAMICS | LIGAND-BINDING | ligand-protein interactions | ACTIVE-SITE | TRICHODERMA-REESEI | CRYSTAL-STRUCTURE | STATIONARY PHASES | CHEMISTRY, MULTIDISCIPLINARY | PROTON COUPLING-CONSTANTS | TRANSFER DIFFERENCE NMR | STD-NMR | COMPLETE RELAXATION | Catalytic Domain | Hypocrea - enzymology | Crystallography, X-Ray | Hypocrea - chemistry | Isomerism | Molecular Dynamics Simulation | Cellulose 1,4-beta-Cellobiosidase - chemistry | Thermodynamics | Hypocrea - metabolism | Cellulose 1,4-beta-Cellobiosidase - metabolism | Propranolol - metabolism | Nuclear Magnetic Resonance, Biomolecular | Molecular Docking Simulation | Propranolol - analogs & derivatives | Binding Sites | Propranolol hydrochloride | Nuclear magnetic resonance spectroscopy | Spin coupling | Enantiomers | Protein binding | Binding | Oxygen | Enthalpy | Cellulose | Cellobiohydrolase | Overhauser effect | Molecular dynamics | Entropy | Selectivity | Isomers | Substrates | Coupling (molecular) | Magnetic resonance spectroscopy | Proteins | Affinity | Ligands | Catalysis | Propranolol | Protein interaction | Coordination compounds | Hydroxyl groups | Crystal structure | Naturvetenskap | Kemi | Organisk kemi | Natural Sciences | Chemical Sciences | Organic Chemistry
Journal Article
ORGANIC & BIOMOLECULAR CHEMISTRY, ISSN 1477-0520, 12/2016, Volume 15, Issue 1, pp. 17 - 33
.../c6ob02099b www.rsc.org/obc An overview of the synthesis of acyl hydrazides from aldehydes and reactions of the products thereof André Shamsabadi and Vijay Chudasama... 
ORGANIC-SYNTHESIS | EFFICIENT HYDROACYLATION REACTION | CATALYZED HYDROACYLATION | CONVERSION | STRATEGY | BOND FUNCTIONALIZATION | AZODICARBOXYLATES | CHEMISTRY, ORGANIC | ACETATE | C-H ACTIVATION | DERIVATIVES
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 2017, Volume 15, Issue 1, pp. 17 - 33
Herein a review on the methods for the formation and reaction of acyl hydrazides will be given. There is particular focus on the synthesis of acyl hydrazides... 
Journal Article
Journal of materials chemistry. C, Materials for optical and electronic devices, ISSN 2050-7534, 2015, Volume 3, Issue 35, pp. 9170 - 9174
The synthesis, optoelectronic properties and near-infrared electroluminescent heterojunctions of a twisted and soluble 7,8,15,16,23,24-hexaazatrianthrylene... 
LIGHT-EMITTING-DIODES | BASES | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | PHENAZINE DERIVATIVES | POLYMER | PYRENE-FUSED AZAACENES | EMISSION | Heterojunctions | Optoelectronics | Electroluminescence | Synthesis | Electronic devices | Derivatives
Journal Article
Current Organic Chemistry, ISSN 1385-2728, 10/2014, Volume 18, Issue 20, pp. 2646 - 2651
Continuing our research programme to develop the synthesis of small heterocyclic entities, in the present study we prepared carbohydrazides of privileged... 
MABA | Carbo-hydrazides | Mtb | Coumarin | ANTIMYCOBACTERIAL ACTIVITY | carbo-hydrazides | 3D-QSAR | CHEMISTRY, ORGANIC | HRv | DRUG-RESISTANT TUBERCULOSIS | CHALLENGES | COUMARINS | QSAR | 1,4-DIHYDROPYRIDINES | AGENTS | ANTITUBERCULAR ACTIVITY | DERIVATIVES
Journal Article
Journal of the Mexican Chemical Society, ISSN 1870-249X, 2017, Volume 61, Issue 1, pp. 23 - 27
Here we report a simple and efficient protocol for selectively diamine protection with Boc using Me3SiCl or SOCl2 as HCl source in "one-pot" procedure. This... 
Diamines | Cyclohexane-1 | 2-diamine | 2-diphenylethane1 | Chiral | Boc monoprotection | ASYMMETRIC TRANSFER HYDROGENATION | COMPLEXES | cyclohexane-1,2-diamine | CHEMISTRY, MULTIDISCIPLINARY | KETONES | ORGANOCATALYSTS | LIGANDS | ATH | RUTHENIUM(II) | 1,2-diphenylethane-1,2-diamine | TRANS-1,2-DIAMINOCYCLOHEXANE | DERIVATIVES | diamines | WATER | Chemistry, Multidisciplinary
Journal Article
Journal of organometallic chemistry, ISSN 0022-328X, 2019, Volume 904, p. 121007
Novel nido-carboranyl azide [7-N3CH2CH2OCH2CH2O-7,8-C2B9H11]- was prepared by the reaction of 1-hydroxy-ortho-carborane with bis(2-chloroethyl) ether followed... 
Carboranes | Azides | Cycloaddition | Click chemistry | bis(2-chloroethyl) ether | DRUG | CHEMISTRY, ORGANIC | FUNCTIONAL-DERIVATIVES | CHEMISTRY, INORGANIC & NUCLEAR | MEDICINAL CHEMISTRY | STAUDINGER LIGATION | BIOCONJUGATION | CLOSO-DODECABORATE ANION | NEUTRON-CAPTURE THERAPY | FACILE | SELECTIVITY
Journal Article
Journal of organic chemistry, ISSN 0022-3263, 03/2019, Volume 84, Issue 6, pp. 3132 - 3147
The cytospolides are a novel group of fungal secondary metabolites first described in 2011. Although all 17 natural derivatives share the same C-14 polyketide... 
OXIDATION | Z-ISOMER | LACTONES | ACIDS | CHEMISTRY, ORGANIC | POWERFUL | STEREOSELECTIVE TOTAL-SYNTHESIS | AZIDE | DERIVATIVES | SELECTIVITY | MIXED ANHYDRIDE
Journal Article