Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 38, pp. 6882 - 6885
A synthesis of the unique bisindole framework present in the mushroom-derived alkaloid sciodole has been achieved, validating a biosynthesis proposal that the...
OXIDATION | FRUIT BODIES | LEAD-TETRAACETATE | PROTECTING GROUP | PYRROLE | RING | CHEMISTRY, ORGANIC | OROIDIN | INDOLE-DERIVATIVES | FLAVOVIRENS
OXIDATION | FRUIT BODIES | LEAD-TETRAACETATE | PROTECTING GROUP | PYRROLE | RING | CHEMISTRY, ORGANIC | OROIDIN | INDOLE-DERIVATIVES | FLAVOVIRENS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 08/2016, Volume 57, Issue 31, pp. 3488 - 3490
The two-step synthesis of 3,4-diacyl-2 -pyran-2-ones was achieved in good yields from dehydroacetic acid via transformation of the hydroxyl group into an acyl...
Dehydroacetic acid | Transformation | C[sbnd]C bond formation | Diacyl-pyranones | Lead tetraacetate | Iodobenzene diacetate | Resveratrol
Dehydroacetic acid | Transformation | C[sbnd]C bond formation | Diacyl-pyranones | Lead tetraacetate | Iodobenzene diacetate | Resveratrol
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2018, Volume 140, Issue 42, pp. 13580 - 13585
We describe a synergistic utilization of cerium photocatalysis and photoinduced electron transfer catalysis that enables an atom- and step-economical ring...
ELECTROGENERATED CHEMILUMINESCENCE | CLEAVAGE REACTIONS | LEAD-TETRAACETATE | VISIBLE-LIGHT PHOTOCATALYSIS | SATURATED ALIPHATIC-ALCOHOLS | C-C BOND | REDUCTION POTENTIALS | CHEMISTRY, MULTIDISCIPLINARY | ELECTRON-TRANSFER PROCESSES | METAL CHARGE-TRANSFER | PHOTOREDOX CATALYSIS
ELECTROGENERATED CHEMILUMINESCENCE | CLEAVAGE REACTIONS | LEAD-TETRAACETATE | VISIBLE-LIGHT PHOTOCATALYSIS | SATURATED ALIPHATIC-ALCOHOLS | C-C BOND | REDUCTION POTENTIALS | CHEMISTRY, MULTIDISCIPLINARY | ELECTRON-TRANSFER PROCESSES | METAL CHARGE-TRANSFER | PHOTOREDOX CATALYSIS
Journal Article
Natural Products Journal, ISSN 2210-3155, 2018, Volume 8, Issue 3, pp. 201 - 206
Journal Article
Chemistry Letters, ISSN 0366-7022, 11/2013, Volume 42, Issue 11, pp. 1388 - 1390
An efficient procedure for the preparation of α-acetoxy ketone derivatives by palladium-catalyzed oxidation reactions employing molecular oxygen as the sole...
ACYLOXY | SELECTIVE OXIDATION | LEAD-TETRAACETATE | ORGANIC-CHEMICALS | CHEMISTRY, MULTIDISCIPLINARY
ACYLOXY | SELECTIVE OXIDATION | LEAD-TETRAACETATE | ORGANIC-CHEMICALS | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 10/2019, Volume 60, Issue 41, p. 151083
α Sulfonamidation of β-ketoesters with sulfonyl azide has been developed for the first time using a catalytic amount of Ru(II) complex to produce the...
Sulfonyl azides | α-Sulfonamidation | Cyclic β-ketoesters | Transition metal catalysis | LEAD-TETRAACETATE | alpha-Sulfonamidation | RING-EXPANSION | 1,3-DICARBONYL COMPOUNDS | HYDROXYLATION | CHEMISTRY, ORGANIC | TRANSFER HYDROGENATION | Cyclic beta-ketoesters | KETO-ESTERS | DIRECT AMINATION | LIGANDS | DICHLOROMETHANE | DERIVATIVES
Sulfonyl azides | α-Sulfonamidation | Cyclic β-ketoesters | Transition metal catalysis | LEAD-TETRAACETATE | alpha-Sulfonamidation | RING-EXPANSION | 1,3-DICARBONYL COMPOUNDS | HYDROXYLATION | CHEMISTRY, ORGANIC | TRANSFER HYDROGENATION | Cyclic beta-ketoesters | KETO-ESTERS | DIRECT AMINATION | LIGANDS | DICHLOROMETHANE | DERIVATIVES
Journal Article
TETRAHEDRON LETTERS, ISSN 0040-4039, 03/2015, Volume 56, Issue 11, pp. 1432 - 1436
An efficient transition-metal-free synthetic method of 1H-indazoles has been developed. The reaction of arylhydrazones in the presence of montmorillonite K-10...
LEAD-TETRAACETATE | ONE-POT SYNTHESIS | AUTOXIDATION | Aerobic oxidation | Montmorillonite K-10 | INDAZOLES | CHEMISTRY, ORGANIC | 1H-Indazole | ARYNES | ODCB | 1-ARYL-1H-INDAZOLES | 1,3-DIPOLAR CYCLOADDITION | 1,3,5-TRISUBSTITUTED PYRAZOLES | BOND | DERIVATIVES
LEAD-TETRAACETATE | ONE-POT SYNTHESIS | AUTOXIDATION | Aerobic oxidation | Montmorillonite K-10 | INDAZOLES | CHEMISTRY, ORGANIC | 1H-Indazole | ARYNES | ODCB | 1-ARYL-1H-INDAZOLES | 1,3-DIPOLAR CYCLOADDITION | 1,3,5-TRISUBSTITUTED PYRAZOLES | BOND | DERIVATIVES
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2018, Volume 83, Issue 2, pp. 588 - 603
We have developed an efficient protocol for the synthesis of C-glycosylated phenanthridines. Tetrafuranos-4-yl and pentapyranos-5-yl radicals, generated from...
H FUNCTIONALIZATION | LEAD-TETRAACETATE | NUCLEOSIDE ANALOGS | COUPLING REACTIONS | CHEMISTRY, ORGANIC | SELECTIVE CLEAVAGE | CARBOHYDRATE RADICALS | PROTECTING GROUPS | CYCLODEXTRINS | DERIVATIVES | EFFICIENT METHOD | Usage | Transition metals | Furans | Glycosylation | Chemical properties | Chemical synthesis
H FUNCTIONALIZATION | LEAD-TETRAACETATE | NUCLEOSIDE ANALOGS | COUPLING REACTIONS | CHEMISTRY, ORGANIC | SELECTIVE CLEAVAGE | CARBOHYDRATE RADICALS | PROTECTING GROUPS | CYCLODEXTRINS | DERIVATIVES | EFFICIENT METHOD | Usage | Transition metals | Furans | Glycosylation | Chemical properties | Chemical synthesis
Journal Article
Chemical Communications, ISSN 1359-7345, 04/2014, Volume 50, Issue 30, pp. 3976 - 3978
A novel copper-catalyzed formal O-H insertion of alpha-diazo-1,3-dicarbonyl compounds to carboxylic acids has been developed, providing a straightforward...
OXIDATION | ORGANIC-SYNTHESIS | LEAD-TETRAACETATE | MANGANIC ACETATE | ALPHA-ACETOXY KETONES | COMPLEXES | CHEMISTRY | POLYVALENT IODINE | DIAZO-COMPOUNDS | METAL-SALTS | CHEMISTRY, MULTIDISCIPLINARY | Insertion | Activation | Carboxylic acids
OXIDATION | ORGANIC-SYNTHESIS | LEAD-TETRAACETATE | MANGANIC ACETATE | ALPHA-ACETOXY KETONES | COMPLEXES | CHEMISTRY | POLYVALENT IODINE | DIAZO-COMPOUNDS | METAL-SALTS | CHEMISTRY, MULTIDISCIPLINARY | Insertion | Activation | Carboxylic acids
Journal Article
Tetrahedron, ISSN 0040-4020, 08/2007, Volume 63, Issue 34, pp. 8274 - 8281
Simple and high-yield procedures for the direct oxidative conversion of various primary alcohols, and primary, secondary, and tertiary amines to the...
Nitrile | 1,3-Diiodo-5,5-dimethylhydantoin | Tertiary amine | Aq NH | Primary amine | Secondary amine | Iodine | Primary alcohol | AMMONIA | 2-IMIDAZOLINES | aq NH3 | COPPER-CATALYZED OXIDATION | LEAD TETRAACETATE | SECONDARY | CHEMISTRY, ORGANIC | ALDEHYDES | secondary amine | OXYGEN | DEHYDROGENATION | 1,3-diiodo-5,5-dimethylhydantoin | primary amine | iodine | nitrile | primary alcohol | tertiary amine | CHLORIDE
Nitrile | 1,3-Diiodo-5,5-dimethylhydantoin | Tertiary amine | Aq NH | Primary amine | Secondary amine | Iodine | Primary alcohol | AMMONIA | 2-IMIDAZOLINES | aq NH3 | COPPER-CATALYZED OXIDATION | LEAD TETRAACETATE | SECONDARY | CHEMISTRY, ORGANIC | ALDEHYDES | secondary amine | OXYGEN | DEHYDROGENATION | 1,3-diiodo-5,5-dimethylhydantoin | primary amine | iodine | nitrile | primary alcohol | tertiary amine | CHLORIDE
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 06/2017, Volume 15, Issue 25, pp. 5337 - 5344
A facile and efficient synthesis of N-acetoxy-N-arylamides through double acylations of hydroxylamines with aldehydes and diacetoxyiodobenzene is reported. The...
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2017, Volume 15, Issue 25, pp. 5337 - 5344
A facile and efficient synthesis of N-acetoxy-N-arylamides through double acylations of hydroxylamines with aldehydes and diacetoxyiodobenzene is reported. The...
LEAD-TETRAACETATE | CATALYZED OXIDATIVE AMIDATION | ONE-POT SYNTHESIS | HYPERVALENT IODINE REAGENT | CHEMISTRY, ORGANIC | COUPLING REAGENTS | ALIPHATIC-AMINES | AMIDE BOND FORMATION | ARYL CHLORIDES | AMINE HYDROCHLORIDE SALTS | CARBOXYLIC-ACIDS
LEAD-TETRAACETATE | CATALYZED OXIDATIVE AMIDATION | ONE-POT SYNTHESIS | HYPERVALENT IODINE REAGENT | CHEMISTRY, ORGANIC | COUPLING REAGENTS | ALIPHATIC-AMINES | AMIDE BOND FORMATION | ARYL CHLORIDES | AMINE HYDROCHLORIDE SALTS | CARBOXYLIC-ACIDS
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 06/2010, Volume 12, Issue 11, pp. 2460 - 2463
A copper-catalyzed methodology to functionalize remote sp(3) C-H bonds in alkyl hydroperoxides is presented. The atom-transfer chlorination utilizes simple...
ION INDUCED DECOMPOSITION | ALKOXY RADICALS | LANOSTANE DERIVATIVES | CUPRIC ION | ATOM-TRANSFER | LEAD TETRAACETATE | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | TRANSFER RADICAL POLYMERIZATION | TRANSANNULAR REACTIONS | METAL-COMPLEXES
ION INDUCED DECOMPOSITION | ALKOXY RADICALS | LANOSTANE DERIVATIVES | CUPRIC ION | ATOM-TRANSFER | LEAD TETRAACETATE | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | TRANSFER RADICAL POLYMERIZATION | TRANSANNULAR REACTIONS | METAL-COMPLEXES
Journal Article
Polymer Chemistry, ISSN 1759-9954, 2018, Volume 9, Issue 8, pp. 961 - 967
Three types of cellulosic samples, including microcrystalline, never-dried sulfite pulp, and Cellets, were selected to test the oxidative capacity of a new...
Journal Article
Carbohydrate Polymers, ISSN 0144-8617, 03/2013, Volume 93, Issue 1, pp. 207 - 215
► The recent advances on selective oxidation of cellulose are described. ► TEMPO oxidation of cellulose, occurs mainly at primary OH groups. ► Non persistent...
Sodium periodate | Cellulose oxidation | Phthalimide-N-oxyl (PINO) | TEMPO | N-hydroxyphthalimide (NHPI) | PRIMARY ALCOHOL GROUPS | SYSTEM | POLYMER SCIENCE | CARBONYL GROUPS | TEMPO-MEDIATED OXIDATION | PINO RADICAL GENERATION | CHEMISTRY, ORGANIC | FIBERS | PERIODATE OXYCELLULOSE | POLYSACCHARIDES | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | REGENERATED CELLULOSE | CHEMISTRY, APPLIED | Carbon Dioxide - chemistry | Cyclic N-Oxides - chemistry | Oxidation-Reduction | Hydroxyl Radical - chemistry | Nitrogen Dioxide - chemistry | Nitrogen Oxides - chemistry | Oxygen - chemistry | Cellulose, Oxidized - chemistry | Polymerization | Phthalimides - chemistry | Aldehydes - chemistry | Surveys | Cellulose
Sodium periodate | Cellulose oxidation | Phthalimide-N-oxyl (PINO) | TEMPO | N-hydroxyphthalimide (NHPI) | PRIMARY ALCOHOL GROUPS | SYSTEM | POLYMER SCIENCE | CARBONYL GROUPS | TEMPO-MEDIATED OXIDATION | PINO RADICAL GENERATION | CHEMISTRY, ORGANIC | FIBERS | PERIODATE OXYCELLULOSE | POLYSACCHARIDES | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | REGENERATED CELLULOSE | CHEMISTRY, APPLIED | Carbon Dioxide - chemistry | Cyclic N-Oxides - chemistry | Oxidation-Reduction | Hydroxyl Radical - chemistry | Nitrogen Dioxide - chemistry | Nitrogen Oxides - chemistry | Oxygen - chemistry | Cellulose, Oxidized - chemistry | Polymerization | Phthalimides - chemistry | Aldehydes - chemistry | Surveys | Cellulose
Journal Article
Biotechnology Advances, ISSN 0734-9750, 03/2017, Volume 35, Issue 2, pp. 251 - 266
Oxidation of the primary OH groups in cellulose is a pivotal reaction both at lab and industrial scale, leading to the value-added products, i.e. oxidized...
Cellulose oxidation | Biofuel | Depolymerisation | Energy conservation | PRIMARY ALCOHOL GROUPS | CARBON-SUPPORTED RUTHENIUM | TEMPO-MEDIATED OXIDATION | PINO RADICAL GENERATION | SOLID-ACID | SUPERCRITICAL WATER GASIFICATION | NONTHERMAL ATMOSPHERIC PLASMA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HIGH-TEMPERATURE WATER | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | HETEROGENEOUS ACID CATALYSIS | Polymerization | Biotechnology | Biomass | Biofuels | Cellulose | Energy consumption | High technology industry | Biomass energy | Peroxides | Nitrates | Nitrogen dioxide | Analysis
Cellulose oxidation | Biofuel | Depolymerisation | Energy conservation | PRIMARY ALCOHOL GROUPS | CARBON-SUPPORTED RUTHENIUM | TEMPO-MEDIATED OXIDATION | PINO RADICAL GENERATION | SOLID-ACID | SUPERCRITICAL WATER GASIFICATION | NONTHERMAL ATMOSPHERIC PLASMA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HIGH-TEMPERATURE WATER | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | HETEROGENEOUS ACID CATALYSIS | Polymerization | Biotechnology | Biomass | Biofuels | Cellulose | Energy consumption | High technology industry | Biomass energy | Peroxides | Nitrates | Nitrogen dioxide | Analysis
Journal Article
Synthesis, ISSN 0039-7881, 08/2013, Volume 45, Issue 15, pp. 2155 - 2164
Abstract Various benzylic and primary alcohols were efficiently converted into the corresponding nitriles in good yields at room temperature by treatment with...
paper | alcohols | nitriles | MOLECULAR-IODINE | SELECTIVE OXIDATION | CORRESPONDING NITRILES | COPPER-CATALYZED OXIDATION | LEAD TETRAACETATE | CHEMISTRY, ORGANIC | SECONDARY ALCOHOLS | ELECTRON-RICH AROMATICS | PRIMARY AMINES | DIRECT OXIDATIVE CONVERSION | FACILE PREPARATION
paper | alcohols | nitriles | MOLECULAR-IODINE | SELECTIVE OXIDATION | CORRESPONDING NITRILES | COPPER-CATALYZED OXIDATION | LEAD TETRAACETATE | CHEMISTRY, ORGANIC | SECONDARY ALCOHOLS | ELECTRON-RICH AROMATICS | PRIMARY AMINES | DIRECT OXIDATIVE CONVERSION | FACILE PREPARATION
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 03/2019, Volume 383, pp. 155 - 173
Nanotechnology fascinate the whole scientific community due to its huge impact on humans, since the derived products, i.e. nanoparticles (NPs), have a...
Nanoparticles | Gold nanoparticles | Silver nanoparticles | Cellulose | Magnetic nanoparticles | IRON-OXIDE NANOPARTICLES | ANTIMICROBIAL PROPERTIES | SUPPORTED GOLD NANOPARTICLES | BACTERIAL CELLULOSE | CHEMISTRY, INORGANIC & NUCLEAR | SILVER-NANOPARTICLES | ANTIBACTERIAL ACTIVITY | GREEN SYNTHESIS | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | IN-SITU SYNTHESIS
Nanoparticles | Gold nanoparticles | Silver nanoparticles | Cellulose | Magnetic nanoparticles | IRON-OXIDE NANOPARTICLES | ANTIMICROBIAL PROPERTIES | SUPPORTED GOLD NANOPARTICLES | BACTERIAL CELLULOSE | CHEMISTRY, INORGANIC & NUCLEAR | SILVER-NANOPARTICLES | ANTIBACTERIAL ACTIVITY | GREEN SYNTHESIS | HYDROXYPHTHALIMIDE (NHPI)/LEAD TETRAACETATE | IN-SITU SYNTHESIS
Journal Article
Organic Letters, ISSN 1523-7060, 09/2010, Volume 12, Issue 18, pp. 4066 - 4069
A simple and efficient method for the synthesis of 1,3,4-trisubstituted or 3,4-disubstituted pyrroles has been developed. The reaction represents the first...
OXIDATION | ENAMINE-ESTERS | SEQUENTIAL REACTIONS | EFFICIENT TOTAL-SYNTHESIS | LEAD-TETRAACETATE | ALPHA-ARYLATION | C BOND FORMATION | SUBSTITUTED PYRROLES | CHEMISTRY, ORGANIC | DIRECT ANNULATION | ALKALOIDS | Amines - chemistry | Pyrroles - chemical synthesis | Acetates - chemistry | Heterocyclic Compounds, 4 or More Rings - chemical synthesis | Molecular Structure | Dimerization | Silver Compounds - chemistry | Aldehydes - chemistry
OXIDATION | ENAMINE-ESTERS | SEQUENTIAL REACTIONS | EFFICIENT TOTAL-SYNTHESIS | LEAD-TETRAACETATE | ALPHA-ARYLATION | C BOND FORMATION | SUBSTITUTED PYRROLES | CHEMISTRY, ORGANIC | DIRECT ANNULATION | ALKALOIDS | Amines - chemistry | Pyrroles - chemical synthesis | Acetates - chemistry | Heterocyclic Compounds, 4 or More Rings - chemical synthesis | Molecular Structure | Dimerization | Silver Compounds - chemistry | Aldehydes - chemistry
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 11/2014, Volume 2014, Issue 31, pp. 6953 - 6962
The divergent synthesis of calothrixins and ellipticines has been accomplished by utilising the one‐pot formation of o‐diacylarenes as a key intermediate...
Quinones | Oxidation | Nitrogen heterocycles | Natural products | Rearrangement | ACTIVE CARBAZOLE ALKALOIDS | ORGANIC-SYNTHESIS | ROUTE | LEAD-TETRAACETATE | ENTRY | ANALOGS | CHEMISTRY, ORGANIC | CANCER | FACILE SYNTHESIS | DERIVATIVES
Quinones | Oxidation | Nitrogen heterocycles | Natural products | Rearrangement | ACTIVE CARBAZOLE ALKALOIDS | ORGANIC-SYNTHESIS | ROUTE | LEAD-TETRAACETATE | ENTRY | ANALOGS | CHEMISTRY, ORGANIC | CANCER | FACILE SYNTHESIS | DERIVATIVES
Journal Article