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2010, 2nd completely rev. and enl. ed., ISBN 3527322892, xi, 374
Gathering together the widespread literature in the field, this monograph acts as a reference guide to this very important chemical reaction. Following an... 
Esterification | Chemistry, Organic
Book
Journal of the American Chemical Society, ISSN 0002-7863, 10/2013, Volume 135, Issue 40, pp. 15257 - 15262
Journal Article
2003, ISBN 9783527304905, 315
Here, Professor J. Otera brings together for the first time the combined knowledge about this elementary yet multifaceted reaction. Starting from the... 
Esterification
eBook
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2012, Volume 51, Issue 2, pp. 314 - 325
Journal Article
by Du, BN and Wang, WM and Wang, Y and Qi, ZH and Tian, JQ and Zhou, J and Wang, XC and Han, JL and Ma, J and Pan, Y
CHEMISTRY-AN ASIAN JOURNAL, ISSN 1861-4728, 02/2018, Volume 13, Issue 4, pp. 404 - 408
A Cu-catalyzed cascade oxidative radical process of -keto sulfones with alcohols has been achieved by using oxygen as an oxidant. In this reaction, -keto... 
ORGANIC-SYNTHESIS | ACTIVATION | beta-keto sulfones | FUNCTIONALIZATIONS | CARBON-SULFUR | STRATEGY | aerobic oxidation | CHEMISTRY, MULTIDISCIPLINARY | C-S bond cleavage | CROSS-COUPLING REACTIONS | COOPERATIVE CATALYSIS | LIGHT PHOTOREDOX CATALYSIS | copper | density fuctional calculations | METAL-COMPLEXES | CYCLIZATION | Sulfur compounds | Copper | Bonds | Organic compounds
Journal Article
ChemCatChem, ISSN 1867-3880, 09/2017, Volume 9, Issue 17, pp. 3322 - 3329
The synthesis of 5,5′‐[oxybis(methylene)]bis‐2‐furfural (OBMF) from 5‐hydroxymethylfurfural (5‐HMF) was studied using bulk and alumina‐supported Preyssler... 
cluster compounds | acidity | heterogeneous catalysis | supported catalysts | molybdenum | OXIDATION | PHOSPHOTUNGSTIC ACID | ESTERIFICATION | CHEMISTRY, PHYSICAL | ALUMINA | CATALYTIC PERFORMANCE | BIOMASS | N-BUTANOL | CHEMISTRY | EFFICIENT | ANHYDRIDE | Aluminum compounds | Heterogeneous catalysis | Molybdenum
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2012, Volume 51, Issue 50, pp. 12570 - 12574
Clear cut: For the title reaction, O2, the ideal oxidant, was used as the only oxidizing reagent. The dimer intermediate (see scheme) and isotopic labeling... 
oxidation | CC bond cleavage | esterification | α‐hydroxy ketones | synthetic methods | C-C bond cleavage | α-hydroxy ketones | Transition Elements - chemistry | Oxygen Isotopes - chemistry | Oxidation-Reduction | Molecular Conformation | Ketones - chemistry | Isotope Labeling | Crystallography, X-Ray | Dimerization | Carbon - chemistry | Esterification
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 07/2017, Volume 359, Issue 14, pp. 2369 - 2374
The efficiency of N,N‐dimethylformamide (DMF) in the N‐heterocyclic carbene‐catalyzed Mannich reaction for the synthesis of β‐amino ketones has been... 
oxidation | N,N-dimethylformamide | 2-aminopyridines | β-amino ketones | Mannich reaction | N-heterocyclic carbenes | BRONSTED ACID | NHC | CHEMISTRY, ORGANIC | AROMATIC-ALDEHYDES | ALPHA-METHYLATION | NUCLEOPHILIC CARBENE | ESTERS | AEROBIC OXIDATION | CHEMISTRY, APPLIED | OXIDATIVE ESTERIFICATION | DMF | beta-amino ketones
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2019, Volume 58, Issue 38, pp. 13370 - 13374
While the enantioselective Rauhut–Currier reaction is established with bis(enone) substrates, it is yet to be reported with less electrophilic bis(enoate)... 
bis(enoate)s | coumarins | enantioselective catalysis | Rauhut–Currier reaction | N-heterocyclic carbenes | TO-TAIL DIMERIZATION | ANNULATION | ORGANOCATALYSIS | CHEMISTRY, MULTIDISCIPLINARY | Rauhut-Currier reaction | NUCLEOPHILICITY | SCAFFOLDS | UMPOLUNG | HYDROACYLATION | Coumarins | Enantiomers | Catalysis | Carbenes | Cascades | Substrates | Esterification
Journal Article
Fuel Processing Technology, ISSN 0378-3820, 01/2017, Volume 155, pp. 2 - 19
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 1, pp. 338 - 342
Naphthols and 3‐trifluoroethylidene oxindoles were found to undergo an asymmetric Friedel–Crafts alkylation/lactonization reaction, catalyzed by only 2.5 mol %... 
organocatalysis | amides | arenes | heterocycles | synthetic methods | CATALYSIS | ACTIVATION | ACID | ALKYLATION | O-QUINONE METHIDES | CASCADE | IDENTIFICATION | CHEMISTRY, MULTIDISCIPLINARY | ANTICANCER POTENCY | CHEMISTRY | DERIVATIVES | Amides | Synthesis | Catalysis | Organic compounds | Asymmetric synthesis | Aromatic compounds | Naphthol | Crafts | Chemical synthesis | Quinine | Esterification | Alkylation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2008, Volume 48, Issue 1, pp. 168 - 171
Journal Article