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Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 34, pp. 9984 - 9987
An adhesive yet easily removable burn wound dressing represents a breakthrough in second‐degree burn wound care. Current second‐degree burn wound dressings... 
wound dressing | thiol–thioester exchange | dendrimers | hydrogel | dissolution | DESIGN | thiol-thioester exchange | PAIN | CHEMISTRY, MULTIDISCIPLINARY | Dendrimers | Burns and scalds | Care and treatment | Thiols | Bacterial infections | Lysine | Analysis | Wounds and injuries | Hydrogels | Medical supplies | Dissolution
Journal Article
Macromolecular Chemistry and Physics, ISSN 1022-1352, 08/2018, Volume 219, Issue 16, pp. 1800177 - n/a
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 12/2017, Volume 359, Issue 24, pp. 4405 - 4410
We report a direct synthesis of 2‐thioxooxazolidin‐4‐ones and oxazolidine‐2,4‐diones from α‐keto thioesters with sodium thiocyanate or potassium cyanate,... 
α-keto thioesters | 2-thioxooxazolidin-4-ones | oxazolidine-2,4-diones | rearrangement | synthetic methods | SULFIDES | EXPEDIENT SYNTHESIS | CHEMISTRY, ORGANIC | PPH3-CENTER-DOT-HBR-DMSO | POTASSIUM CYANATE | alpha-keto thioesters | POTENT | HETEROCYCLES | ARYL HALIDES | INHIBITORS | CHEMISTRY, APPLIED | MIGRATIONS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2018, Volume 57, Issue 22, pp. 6653 - 6657
Insertion of tert‐butyl isocyanide into the C(sp2)−S bonds of heteroaryl sulfides is catalyzed by a palladium diphosphine complex. Thioimidates generated... 
palladium | isocyanides | heterocycles | thioesters | synthetic methods | ACTIVATION | ACID | RING-EXPANSION | ARYL SULFIDES | palladium thioesters | THIOL ESTERS | CHEMISTRY, MULTIDISCIPLINARY | THIOCARBONYLATION | CARBON-MONOXIDE | SILICON-SILICON | METAL | REGIOSPECIFIC CARBONYLATION | Sulfides | Palladium | Insertion | Thioesters | Sulfur
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 08/2017, Volume 359, Issue 15, pp. 2692 - 2698
α‐Keto thioesters, with two electrophilic carbon centres, have been found to react differently with β‐keto esters and isocyanoacetates. They undergo base... 
oxazoles | α-keto thioesters | γ-hydroxybutenolides | synthetic methods | rearrangement | ACIDS | ANNULATION | SUBSTITUTED BUTENOLIDES | REACTIVITY | CHEMISTRY, ORGANIC | PPH3-CENTER-DOT-HBR-DMSO | CYCLOADDITION | alpha-keto thioesters | gamma-hydroxybutenolides | CHEMISTRY | INHIBITORS | CHEMISTRY, APPLIED | DERIVATIVES | AQUEOUS SOLUBILITY
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 01/2017, Volume 58, Issue 3, pp. 185 - 189
[Display omitted] •Direct aldol addition.•Soft enolization.•Syn-selective aldol.•Kinetically controlled soft enolization process. Herein we report that simple... 
Kinetic control | α-Halo-β-hydroxy thioester | Thioester | Soft enolization | Direct aldol addition | 1,3-DIKETONES | ACIDS | CHEMISTRY, ORGANIC | DARZENS REACTION | ALDEHYDES | CARBON BOND FORMATION | TRIETHYLAMINE | KETONES | alpha-Halo-beta-hydroxy thioester | ESTERS | FACILE
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 03/1995, Volume 92, Issue 7, pp. 2563 - 2567
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2019, Volume 55, Issue 13, pp. 1907 - 1910
A method for Ni-catalyzed controlled decarbonylation of α-ketothioesters is described. Mono- and double-decarbonylations, which gave thioesters and thioethers,... 
Thioesters | Nuclear magnetic resonance--NMR
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2016, Volume 55, Issue 13, pp. 4275 - 4279
To integrate anion–π, cation–π, and ion pair–π interactions in catalysis, the fundamental challenge is to run reactions reliably on aromatic surfaces.... 
selectivity | catalysis | enolates | anion–π interactions | preorganization | anion-π interactions | Organic chemistry | Anions | Thioesters | Catalysis | Rigidity | Substrates | Intermediates
Journal Article