Thioesters as Acyl Donors in Biocatalytic Friedel-Crafts-type Acylation Catalyzed by Acyltransferase from Pseudomonas Protegens
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Thioesters as Acyl Donors in Biocatalytic Friedel-Crafts-type Acylation Catalyzed by Acyltransferase from Pseudomonas Protegens
Authors
Keywords
-
Journal
ChemCatChem
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-01-09
DOI
10.1002/cctc.201801856
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Complete Switch of Reaction Specificity of an Aldolase by Directed Evolution In Vitro: Synthesis of Generic Aliphatic Aldol Products
- (2018) Sebastian Junker et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Synthesis of Branched-Chain Sugars with a DHAP-Dependent Aldolase: Ketones are Electrophile Substrates of Rhamnulose-1-phosphate Aldolases
- (2018) Victor Laurent et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Promiscuous activity of C-acyltransferase from Pseudomonas protegens: synthesis of acetanilides in aqueous buffer
- (2018) Anna Żądło-Dobrowolska et al. CHEMICAL COMMUNICATIONS
- Friedel-Crafts reactions in aqueous media and their synthetic applications
- (2018) Zubi Sadiq et al. JOURNAL OF MOLECULAR LIQUIDS
- C–H carbonylation: In situ acyl triflates ace it
- (2018) Yong Ho Lee et al. Nature Chemistry
- Acyl Donors and Additives for the Biocatalytic Friedel-Crafts Acylation
- (2017) Nina G. Schmidt et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Zeolite catalyzed highly selective synthesis of 2-methoxy-6-acetylnaphthalene by Friedel-Crafts acylation of 2-methoxynaphthalene in acetic acid reaction media
- (2017) Tomoyoshi Yamazaki et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Distribution of 2,4-Diacetylphloroglucinol Biosynthetic Genes among the Pseudomonas spp. Reveals Unexpected Polyphyletism
- (2017) Juliana Almario et al. Frontiers in Microbiology
- A Continuous-Flow Cascade Reactor System for Subtilisin A- Catalyzed Dynamic Kinetic Resolution ofN-tert-Butyloxycarbonylphenylalanine Ethyl Thioester with Benzylamine
- (2016) Péter Falus et al. ADVANCED SYNTHESIS & CATALYSIS
- Natural products as sources of new fungicides (III): Antifungal activity of 2,4-dihydroxy-5-methylacetophenone derivatives
- (2016) Wei Shi et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Sterically-controlled intermolecular Friedel–Crafts acylation with twisted amides via selective N–C cleavage under mild conditions
- (2016) Yongmei Liu et al. CHEMICAL COMMUNICATIONS
- Effect of Additives on the Selectivity and Reactivity of Enzymes
- (2016) Yi-Ru Liang et al. CHEMICAL RECORD
- Hexafluoro-2-propanol-Promoted Intermolecular Friedel–Crafts Acylation Reaction
- (2016) Rakesh H. Vekariya et al. ORGANIC LETTERS
- Using mutability landscapes of a promiscuous tautomerase to guide the engineering of enantioselective Michaelases
- (2016) Jan-Ytzen van der Meer et al. Nature Communications
- Building Bridges: Biocatalytic C–C-Bond Formation toward Multifunctional Products
- (2016) Nina G. Schmidt et al. ACS Catalysis
- Mesopore wall-catalyzed Friedel–Crafts acylation of bulky aromatic compounds in MFI zeolite nanosponge
- (2015) Jeong-Chul Kim et al. CATALYSIS TODAY
- [Bmim]2SbCl5: a main group metal-containing ionic liquid exhibiting tunable photoluminescence and white-light emission
- (2015) Ze-Ping Wang et al. CHEMICAL COMMUNICATIONS
- Catalytic, Green and Regioselective Friedel-Crafts Acylation of Simple Aromatics and Heterocycles Over Zeolites
- (2015) Gamal A. El-Hiti et al. CURRENT ORGANIC CHEMISTRY
- One-pot triangular chemoenzymatic cascades for the syntheses of chiral alkaloids from dopamine
- (2015) B. R. Lichman et al. GREEN CHEMISTRY
- Graphene-Catalyzed Direct Friedel–Crafts Alkylation Reactions: Mechanism, Selectivity, and Synthetic Utility
- (2015) Feng Hu et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Asymmetric assembly of aldose carbohydrates from formaldehyde and glycolaldehyde by tandem biocatalytic aldol reactions
- (2015) Anna Szekrenyi et al. Nature Chemistry
- Catalyst-free direct decarboxylative coupling of α-keto acids with thiols: a facile access to thioesters
- (2015) Kelu Yan et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Stereoselective Mannich Reaction ofS-Phenyl Thioesters Catalyzed by Bifunctional Organocatalysts
- (2014) Jie Guang et al. ADVANCED SYNTHESIS & CATALYSIS
- Palladium-Catalyzed Thiocarbonylation of Aryl, Vinyl, and Benzyl Bromides
- (2014) Mia N. Burhardt et al. JOURNAL OF ORGANIC CHEMISTRY
- Biocatalytic Methods for CC Bond Formation
- (2013) Kateryna Fesko et al. ChemCatChem
- Combinatorial Synthesis and in Vitro Evaluation of a Biaryl Hydroxyketone Library as Antivirulence Agents against MRSA
- (2013) Guanping Yu et al. ACS Combinatorial Science
- Recent Developments in Enzymatic Asymmetric CC Bond Formation
- (2012) Michael Müller ADVANCED SYNTHESIS & CATALYSIS
- Molecular and Catalytic Properties of Monoacetylphloroglucinol Acetyltransferase fromPseudomonassp. YGJ3
- (2012) Asuka HAYASHI et al. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
- L-Amino Acid Amides via Dynamic Kinetic Resolution
- (2011) Davide Tessaro et al. ADVANCED SYNTHESIS & CATALYSIS
- Biosynthesis of phloroglucinol compounds in microorganisms—review
- (2011) Fang Yang et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Modulating the synthetase activity of penicillin G acylase in organic media by addition of N-methylimidazole: Using vinyl acetate as activated acyl donor
- (2011) Bokai Liu et al. JOURNAL OF BIOTECHNOLOGY
- A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis
- (2010) Magnus Rueping et al. Beilstein Journal of Organic Chemistry
- Cleaner Routes for Friedel-Crafts Acylation
- (2010) Nicolas Aribert et al. International Journal of Chemical Reactor Engineering
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started