Research graph
References from Biocatalytic Synthesis of Substituted Cinnamaldehydes. Local targets link to admitted publications; unresolved targets remain external evidence.
Cinnamomum cassia Presl: A Review of Its Traditional Uses, Phytochemistry, Pharmacology and Toxicology
10.3390/molecules24193473 · 2019 · External reference
Cinnamaldehyde in Focus: Antimicrobial Properties, Biosynthetic Pathway, and Industrial Applications
10.3390/antibiotics13111095 · 2024 · External reference
Advances in pharmacological effects and mechanism of action of cinnamaldehyde
10.3389/fphar.2024.1365949 · 2024 · External reference
Cinnamon: The historic spice, medicinal uses, and flavour chemistry
10.1016/j.ijgfs.2023.100858 · 2024 · External reference
Boosting multiple photo-assisted and temperature controlled reactions with a single redox-switchable catalyst: Solvents as internal substrates and reducing agent
10.1016/j.jcat.2020.04.026 · 2020 · External reference
One-Pot Preparation of (E)-α,β-Unsaturated Aldehydes by a Julia–Kocienski Reaction of 2,2-Dimethoxyethyl PT Sulfone Followed by Acid Hydrolysis
10.1021/acs.joc.1c00479 · 2021 · External reference
Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N-Diisopropylethylamine and 1,1,1,3,3,3-Hexafluoropropan-2-ol
10.1002/celc.202000275 · 2020 · External reference
Oxidative Coupling of Benzenes with α,β-Unsaturated Aldehydes by the Pd(OAc)2/Molybdovanadophosphoric Acid/O2 System
10.1021/jo050534o · 2005 · External reference
Rare earth triflates/chlorotrimethylsilane induced activation of triethylamine as a latent acetaldehyde anion: a new synthesis of α,β-unsaturated aldehydes
10.1016/j.tetlet.2009.11.014 · 2010 · External reference
Synthesis of Functionalized Cinnamaldehyde Derivatives by an Oxidative Heck Reaction and Their Use as Starting Materials for Preparation of Mycobacterium tuberculosis 1-Deoxy-d-xylulose-5-phosphate Reductoisomerase Inhibitors
10.1021/jo201715x · 2011 · External reference
De novo biosynthesis of trans-cinnamic acid derivatives in Saccharomyces cerevisiae
10.1007/s00253-017-8220-x · 2017 · External reference
Production of Cinnamaldehyde through Whole-Cell Bioconversion from trans-Cinnamic Acid Using Engineered Corynebacterium glutamicum
10.1021/acs.jafc.1c07398 · 2022 · External reference
Systematic metabolic engineering of Escherichia coli for the enhanced production of cinnamaldehyde
10.1016/j.ymben.2023.01.006 · 2023 · External reference
Biocatalysis: A smart and green tool for the preparation of chiral drugs
10.1002/chir.23498 · 2022 · External reference
Design of an in vitro biocatalytic cascade for the manufacture of islatravir
10.1126/science.aay8484 · 2019 · External reference
Development of a Biocatalytic Aerobic Oxidation for the Manufacturing Route to Islatravir
10.1021/acs.oprd.4c00075 · 2024 · External reference
Biocatalytic Synthesis of α,β-Unsaturated 2-Keto Acids and Derivatives Using the Promiscuous Aldolase, NahE
10.1055/a-1953-1509 · 2023 · External reference
Substrate specificity in thiamin diphosphate-dependent decarboxylases
10.1016/j.bioorg.2011.12.001 · 2012 · External reference
The Ehrlich Pathway for Fusel Alcohol Production: a Century of Research on Saccharomyces cerevisiae Metabolism
10.1128/aem.02625-07 · 2008 · External reference
Characterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from Saccharomyces cerevisiae
10.1111/j.1742-4658.2011.08103.x · 2011 · External reference
Identification, cloning, and characterization of a Lactococcus lactis branched-chain α-keto acid decarboxylase involved in flavor formation
10.1128/aem.71.1.303-311.2005 · 2005 · External reference
Crystal structure of thiamindiphosphate-dependent indolepyruvate decarboxylase from Enterobacter cloacae, an enzyme involved in the biosynthesis of the plant hormone indole-3-acetic acid
10.1046/j.1432-1033.2003.03601.x · 2003 · External reference
Mandelate pathway of Pseudomonas putida: sequence relationships involving mandelate racemase, (S)-mandelate dehydrogenase, and benzoylformate decarboxylase and expression of benzoylformate decarboxylase in Escherichia coli
10.1021/bi00494a015 · 1990 · External reference
Identification, Cloning, and Characterization of a Lactococcus lactis Branched-Chain α-Keto Acid Decarboxylase Involved in Flavor Formation
10.1128/aem.71.1.303-311.2005 · 2005 · External reference
IAA Producing Enterobacter sp. I-3 as a Potent Bio-herbicide Candidate for Weed Control: A Special Reference with Lettuce Growth Inhibition
10.1007/s12088-015-0515-y · 2015 · External reference
Synthesis of the enzymes of the mandelate pathway by Pseudomonas putida. I. Synthesis of enzymes by the wild type
10.1128/jb.91.3.1140-1154.1966 · 1966 · External reference
Structural and kinetic analysis of catalysis by a thiamin diphosphate-dependent enzyme, benzoylformate decarboxylase
10.1021/bi026490k · 2003 · External reference
Comparative assessment of native and heterologous 2-oxo acid decarboxylases for application in isobutanol production by Saccharomyces cerevisiae
10.1186/s13068-015-0374-0 · 2015 · External reference
Branched-chain keto acid decarboxylase from Lactococcus lactis (KdcA), a valuable thiamine diphosphate-dependent enzyme for asymmetric C - C bond formation
10.1002/adsc.200700057 · 2007 · External reference
Development of a Donor–Acceptor Concept for Enzymatic Cross-Coupling Reactions of Aldehydes: The First Asymmetric Cross-Benzoin Condensation
10.1021/ja0271476 · 2002 · External reference
Alteration of the substrate specificity of benzoylformate decarboxylase from Pseudomonas putida by directed evolution
10.1002/cbic.200200475 · 2003 · External reference
Asymmetric Synthesis of Aliphatic 2-Hydroxy Ketones by Enzymatic Carboligation of Aldehydes
10.1002/ejoc.200600876 · 2007 · External reference
Studies on structure-function relationships of indolepyruvate decarboxylase from Enterobacter cloacae, a key enzyme of the indole acetic acid pathway
10.1046/j.1432-1033.2003.03602.x · 2003 · External reference
Engineering phenylpyruvate decarboxylase for controlled biosynthesis of aromatic amino acid derivatives
10.1016/j.ymben.2025.07.001 · 2025 · External reference
An enzymatic approach to the synthesis of optically pure (3R)- and (3S)-enantiomers of green tea flavor compound 3-hydroxy-3-methylnonane-2,4-dione
10.1016/j.molcatb.2012.08.015 · 2013 · External reference
Constructing a synthetic pathway for acetyl-coenzyme A from one-carbon through enzyme design
10.1038/s41467-019-09095-z · 2019 · External reference
Folding and stability of different oligomeric states of thiamin diphosphate dependent homomeric pyruvate decarboxylase
10.1016/s0301-4622(02)00017-0 · 2002 · External reference
Comparison of substrate specificity of alcohol dehydrogenases from human liver, horse liver, and yeast towards saturated and 2-enoic alcohols and aldehydes
10.1016/0003-9861(73)90428-1 · 1973 · External reference
Biochemical and Structural Insights into a Thiamine Diphosphate-Dependent α-Ketoglutarate Decarboxylase from Cyanobacterium Microcystis aeruginosa NIES-843
10.3390/ijms241512198 · 2023 · External reference
Kinetics and mechanism of benzoylformate decarboxylase using carbon-13 and solvent deuterium isotope effects on benzoylformate and benzoylformate analogs
10.1021/bi00406a058 · 1988 · External reference
Benzoylformate Decarboxylase from Pseudomonas putida as Stable Catalyst for the Synthesis of Chiral 2-Hydroxy Ketones
10.1002/(sici)1521-3765(20000417)6:8<1483::aid-chem1483>3.0.co;2-s · 2000 · External reference
Exchanging the substrate specificities of pyruvate decarboxylase from Zymomonas mobilis and benzoylformate decarboxylase from Pseudomonas putida
10.1093/protein/gzi035 · 2005 · External reference
Benzoylformate Decarboxylase from Pseudomonas putida as Stable Catalyst for the Synthesis of Chiral 2-Hydroxy Ketones
10.1002/(sici)1521-3765(20000417)6:8<1483::aid-chem1483>3.0.co;2-s · ExternalCitation · doi-reference
Branched-chain keto acid decarboxylase from Lactococcus lactis (KdcA), a valuable thiamine diphosphate-dependent enzyme for asymmetric C - C bond formation
10.1002/adsc.200700057 · ExternalCitation · doi-reference
Alteration of the substrate specificity of benzoylformate decarboxylase from Pseudomonas putida by directed evolution
10.1002/cbic.200200475 · ExternalCitation · doi-reference
Electrochemical Formation of Cinnamaldehyde by the Electrolyte System N,N-Diisopropylethylamine and 1,1,1,3,3,3-Hexafluoropropan-2-ol
10.1002/celc.202000275 · ExternalCitation · doi-reference
Biocatalysis: A smart and green tool for the preparation of chiral drugs
10.1002/chir.23498 · ExternalCitation · doi-reference
Asymmetric Synthesis of Aliphatic 2-Hydroxy Ketones by Enzymatic Carboligation of Aldehydes
10.1002/ejoc.200600876 · ExternalCitation · doi-reference
De novo biosynthesis of trans-cinnamic acid derivatives in Saccharomyces cerevisiae
10.1007/s00253-017-8220-x · ExternalCitation · doi-reference
IAA Producing Enterobacter sp. I-3 as a Potent Bio-herbicide Candidate for Weed Control: A Special Reference with Lettuce Growth Inhibition
10.1007/s12088-015-0515-y · ExternalCitation · doi-reference
Comparison of substrate specificity of alcohol dehydrogenases from human liver, horse liver, and yeast towards saturated and 2-enoic alcohols and aldehydes
10.1016/0003-9861(73)90428-1 · ExternalCitation · doi-reference
Substrate specificity in thiamin diphosphate-dependent decarboxylases
10.1016/j.bioorg.2011.12.001 · ExternalCitation · doi-reference
Cinnamon: The historic spice, medicinal uses, and flavour chemistry
10.1016/j.ijgfs.2023.100858 · ExternalCitation · doi-reference
Boosting multiple photo-assisted and temperature controlled reactions with a single redox-switchable catalyst: Solvents as internal substrates and reducing agent
10.1016/j.jcat.2020.04.026 · ExternalCitation · doi-reference
An enzymatic approach to the synthesis of optically pure (3R)- and (3S)-enantiomers of green tea flavor compound 3-hydroxy-3-methylnonane-2,4-dione
10.1016/j.molcatb.2012.08.015 · ExternalCitation · doi-reference
Rare earth triflates/chlorotrimethylsilane induced activation of triethylamine as a latent acetaldehyde anion: a new synthesis of α,β-unsaturated aldehydes
10.1016/j.tetlet.2009.11.014 · ExternalCitation · doi-reference
Systematic metabolic engineering of Escherichia coli for the enhanced production of cinnamaldehyde
10.1016/j.ymben.2023.01.006 · ExternalCitation · doi-reference
Engineering phenylpyruvate decarboxylase for controlled biosynthesis of aromatic amino acid derivatives
10.1016/j.ymben.2025.07.001 · ExternalCitation · doi-reference
Folding and stability of different oligomeric states of thiamin diphosphate dependent homomeric pyruvate decarboxylase
10.1016/s0301-4622(02)00017-0 · ExternalCitation · doi-reference
Production of Cinnamaldehyde through Whole-Cell Bioconversion from trans-Cinnamic Acid Using Engineered Corynebacterium glutamicum
10.1021/acs.jafc.1c07398 · ExternalCitation · doi-reference
One-Pot Preparation of (E)-α,β-Unsaturated Aldehydes by a Julia–Kocienski Reaction of 2,2-Dimethoxyethyl PT Sulfone Followed by Acid Hydrolysis
10.1021/acs.joc.1c00479 · ExternalCitation · doi-reference
Development of a Biocatalytic Aerobic Oxidation for the Manufacturing Route to Islatravir
10.1021/acs.oprd.4c00075 · ExternalCitation · doi-reference
Kinetics and mechanism of benzoylformate decarboxylase using carbon-13 and solvent deuterium isotope effects on benzoylformate and benzoylformate analogs
10.1021/bi00406a058 · ExternalCitation · doi-reference
Mandelate pathway of Pseudomonas putida: sequence relationships involving mandelate racemase, (S)-mandelate dehydrogenase, and benzoylformate decarboxylase and expression of benzoylformate decarboxylase in Escherichia coli
10.1021/bi00494a015 · ExternalCitation · doi-reference
Structural and kinetic analysis of catalysis by a thiamin diphosphate-dependent enzyme, benzoylformate decarboxylase
10.1021/bi026490k · ExternalCitation · doi-reference
Development of a Donor–Acceptor Concept for Enzymatic Cross-Coupling Reactions of Aldehydes: The First Asymmetric Cross-Benzoin Condensation
10.1021/ja0271476 · ExternalCitation · doi-reference
Oxidative Coupling of Benzenes with α,β-Unsaturated Aldehydes by the Pd(OAc)2/Molybdovanadophosphoric Acid/O2 System
10.1021/jo050534o · ExternalCitation · doi-reference
Synthesis of Functionalized Cinnamaldehyde Derivatives by an Oxidative Heck Reaction and Their Use as Starting Materials for Preparation of Mycobacterium tuberculosis 1-Deoxy-d-xylulose-5-phosphate Reductoisomerase Inhibitors
10.1021/jo201715x · ExternalCitation · doi-reference
Constructing a synthetic pathway for acetyl-coenzyme A from one-carbon through enzyme design
10.1038/s41467-019-09095-z · ExternalCitation · doi-reference
Crystal structure of thiamindiphosphate-dependent indolepyruvate decarboxylase from Enterobacter cloacae, an enzyme involved in the biosynthesis of the plant hormone indole-3-acetic acid
10.1046/j.1432-1033.2003.03601.x · ExternalCitation · doi-reference
Studies on structure-function relationships of indolepyruvate decarboxylase from Enterobacter cloacae, a key enzyme of the indole acetic acid pathway
10.1046/j.1432-1033.2003.03602.x · ExternalCitation · doi-reference
Biocatalytic Synthesis of α,β-Unsaturated 2-Keto Acids and Derivatives Using the Promiscuous Aldolase, NahE
10.1055/a-1953-1509 · ExternalCitation · doi-reference
Exchanging the substrate specificities of pyruvate decarboxylase from Zymomonas mobilis and benzoylformate decarboxylase from Pseudomonas putida
10.1093/protein/gzi035 · ExternalCitation · doi-reference
Characterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from Saccharomyces cerevisiae
10.1111/j.1742-4658.2011.08103.x · ExternalCitation · doi-reference
Design of an in vitro biocatalytic cascade for the manufacture of islatravir
10.1126/science.aay8484 · ExternalCitation · doi-reference
The Ehrlich Pathway for Fusel Alcohol Production: a Century of Research on Saccharomyces cerevisiae Metabolism
10.1128/aem.02625-07 · ExternalCitation · doi-reference
Identification, Cloning, and Characterization of a Lactococcus lactis Branched-Chain α-Keto Acid Decarboxylase Involved in Flavor Formation
10.1128/aem.71.1.303-311.2005 · ExternalCitation · doi-reference
Synthesis of the enzymes of the mandelate pathway by Pseudomonas putida. I. Synthesis of enzymes by the wild type
10.1128/jb.91.3.1140-1154.1966 · ExternalCitation · doi-reference
Comparative assessment of native and heterologous 2-oxo acid decarboxylases for application in isobutanol production by Saccharomyces cerevisiae
10.1186/s13068-015-0374-0 · ExternalCitation · doi-reference
Advances in pharmacological effects and mechanism of action of cinnamaldehyde
10.3389/fphar.2024.1365949 · ExternalCitation · doi-reference
Cinnamaldehyde in Focus: Antimicrobial Properties, Biosynthetic Pathway, and Industrial Applications
10.3390/antibiotics13111095 · ExternalCitation · doi-reference
Biochemical and Structural Insights into a Thiamine Diphosphate-Dependent α-Ketoglutarate Decarboxylase from Cyanobacterium Microcystis aeruginosa NIES-843
10.3390/ijms241512198 · ExternalCitation · doi-reference
Cinnamomum cassia Presl: A Review of Its Traditional Uses, Phytochemistry, Pharmacology and Toxicology
10.3390/molecules24193473 · ExternalCitation · doi-reference
