Multienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid
Di Gennaro, Patrizia
Bernasconi, Silvana
Orsini, Fulvia
Corretto, Erika
Sello, Guido
Tetrahedron Asymmetry, 2010
GUIDO GIOVANNI SELLO
SELLO GUIDO GIOVANNI
ORCID: 0000-0003-2538-9107
Natural stilbenes and analogues as antineoplastic agents
10.1016/s1572-5995(08)80025-7
Question of data format in organic chemistry
10.1021/ci00044a011
Residual charges on atoms in organic structures: A new algorithm for their calculation
10.1016/0898-5529(89)90027-4
Residual charges on atoms in organic structures: A new method for the identification of conjugated systems and the evaluation of atomic charge distribution on them
10.1016/0898-5529(89)90011-0
Residual charges on atoms in organic structures: Molecules containing charged and backdonating atoms
10.1016/0898-5529(89)90012-2
Carcinogenicity prediction of noncongeneric chemicals by augmented top priority fragment classification
10.1016/j.compbiolchem.2016.01.011
From dioxin to dioxin congeners: understanding the differences in hydrophobic aggregation in water and absorption into lipid membranes by means of atomistic simulations
10.1039/c6cp01728b
Hydrophobic aggregation and collective absorption of dioxin into lipid membranes: insights from atomistic simulations
10.1039/c4cp05466k
Aldol Reactions of the trans-o-Hydroxybenzylidenepyruvate Hydratase-Aldolase (tHBP-HA) from Pseudomonas fluorescens N3
10.1007/s12010-013-0302-3
Determination of Toxicant Mode of Action by Augmented Top Priority Fragment Class
10.1021/ci400130n
Regulated expression systems for the development of whole-cell biocatalysts expressing oxidative enzymes in a sequential manner
10.1007/s00203-013-0875-9
Characterization of the aldol condensation activity of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) cloned from Pseudomonas fluorescens N3
10.1016/j.bbapap.2011.03.013
Identification of Toxifying and Detoxifying Moieties for Mutagenicity Prediction by Priority Assessment
10.1021/ci200075g
Microbial enzymes for aromatic compound hydroxylation
10.1007/s00253-011-3285-4
Development of regulated systems for the expression of oxidoreductive enzymes from Pseudomonas and their use in sequential biotransformations
10.1016/j.jbiotec.2010.09.531
Multienzymatic preparation of 3- (1R)-1-hydroxyethylibenzoic acid and (2S)-hydroxy(phenyl)ethanoic acid
10.1016/j.tetasy.2010.07.007
Multienzymatic preparation of (-)- 3-(oxiran-2-yl)phenyl methanol and (-)-3-(oxiran-2-yl)benzoic acid
10.1016/j.tetasy.2009.03.023
One-Pot, Fluoride-Promoted Wittig Reaction
10.1080/00397910802654633
Use of oxidoreductive enzymes in sequential biotransformations
10.1016/j.nbt.2009.06.394
Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions
10.1016/j.molcatb.2007.10.014
Definition and detection of outliers in chemical space
10.1021/ci7004065
Novel auto-inducing expression systems for the development of whole-cell biocatalysts
10.1007/s00253-008-1460-z
Insect pest control agents: Novel chiral butanoate esters (juvenogens)
10.1016/j.bmc-2007.06.043
Isolation, cloning and synthetic use of the tHBP aldolase from Pseudomonas fluorescens N3
10.1016/j.jbiotec.2007.07.177
Styrene lower catabolic pathway in Pseudomonas fluorescens ST: identification and characterization of genes for phenylacetic acid degradation
10.1007/s00203-007-0226-9
Alcohol and 1,2-diol dehydrogenases: Synthetic use as oxidants
10.2174/157019306775474167
Alcohol and 1,2-diol dehydrogenases: Synthetic use in the preparation of chiral alcohols by carbonyl reduction
10.2174/157019306775474185
Dioxygenation of naphthalene by Pseudomonas fluorescens N3 dioxygenase: Optimization of the process parameters
10.1002/bit.20736
One-pot Wittig reactions in water and in the presence of a surfactant
10.1055/s-2006-947323
Recent developments in epoxide preparation
10.2174/157017906778699503
Selective enzymatic reduction of aldehydes
10.3390/11050365
Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis
10.1016/j.tetasy.2006.01.009
Top-priority fragment QSAR approach in predicting pesticide aquatic toxicity
10.1021/tx0601814
(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric Reformatsky reactions
10.1016/j.tetasy.2005.04.008
An automated group contribution method in predicting aquatic toxicity: The diatomic fragment approach
10.1021/tx049665v
Electroreduction of volatile organic halides on activated silver cathodes
10.1007/s10800-005-0798-5
Quantitative aquatic toxicity prediction: using group contribution and classification methods on polar and non-polar narcotics
10.1016/j.theochem.2005.02.035
Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: study of the effects of substituent nature and position
10.1016/j.tetasy.2004.04.005
Characterization of styrene catabolic pathway in Pseudomonas fluorescens ST
10.1016/j.ibiod.2004.06.005
Chemoenzymatic synthesis of conduritol analogues
10.1016/j.tetlet.2004.10.072
Formation of bound residues by naphthalene and cis-naphthalene-1,2-dihydrodiol
10.1016/j.chemosphere.2004.04.017
Organic phase effect in the biphasic bioconversion of substituted naphthalenes by engineered E-coli containing P-fluorescens N3 dioxygenase
10.1016/j.molcatb.2003.10.013
Preparation and synthetic use of enantiopure naphthalene dihydrodiols
10.2174/1570193043488944
Transition metals-mediated Reformatsky reactions
10.2174/1570179043485385
A chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralins
10.1016/s0957-4166(02)00098-8
Characterization of Rhodococcus opacus R7, a strain able to degrade naphthalene and o-xylene isolated from a polycyclic aromatic hydrocarbon-contaminated soil
10.1016/s0923-2508(01)01243-8
Enantiopure vic-amino alcohols and vic-diamines from (1R,2S)-1,2-dihydroxy-1,2-dihydronaphthalene
10.1016/s0957-4166(01)00510-9
Organization and regulation of meta cleavage pathway genes for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1
10.1128/aem.67.7.3304-3308.2001
Predicting toxicity: a mechanism of action model of chemical mutagenicity
10.1016/s0027-5107(01)00161-0
Silver as a powerful electrocatalyst for organic halide reduction: the critical role of molecular structure
10.1016/s0013-4686(01)00616-8
Bioconversion of substituted styrenes to the corresponding enantiomerically pure epoxides by a recombinant Escherichia coli strain
10.1016/s0040-4039(00)01639-7
Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions
10.1016/s0923-2508(00)00161-3
Electrocatalytic potentialities of silver as a cathode for organic halide reductions
10.1016/s1388-2481(00)00065-5
Prediction of organic reaction products: Determining the best reaction conditions
10.1021/ci990430c
Reaction centre accessibility. I. Calculation of reaction centre congestion and influence of structure flexibility
10.1016/s0097-8485(00)00068-1
Reaction centre accessibility. II. Role of reaction centre congestion in the calculation of reaction centre accessibility
10.1016/s0097-8485(00)00069-3
Reactivity of halo sugars on silver cathodes
10.1135/cccc20000881
1,2-dihydro-1,2-dihydroxynaphthalene dehydrogenase containing recombinant strains: Preparation, isolation and characterisation of 1,2-dihydroxynaphthalenes and 1,2-naphthoquinones
10.1016/s0040-4020(99)00135-0
Cathode and medium effects on the electroreductive glucosidation of phenols
10.1039/a901329f
Glycosyl halides as building blocks for the electrosynthesis of glycosides
10.1149/1.1838424
Reaction classification by similarity: the influence of steric congestion
10.1016/s0040-4020(98)00261-0
Similarity measures: Is it possible to compare dissimilar structures?
10.1021/ci980180k
Synthetic approach to Kdo glycosides via exo-glycal epoxides and rationalization of the stereochemical outcome
10.1080/07328309808001899
Bioconversion of substituted naphthalenes to the corresponding 1,2-dihydroxy derivatives by Escherichia coli recombinant strains
10.1016/s0040-4039(97)01404-4
Classification of organic reactions using similarity
10.1016/s0040-4020(97)00911-3
Organic synthesis planning: Some hints from similarity
10.1016/s0040-4020(97)00095-1
Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3
10.1016/s0923-2508(97)81591-4
Specificity of substrate recognition by Pseudomonas fluorescens N3 dioxygenase - The role of the oxidation potential and molecular geometry
10.1074/jbc.272.48.30254
Analysis of a theoretical model based on similarity for studying RNA base pairings
10.1006/jtbi.1996.0137
Design of beta-amino alcohols as chiral auxiliaries in the electrophilic amination of 1,3,2-oxazaphospholanes
10.1016/0040-4020(96)00839-3
Microbial oxidation of naphthalene to cis-1,2-dihydroxy-1,2-dihydronaphthalene in a membrane bioreactor
10.1002/(sici)1097-4660(199608)66:4<375::aid-jctb509>3.0.co;2-a
Reactivity of glucosyl radical in the presence of phenols
10.1016/0040-4020(96)00558-3
ALKYLATION OF CHIRAL PHOSPHONOGLYCINE EQUIVALENTS - ASYMMETRIC-SYNTHESIS OF DIETHYL ALPHA-AMINO-ALPHA-ALKYL-PHOSPHONATES
10.1016/0040-4020(94)01059-9
ESTIMATE OF DONOR AND ACCEPTOR SITES USING ALTERNATING POLARITY PRINCIPLE - APPLICATION TO PYRIDINE RING CONSTRUCTION
10.1021/ci00028a017
LILITH - FROM CHILDHOOD TO ADOLESCENCE
10.1021/ci00017a015
SIMILAR GROUP INTERFERENCES - A GENERAL-APPROACH TO THE LOCATION OF INTERFERING FUNCTIONALITIES
10.1016/s0040-4020(01)90164-4
A NEW DEFINITION OF FUNCTIONAL-GROUPS AND A GENERAL PROCEDURE FOR THEIR IDENTIFICATION IN ORGANIC STRUCTURES
10.1021/ja00035a023
ASYMMETRIC-SYNTHESIS OF DIETHYL ALPHA-AMINO-ALPHA-ALKYL-PHOSPHONATES BY ALKYLATION OF CHIRAL PHOSPHONOGLYCINE EQUIVALENTS - ROLE OF CHELATING EFFECTS
10.1016/s0957-4166(00)82094-7
NEW METHOD FOR THE CALCULATION OF BOND NATIVE POLARITY USING MOLECULAR ELECTRONIC-ENERGY
10.1021/ci00006a001
REACTION PREDICTION - THE SUGGESTIONS OF THE BEPPE PROGRAM
10.1021/ci00010a019
STUDIES TOWARD A MODEL FOR PREDICTING THE DIASTEREOSELECTIVITY IN THE ELECTROPHILIC AMINATION OF CHIRAL 1,3,2-OXAZAPHOSPHOLANES
10.1016/s0040-4020(01)88266-1
COMPUTER-ASSISTED ORGANIC-SYNTHESIS PLANNING - EFFECTIVE BOND POLARITY AS A GUIDELINE TO REACTIVITY
10.1021/ja00007a024
A NEW METHOD FOR THE CALCULATION OF ATOMIC AND LOCAL HARDNESS
10.1002/jcc.540110604
CYCLOARTANE TRITERPENE GLYCOSIDES FROM EGYPTIAN ASTRAGALUS SPECIES
10.1016/0031-9422(90)80198-p
GEOMETRIC REQUIREMENTS FOR REACTIVITY - THE SIMULATION OF ACCESS TO REACTION CENTERS AND THE INFLUENCE OF ATOMIC DEFORMATION ON IT
10.1021/ci00068a017
THE LILITH APPROACH TO ORGANIC-SYNTHESIS PLANNING
10.1016/s0003-2670(00)82076-0
ORGANIC-SYNTHESIS PLANNING - AN ALGORITHM FOR SELECTING STRATEGIC BOND FORMING SEQUENCES
10.1016/s0040-4020(01)80096-x
DETERMINATION OF ERGOTHIONEINE IN RED BLOOD-CELLS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
10.1016/0378-4347(88)80074-4
ORGANIC-SYNTHESIS PLANNING - A NEW ALGORITHM FOR STRATEGIC BOND PERCEPTION
10.1016/s0040-4020(01)85899-3
Synthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents
10.1039/C8MD00147B
Identification of viable TCDD access pathways to human AhR PAS-B ligand binding domain
10.1016/j.jmgm.2021.107886
Erika Corretto
Corretto Erika
ORCID: 0000-0002-7767-5191
Metagenomics of plant microbiomes
10.1007/978-3-319-61510-3_11
The draft genome sequence of Paenibacillus polymyxa strain CCI-25 encompasses high potential for secondary metabolite production
10.1128/genomeA.00366-16
Complete genome sequence of the heavy metal resistant bacterium Agromyces aureus AR33T and comparison with related Actinobacteria
10.1186/s40793-016-0217-z
Root-associated bacteria promote grapevine growth: from the laboratory to the field
10.1007/s11104-016-3019-6
Multienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid
10.1016/j.tetasy.2010.07.007
Qualitative analysis of biosurfactants from Bacillus species exhibiting antifungal activity
10.1371/journal.pone.0198107
Draft genome sequences of 10 Microbacterium spp., with emphasis on heavy metalcontaminated environments
10.1128/genomeA.00432-15
Agromyces aureus sp. nov., isolated from the rhizosphere of Salix caprea L. grown in a heavy-metal-contaminated soil
10.1099/ijsem.0.001260
Combined amendment of immobilizers and the plant growth-promoting strain Burkholderia phytofirmans PsJN favours plant growth and reduces heavy metal uptake
10.1016/j.soilbio.2015.08.038
Correction: Qualitative analysis of biosurfactants from Bacillus species exhibiting antifungal activity(PLoS ONE (2018) 13:6 (e0198107) DOI: 10.1371/journal.pone.0198107)
10.1371/journal.pone.0201624
Comparative Genomics of Microbacterium Species to Reveal Diversity, Potential for Secondary Metabolites and Heavy Metal Resistance.
10.3389/fmicb.2020.01869
A Human Lung-Associated Streptomyces sp. TR1341 Produces Various Secondary Metabolites Responsible for Virulence, Cytotoxicity and Modulation of Immune Response.
10.3389/fmicb.2019.03028
Comparative genome sequencing reveals insights into the dynamics of Wolbachia in native and invasive cherry fruit flies
10.1111/mec.15923
The Genome Analysis of the Human Lung-Associated Streptomyces sp. TR1341 Revealed the Presence of Beneficial Genes for Opportunistic Colonization of Human Tissues
10.3390/microorganisms9081547
Fulvia Orsini
Orsini Fulvia
ORCID: 0000-0003-4165-1398
Synthesis and antinociceptive activity of chimonanthines and pyrrolidinoindoline-type alkaloids
10.1016/S0968-0896(02)00078-0
Insect pest control agents: Novel chiral butanoate esters (juvenogens)
10.1016/j.bmc.2007.06.043
Multienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid
10.1016/j.tetasy.2010.07.007
Conformational analysis of cis- and (trans-1,2-dihydro-1,2-dihydroxynaphthalene
10.1016/0166-1280(92)85098-6
Synthesis of biologically active polyphenolic glycosides (combretastatin and resveratrol series)
10.1016/S0008-6215(97)00087-6
Zinc (0) Mediated Regio and Stereoselective Coupling of Substituted Bromocrotonates
10.1080/00397918408062820
Pyranocoumarins as potential photochemotherapeutic agents: theoretical and physico-chemical studies on the mechanism of action
10.1016/0223-5234(91)90130-F
Application of molecular modelling to natural products: a biogenetic study of (+)-spathulenol and (+)-allospathulenol
10.1016/0166-1280(93)87181-C
Heavy metals in seawater in front of a chlor-alkali plant
10.1016/0025-326X(87)90626-6
Oxygen‐17 NMR chemical shifts of esters
10.1002/mrc.1270221011
Alkaloid and lignan constituents of Cinnamosma madagascariensis
10.1016/0031-9422(79)83067-8
Selective enzymatic reduction of aldehydes
10.3390/11050365
Behaviour of aminoacids and aliphatic aldehydes in dipolar aprotic solvents: Formation of oxazolidinones—behaviour of aminoacids and aliphatic aldehydes in dipolar aprotic solvents
10.1002/jhet.5570260360
A reformatsky reagent. C-C bonds formation by substitution reactions
10.1080/00397918308081832
An ab initio and semiempirical approach to the reaction of zinc hydride with formaldehyde
10.1016/0166-1280(88)80451-2
A convenient procedure for the preparation of t-butyldimethylsilyl ethers of hydroxyamino acids
10.1080/00304948909356418
A new entry to β-hydroxyphosphonates: The SmI2-mediated reaction of diethyl iodomethylphosphonate with carbonyl compounds
10.1016/S0040-4039(02)01539-3
The unusual reactivity of 9-oxa-4-thia-tetracyclo[5.5.1.02,7.010,13] tridecan-12-one-3-spiro-1 '-cyclopentan-3'-ones: a molecular modelling study
10.1016/0166-1280(94)80067-7
Resveratrol Derivatives and Their Role as Potassium Channels Modulators
10.1021/np0303153
Application of (2R,3R)-dihydroxy-1,2,3,4-tetrahydronaphthalene to asymmetric synthesis
10.1016/S0957-4166(97)00088-8
Synthesis and biological evaluation of combretastatin analogs as cell cycle inhibitors of the G1 to S transition in Saccharomyces cerevisiae
10.1016/j.bmcl.2010.03.066
Synthesis and cardiotonic activity of novel pyrimidine derivatives: Crystallographic and quantum chemical studies
10.1021/jm9508649
Pd(O)-mediated cross-coupling of reformatsky reagents with vinyl- and aryl triflates
10.1080/00397918708057763
Oxygen-17 NMR spectroscopy: Effect of substituents on chemical shifts and width line in ortho substituted nitro benzenes
10.1080/00387018608069258
Conformational analysis and inotropic activity of 2-substituted-5-cyano-1,6-dihydro-6-oxo-3-pyridine carboxylates. II
10.1016/0223-5234(93)90095-V
Aminophosphonic acids and derivatives. Synthesis and biological applications
10.2174/092986710790149729
Structure and absolute stereochemistry of vanillosmin, a guaianolide from Vanillosmopsis erythropappa
10.1016/S0031-9422(00)91233-0
(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: A new chiral auxiliary for asymmetric Reformatsky reactions
10.1016/j.tetasy.2005.04.008
Natural stilbenes and analogues as antineoplastic agents
10.1016/S1572-5995(08)80025-7
Isolation, synthesis, and antiplatelet aggregation activity of resveratrol 3-O-β-D-glucopyranoside and related compounds
10.1021/np970069t
The structure of annonalide
10.1016/S0040-4039(01)92837-0
Saponins from Albizzia lucida
10.1016/0031-9422(91)83477-3
Separation of natural polar substances by reversed-phase high-performance liquid chromatography, centrifugal thin-layer chromatography and droplet counter-current chromatography
10.1016/S0021-9673(00)90634-4
A preparation of the ethylene glycol mono-ketal of cyclohexane-1,4-dione
10.1080/00397917508064122
Alcohol and 1,2-diol dehydrogenases: Synthetic use as oxidants
10.2174/157019306775474167
3,3′-Di [1,3-thiazolidine-4-one] system. VI. Structural and conformational studies on configurational isomers with antihistaminic activity
10.1016/0223-5234(94)90102-3
Reformatsky intermediate. A C-metallated species.
10.1016/S0040-4039(00)87750-3
Diels-Alder cycloadditions of 1,4-diaza-1,3-butadienes: A MNDO investigation
10.1016/S0040-4020(01)89529-6
Chemoenzymatic synthesis of conduritol analogues
10.1016/j.tetlet.2004.10.072
Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis
10.1016/j.tetasy.2006.01.009
Cardiotonic agents: a crystallographic and quantum-chemical study of ethyl 5-cyano-1,6-dihydro-2-isopropyl-6-oxo-3-pyridine carboxylate and related compounds
10.1016/0223-5234(90)90006-O
Organometallic Compounds of Zinc as Selective Nucleophilic Reagents in Organic Synthesis
10.1080/00397918408075723
Saponins from Albizzia anthelmintica
10.1016/0031-9422(89)80131-1
Cyclic chiral diols with C2 symmetry: Synthesis of (2R, 3R)-dihydroxy-1,2,3,4-tetrahydronaphthalene
10.1016/0957-4166(96)00108-5
New stereoselective synthesis of phosphono analogues of glycosyl phosphates
10.1016/S0957-4166(02)00329-4
Reformatsky reactions with SmI2 in catalytic amount
10.1016/j.tetlet.2005.01.079
Cobalt(0)-mediated addition of α-haloesters and α-haloketones to (R)-2,3-O-cyclohexylideneglyceraldehyde
10.1016/S0957-4166(97)00521-1
1,3‐Dipolar cycloadditions of azomethine ylides with dipolarophiles. II. Synthesis of pyrrolizidines
10.1002/jhet.5570250612
Polyphenolic glycosides from african proteaceae
10.1021/np9902237
Organic phase effect in the biphasic bioconversion of substituted naphthalenes by engineered E. coli containing P. fluorescens N3 dioxygenase
10.1016/j.molcatb.2003.10.013
Enantiopure vic-amino alcohols and vic-diamines from (1R,2S)-1,2-dihydroxy-1,2-dihydronaphthalene
10.1016/S0957-4166(01)00510-9
Oxygen-17 NMR spectroscopy: Effect of substituents on chemical shifts for o- m- p- substituted benzoic acids, phenylacetic and methyl benzoates
10.1080/00387018608069223
Dioxygenation of naphthalene by Pseudomonas fluorescens N3 dioxygenase: Optimization of the process parameters
10.1002/bit.20736
Biotransformation of styrenes by a Pseudomonas putida
10.1007/BF00256214
Cycloartane triterpene glycosides from Astragalus alexandrinus
10.1016/S0031-9422(00)90598-3
A novel AMPK activator reduces glucose uptake and inhibits tumor progression in a mouse xenograft model of colorectal cancer
10.1007/s10637-014-0148-8
One-pot Wittig reactions in water and in the presence of a surfactant
10.1055/s-2006-947323
Conformational analysis and X-ray structure of 1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid
10.1007/BF01185548
A chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralins
10.1016/S0957-4166(02)00098-8
Influence of the catalyst on the Pd0-mediated reactions of BrZnCH(CH3 ) COOtBu with vinyl and aryl triflates
10.1016/0022-328X(89)87059-7
SmI2-mediated reactions of diethyl iodomethylphosphonate with esters and lactones: A highly stereoselective synthesis of a precursor of the C-glycosyl analogue of thymidine 5′-(β-L-rhamnosyl)diphosphate
10.1016/S0040-4039(02)01540-X
Bioconversion of substituted naphthalenes to the corresponding 1,2-dihydro derivatives by Escherichia coli recombinant strains
10.1016/S0040-4039(97)01404-4
Cycloartane triterpene glycosides from EgyptianAstragalus species
10.1016/0031-9422(90)80198-P
Zinc (0)-Mediated Formation Of Carbon-Carbon Bond From Y-Bromo Crotonate.
10.1080/00397918208065982
Synthesis of Resveratrol Derivatives and in Vitro Screening for Potential Cancer Chemopreventive Activities
10.1002/ardp.201600022
Synthesis of C-glycosyl compounds: the reaction of acetylated glycals with tert-butoxycarbonylmethylzinc bromide
10.1016/0008-6215(93)84090-S
A cycloartane triterpene 3β, 16β diglucoside from Astragalus trigonus and its non natural 6-hydroxy epimer
10.1016/S0031-9422(97)00869-8
Multienzymatic preparation of (-)-[3-(oxiran-2-yl)phenyl]methanol and (-)-3-(oxiran-2-yl)benzoic acid
10.1016/j.tetasy.2009.03.023
Structural and conformational studies on 3,3'-bis [1,3-thiazolidin-4-one] derivatives with biological activity
10.1016/S0022-2860(97)00375-X
The C-13 configuration of annonalide
10.1016/S0040-4039(01)87353-6
Quadranguloside, a cycloartane triterpene glycoside from Passiflora quadrangularis
10.1016/S0031-9422(00)94527-8
13C NMR spectra of cassane diterpenoids. The stereochemistry of the caesalpins
10.1002/mrc.1270170303
Triterpene glycosides related to quadranguloside from Passiflora quadrangularis
10.1016/S0031-9422(00)82358-4
Study of the resolution of amino acids and aminoalcohols in organic solvents
10.1007/BF00805834
C-Metallated reformatsky intermediates. Structure and reactivity.
10.1016/S0040-4020(01)96898-X
Recent developments in epoxide preparation
10.2174/157017906778699503
Alcohol and 1,2-diol dehydrogenases: Synthetic use in the preparation of chiral alcohols by carbonyl reduction
10.2174/157019306775474185
Bacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: Study of the effects of substituent nature and position
10.1016/j.tetasy.2004.04.005
Triterpenes in leaves of Olea europaea
10.1016/0031-9422(75)85210-1
3,3′-di[1,3-thiazolidin-4-one] system. Structural and conformational studies on configurational isomers with anti-inflammatory activity
10.1007/BF01667029
Development of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions
10.1016/S0923-2508(00)00161-3
Low-valent complexes of cobalt and phosphorus donor ligands as mediators in Reformatsky-type reactions
10.1016/0022-328X(95)05468-5
A stereoconvergent approach to dicyclopenta[a,d]cyclooctane terpenoids via a very mild cope reaction
10.1016/0040-4039(91)80457-H
Biocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactions
10.1016/j.molcatb.2007.10.014
1,2-Dihydro-1,2-dihydroxynaphthalene dehydrogenase containing recombinant strains: Preparation, isolation and characterisation of 1,2- dihydroxynaphthalenes and 1,2-naphthoquinones
10.1016/S0040-4020(99)00135-0
1,3 Dipolar cycloadditions of azomethine ylides with aromatic aldehydes. syntheses of 1-oxapyrrolizidines and 1,3-oxazolidines.
10.1016/S0040-4020(01)85842-7
A new Co(0) complex mediated synthesis of C-glycoside analogues
10.1016/S0957-4166(03)00533-0
Reformatsky-type co-mediated synthesis of β-hydroxyphosphonates
10.1016/S0040-4039(97)10819-X
Synthesis and biological evaluation of 1,4-diaryl-2-azetidinones as specific anticancer agents: Activation of adenosine monophosphate activated protein kinase and induction of apoptosis
10.1021/jm201344a
One-pot, fluoride-promoted wittig reaction
10.1080/00397910802654633
Alkaloids of Hazunta modesta
10.1016/S0031-9422(00)94259-6
Use of oxidoreductive enzymes in sequential biotransformations
10.1016/j.nbt.2009.06.394
Isolation, cloning and synthetic use of the tHBP aldolase from Pseudomonas fluorescens N3
10.1016/j.jbiotec.2007.07.177
Preparation and synthetic use of enantiopure naphthalene dihydrodiols
10.2174/1570193043488944
Transition metals-mediated Reformatsky reactions
10.2174/1570179043485385