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Asymmetric synthesis of both enantiomers of tomoxetine and fluoxetine. Selective reduction of 2,3-epoxycinnamyl alcohol with Red-Al
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Asymmetric Epoxidation of Allylic Alcohols: the Katsuki–Sharpless Epoxidation Reaction
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Straightforward Access to Enantiomerically Pure, Highly Functionalized Pyrrolizidines by Cycloaddition of Maleic Acid Esters to Pyrroline N-Oxides Derived from Tartaric, Malic and Aspartic Acids − Synthesis of (−)-Hastanecine, 7-epi-Croalbinecine and (−)-Croalbinecine
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Sodium bis(2‐methoxyethoxy)aluminum hydride ( SMEAH , Red‐ Al Ò)
inferred← citeshttps://doi.org/10.1002/9780471264194.fos09016.pub2openalex-snapshot
Sodium bis(2‐methoxyethoxy)aluminum hydride ( SMEAH , Red‐ Al Ò)
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Transition‐Metal–Catalyzed Stereoselective Oxidations in Drug and Natural Product Synthesis
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Formation of Ethers by Alkylation of Alcohols, Phenols, and Derivatives
inferred← citeshttps://doi.org/10.1002/9781118662083.cot07-007openalex-snapshot
Formation of Alcohols and Phenols by Ether Cleavage
inferred← citeshttps://doi.org/10.1002/adsc.200390021openalex-snapshot
Enantioselective Hydrogenation of β‐Keto Esters using Chiral Diphosphine‐Ruthenium Complexes: Optimization for Academic and Industrial Purposes and Synthetic Applications
inferred← citeshttps://doi.org/10.1002/adsc.201100305openalex-snapshot
Ruthenium‐Catalyzed Asymmetric Hydrogenation of β‐Keto‐ enamines: An Efficient Approach to Chiral γ‐Amino Alcohols
inferred← citeshttps://doi.org/10.1002/adsc.201500653openalex-snapshot
Asymmetric Hydrogenation of β‐Secondary Amino Ketones Catalyzed by a Ruthenocenyl Phosphino‐oxazoline‐ruthenium Complex (RuPHOX‐Ru): the Synthesis of γ‐Secondary Amino Alcohols
inferred← citeshttps://doi.org/10.1002/adsc.202200524openalex-snapshot
Divergent Synthesis of β‐Hydroxy Amides (Esters) and γ‐Amino Alcohols via Ir/f‐Diaphos Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/ange.200352431openalex-snapshot
Efficient Synthesis of Chiral α‐ and β‐Hydroxy Amides: Application to the Synthesis of ( R )‐Fluoxetine
inferred← citeshttps://doi.org/10.1002/ange.200462178openalex-snapshot
Practical Synthesis of Enantiopure γ‐Amino Alcohols by Rhodium‐Catalyzed Asymmetric Hydrogenation of β‐Secondary‐Amino Ketones
inferred← citeshttps://doi.org/10.1002/ange.201411384openalex-snapshot
ZnCl 2 ‐Promoted Asymmetric Hydrogenation of β‐Secondary‐Amino Ketones Catalyzed by a P‐Chiral Rh–Bisphosphine Complex
inferred← citeshttps://doi.org/10.1002/ange.201500880openalex-snapshot
Remote Hydroxylation through Radical Translocation and Polar Crossover
inferred← citeshttps://doi.org/10.1002/ange.202009754openalex-snapshot
Anti‐Markovnikov Hydroamination of Racemic Allylic Alcohols to Access Chiral γ‐Amino Alcohols
inferred← citeshttps://doi.org/10.1002/anie.200352431openalex-snapshot
Efficient Synthesis of Chiral α‐ and β‐Hydroxy Amides: Application to the Synthesis of (R)‐Fluoxetine
inferred← citeshttps://doi.org/10.1002/anie.200462178openalex-snapshot
Practical Synthesis of Enantiopure γ‐Amino Alcohols by Rhodium‐Catalyzed Asymmetric Hydrogenation of β‐Secondary‐Amino Ketones
inferred← citeshttps://doi.org/10.1002/anie.201411384openalex-snapshot
ZnCl2‐Promoted Asymmetric Hydrogenation of β‐Secondary‐Amino Ketones Catalyzed by a P‐Chiral Rh–Bisphosphine Complex
inferred← citeshttps://doi.org/10.1002/anie.201500880openalex-snapshot
Remote Hydroxylation through Radical Translocation and Polar Crossover
inferred← citeshttps://doi.org/10.1002/anie.202009754openalex-snapshot
Anti‐Markovnikov Hydroamination of Racemic Allylic Alcohols to Access Chiral γ‐Amino Alcohols
inferred← citeshttps://doi.org/10.1002/aoc.70571openalex-snapshot
Highly Efficient Preparation of Chiral β ‐ or γ ‐Amino Alcohols and Pharmaceutical Intermediates by Ir/f‐Amphbinol‐Catalyzed Enantioselective Hydrogenation
inferred← citeshttps://doi.org/10.1002/cctc.202100738openalex-snapshot
Phase Separation‐Promoted Redox Deracemization of Secondary Alcohols over a Supported Dual Catalysts System
inferred← citeshttps://doi.org/10.1002/chem.201000804openalex-snapshot
The Cobalt Way to Angucyclinones: Asymmetric Total Synthesis of the Antibiotics (+)‐Rubiginone B2, (−)‐Tetrangomycin, and (−)‐8‐O‐Methyltetrangomycin
inferred← citeshttps://doi.org/10.1002/chem.201404215openalex-snapshot
Highly Enantioselective Cross‐Aldol Reactions of Acetaldehyde Mediated by a Dual Catalytic System Operating under Site Isolation
inferred← citeshttps://doi.org/10.1002/chin.198905144openalex-snapshot
ChemInform Abstract: Asymmetric Synthesis of Both Enantiomers of Tomoxetine and Fluoxetine. Selective Reduction of 2,3‐Epoxycinnamyl Alcohol with Red‐Al.
inferred← citeshttps://doi.org/10.1002/chir.20368openalex-snapshot
Application of chiral technology in a pharmaceutical company. Enantiomeric separation and spectroscopic studies of key asymmetric intermediates using a combination of techniques. Phenylglycidols
inferred← citeshttps://doi.org/10.1002/chir.20814openalex-snapshot
Modification of chiral dimethyl tartrate through transesterification: Immobilization on POSS and enantioselectivity reversal in sharpless asymmetric epoxidation
inferred← citeshttps://doi.org/10.1002/chir.23043openalex-snapshot
Chiral porphyrin imine manganese complex as catalyst for asymmetric epoxidation of styrene derivatives
inferred← citeshttps://doi.org/10.1002/chir.530040212openalex-snapshot
Effective methods for enantioselective analysis of glycidol derivatives by liquid chromatography
inferred← citeshttps://doi.org/10.1002/cjoc.19920100411openalex-snapshot
A microbially based approach for the asymmetric synthesis of both enantiomers of R‐ and S‐fluoxetine
inferred← citeshttps://doi.org/10.1002/cjoc.20030210802openalex-snapshot
Asymmetric Syntheses Aided by Biocatalysts
inferred← citeshttps://doi.org/10.1002/cplu.201800377openalex-snapshot
Yolk‐Shell‐Mesostructured Silica‐Supported Dual Molecular Catalyst for Enantioselective Tandem Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201300083openalex-snapshot
Towards the Synthesis of Lyngbyaloside B: Stereoselective Synthesis of the C1–C16 Macrolactone Core Segment
inferred← citeshttps://doi.org/10.1002/hlca.19940770323openalex-snapshot
Studies Directed toward the Synthesis of Phomenoic Acid. Part 1. Enantioselective synthesis of the C(1)‐to‐C(6) segment
inferred← citeshttps://doi.org/10.1002/hlca.200490139openalex-snapshot
Transition‐Metal‐Based Lewis Acid Catalysis of Aza‐Type Michael Additions of Amines to α,β‐Unsaturated Electrophiles in Water
inferred← citeshttps://doi.org/10.1002/jlcr.2580310608openalex-snapshot
An enantioselective synthesis of S‐γ‐[(4‐trifluoromethyl)phenoxy]benzenepropanamine‐[3‐14C] hydrochloride, an important metabolite of fluoxetine hydrochloride
inferred← citeshttps://doi.org/10.1002/jlcr.2580330805openalex-snapshot
Synthesis of [18F]‐(S)‐fluoxetine: A selective serotonine uptake inhibitor
inferred← citeshttps://doi.org/10.1002/jlcr.2580360303openalex-snapshot
An asymmetric synthesis of duloxetine hydrochloride, a mixed uptake inhibitor of serotonin and norepinephrine, and its C‐14 labeled isotopomers
inferred← citeshttps://doi.org/10.1002/slct.201802099openalex-snapshot
A Facile Preparation of Hydroxycinnamyl Alcohols withSimultaneous Protection of Phenol Groups as Carbonate
inferred← citeshttps://doi.org/10.1007/s10337-012-2289-2openalex-snapshot
Enantioseparation of Chiral Epoxides with Polysaccharide-Based Chiral Columns in HPLC
inferred← citeshttps://doi.org/10.1007/s10563-026-09479-4openalex-snapshot
Vanadium-Catalyzed Epoxidation of Alkenes
inferred← citeshttps://doi.org/10.1016/0040-4020(94)01096-iopenalex-snapshot
Total synthesis of phytosiderophores
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00059-hopenalex-snapshot
Synthesis of 2,6-dideoxy-4-S-methyl-4-thio-d-ribo-hexopyranose, a component of the esperamicin oligosaccharide
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00429-copenalex-snapshot
Studies of regio- and stereoselectivity in some nucleophilic ring opening reactions of N-tosyl-3-phenyl-2-aziridinemethanols and derivatives
inferred← citeshttps://doi.org/10.1016/0968-0896(96)00077-6openalex-snapshot
An efficient chemoenzymatic route to the antidepressants (R)-fluoxetine and (R)-tomoxetine
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00196-7openalex-snapshot
Addition Reactions with Formation of Carbon–Oxygen Bonds: (ii) Asymmetric Methods of Epoxidation
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00249-3openalex-snapshot
Reduction of Epoxides
inferred← citeshttps://doi.org/10.1016/b978-0-12-801457-8.00012-4openalex-snapshot
Use of Catalysis for API Manufacturing
inferred← citeshttps://doi.org/10.1016/b978-0-12-824092-2.00010-1openalex-snapshot
Transition metal-catalysed reactions: Diastereoselectivity and asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/b978-008096518-5.00003-4openalex-snapshot
Oxiranes and Oxirenes: Monocyclic
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.07.005openalex-snapshot
Perspectives and industrial potential of PGA selectivity and promiscuity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.06.005openalex-snapshot
Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives
inferred← citeshttps://doi.org/10.1016/j.jcat.2019.07.005openalex-snapshot
Integrated soluble polymer and mesoporous silica as a double–type support to immobilize tertiary amine–Ru/diamine–bifunctionality for aza–addition/reduction cascade reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.03.030openalex-snapshot
Ultrasound-irradiated Michael addition of amines to ferrocenylenones under solvent-free and catalyst-free conditions at room temperature
inferred← citeshttps://doi.org/10.1016/j.molcatb.2008.05.013openalex-snapshot
Microbial production of (S)-1-phenyl-1,3-propanediol by stereospecific reduction of 3-hydroxy-1-phenylpropane-1-one
inferred← citeshttps://doi.org/10.1016/j.tet.2006.10.006openalex-snapshot
5-Phenylthio-1,3-oxazinan-4-ones via hetero Diels–Alder reactions: synthesis of (R)- and (S)-Duloxetines and Fluoxetines
inferred← citeshttps://doi.org/10.1016/j.tet.2018.04.022openalex-snapshot
A site isolation-enabled organocatalytic approach to enantiopure γ-amino alcohol drugs
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.09.007openalex-snapshot
Enantio- and regiospecific reduction of ethyl 4-phenyl-2,4-dioxobutyrate with baker’s yeast: preparation of (R)-HPB ester
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.09.009openalex-snapshot
Synthesis of enantiomerically pure (S)- and (R)-fluoxetine (Prozac®) via a hetero Diels–Alder strategy
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.11.005openalex-snapshot
Asymmetric dihydroxylation route to (R)-isoprenaline, (R)-norfluoxetine and (R)-fluoxetine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.04.002openalex-snapshot
Polymer-supported chiral sulfonamide catalyzed one-pot reduction of β-keto nitriles: a practical synthesis of (R)-fluoxetine and (R)-duloxetine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.12.022openalex-snapshot
Preparation of enantiomerically pure (R)- and (S)-3-amino-3-phenyl-1-propanol via resolution with immobilized penicillin G acylase
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.10.046openalex-snapshot
Asymmetric transfer hydrogenation of 2-tosyloxy-1-(4-hydroxyphenyl)ethanone derivatives: synthesis of (R)-tembamide, (R)-aegeline, (R)-octopamine, and (R)-denopamine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.11.002openalex-snapshot
Enantioselective Rh-catalyzed transfer hydrogenation of α-sulfonyloxy heteroaryl ketones; asymmetric synthesis of (S)-bufuralol
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.04.034openalex-snapshot
Direct catalytic asymmetric aldol reaction of thioamides: a concise asymmetric synthesis of (R)-fluoxetine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.06.003openalex-snapshot
Chemoenzymatic asymmetric synthesis of fluoxetine, atomoxetine, nisoxetine, and duloxetine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.11.052openalex-snapshot
Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidine derived from (1S,2S,3R,4R)-3-amino-7,7-dimethoxynorbornan-2-ol. An efficient synthesis of enantiopure (R)-tomoxetine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.05.070openalex-snapshot
Asymmetric synthesis of (+)-passifloricin A and its 6-epimer
inferred← citeshttps://doi.org/10.1016/s0022-328x(98)01048-1openalex-snapshot
The palladium-catalysed arylation and vinylation of alkenes—enantioselective fashion
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)01012-2openalex-snapshot
Enantioselective synthesis of (S)- and (R)-fluoxetine hydrochloride
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)88039-xopenalex-snapshot
Total synthesis of mugineic acid. Efficient use of the phenyl group as the carboxyl synthon
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89866-5openalex-snapshot
Asymmetric synthesis of both enantiomers of fluoxetine via microbiological reduction of ethyl benzoylacetate
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00325-6openalex-snapshot
Stereoselective synthesis of 2-aryloxy esters: An asymmetric approach to fluoxetine, tomoxetine and nisoxetine
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00437-7openalex-snapshot
The asymmetric Heck reaction
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61791-4openalex-snapshot
The palladium-catalyzed arylation of 4H-1,3-dioxin
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74778-2openalex-snapshot
Efficient synthesis of mugineic acid, a typical phytosiderophore, utilizing the phenyl group as the carboxyl synthon
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)76212-5openalex-snapshot
A convenient method for preparing enantiomerically pure norfluoxetine, fluoxetine and tomoxetine
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85993-6openalex-snapshot
A new chemoenzymatic enantioselective synthesis of R-(−)-tomoxetine, (R)- and (S)-fluoxetine.
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)97251-4openalex-snapshot
Asymmetric synthesis and absolute stereochemistry of LY248686
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01877-9openalex-snapshot
A practical asymmetric synthesis of (R)-fluoxetine and its major metabolite (R)-norfluoxetine
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)93743-8openalex-snapshot
Enantioselective and practical syntheses of R- and S-fluoxetines
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00842-0openalex-snapshot
An asymmetric dihydroxylation route to enantiomerically pure norfluoxetine and fluoxetine
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01073-0openalex-snapshot
Pd-Catalyzed kinetic resolution of benzylic alcohols: a practical synthesis of (R)-tomoxetine and (S)-fluoxetine hydrochlorides
inferred← citeshttps://doi.org/10.1016/s0040-4039(96)02136-3openalex-snapshot
Highly efficient enzymatic resolution of homoallyl alcohols leading to a simple synthesis of optically pure fluoxetine and related compounds
inferred← citeshttps://doi.org/10.1016/s0731-7085(02)00605-2openalex-snapshot
Utilizing capillary gas chromatography mass spectrometry to determine 4-benzotrifluoride t-butyl ether as a reaction by-product in fluoxetine synthesized using potassium t-butoxide as base
inferred← citeshttps://doi.org/10.1016/s0957-4166(00)80257-8openalex-snapshot
An efficient route to enantiomerically pure antidepressants: tomoxetine, nisoxetine and fluoxetine
inferred← citeshttps://doi.org/10.1016/s0957-4166(00)80431-0openalex-snapshot
Stereochemical features of baker's yeast mediated transformation of racemic and enantiomerically pure 2-deutero-3-chloropropiophenone
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00537-2openalex-snapshot
Chemoenzymatic synthesis2 of both enantiomers of fluoxetine, tomoxetine and nisoxetine: lipase-catalyzed resolution of 3-aryl-3-hydroxypropanenitriles
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00074-9openalex-snapshot
Synthesis of novel C2-symmetric ligands based on (R,R)- and (S,S)-diphenyl-1,3-propanediol
inferred← citeshttps://doi.org/10.1021/acs.oprd.0c00193openalex-snapshot
Convenient Continuous Flow Synthesis of N-Methyl Secondary Amines from Alkyl Mesylates and Epoxides
inferred← citeshttps://doi.org/10.1021/acs.oprd.5b00209openalex-snapshot
Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat
inferred← citeshttps://doi.org/10.1021/acs.organomet.2c00327openalex-snapshot
Theoretical Exploration of Mechanism and Ligand Effects of Asymmetric Hydrogenation of β-Amino Ketone Catalyzed by an Iridium-PNN Catalyst
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02614openalex-snapshot
Asymmetric Synthesis of γ-Secondary Amino Alcohols via a Borrowing-Hydrogen Cascade
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02309openalex-snapshot
Electrochemical Oxidation Enables Regioselective 1,3-Hydroxyfunctionalization of Cyclopropanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01106openalex-snapshot
Pd/WingPhos-Catalyzed Synthesis of γ-Amino Alcohol Derivatives with β-Axial Stereogenicity via Desymmetrization of Allenylic Cyclic Carbonates
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01989openalex-snapshot
Photochemical C–O Coupling of Chiral Alcohols with Aryl Halides by Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00823openalex-snapshot
A Michael Addition–Asymmetric Transfer Hydrogenation One-Pot Enantioselective Tandem Process for Syntheses of Chiral γ-Secondary Amino Alcohols
inferred← citeshttps://doi.org/10.1021/acscatal.1c01199openalex-snapshot
Manganese-Catalyzed Anti-Markovnikov Hydroamination of Allyl Alcohols via Hydrogen-Borrowing Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.5c00312openalex-snapshot
Engineering Limonene Epoxide Hydrolases for the Enantiocomplementary Synthesis of Chiral 1,3-Diols and Oxetanes
inferred← citeshttps://doi.org/10.1021/cn400186jopenalex-snapshot
Classics in Chemical Neuroscience: Fluoxetine (Prozac)
inferred← citeshttps://doi.org/10.1021/cr030700xopenalex-snapshot
Enantioselective Palladium-Catalyzed Transformations
inferred← citeshttps://doi.org/10.1021/cr040700copenalex-snapshot
Asymmetric Synthesis of Active Pharmaceutical Ingredients
inferred← citeshttps://doi.org/10.1021/jacs.1c10245openalex-snapshot
The Catalytic Asymmetric Intermolecular Prins Reaction
inferred← citeshttps://doi.org/10.1021/jo0101860openalex-snapshot
Highly Diastereoselective 1,4-Addition of an Organocuprate to Methyl α- d -Gluco-, α- d -Manno-, or α- d -Galactopyranosides Tethering an α,β-Unsaturated Ester. Novel Asymmetric Access to β-C-Substituted Butanoic Acids
inferred← citeshttps://doi.org/10.1021/jo051207jopenalex-snapshot
(S,S)-(+)-Pseudoephedrine as Chiral Auxiliary in Asymmetric Aza-Michael Reactions. Unexpected Selectivity Change when Manipulating the Structure of the Auxiliary
inferred← citeshttps://doi.org/10.1021/jo300002uopenalex-snapshot
Syntheses of Chiral β- and γ-Amino Ethers, Morpholines, and Their Homologues via Nucleophilic Ring-Opening of Chiral Activated Aziridines and Azetidines
inferred← citeshttps://doi.org/10.1021/jo801568aopenalex-snapshot
Regio- and Stereoselective Ring Opening of Enantiomerically Enriched 2-Aryl Oxetanes and 2-Aryl Azetidines with Aryl Borates
inferred← citeshttps://doi.org/10.1021/jo951403yopenalex-snapshot
Synthesis of trans-3,4-Dimethyl-4-(3-hydroxyphenyl)piperidine Opioid Antagonists: Application of the Cis-Thermal Elimination of Carbonates to Alkaloid Synthesis
inferred← citeshttps://doi.org/10.1021/ol0160250openalex-snapshot
Studies on the Synthesis of Pectenotoxin II: Synthesis of a C(11)−C(26) Fragment Precursor via [3 + 2]-Annulation Reactions of Chiral Allylsilanes
inferred← citeshttps://doi.org/10.1021/ol047691eopenalex-snapshot
Double Addition of Grignard Reagents to N-Glycosyl Nitrones: A New Tool for the Construction of Enantiopure Azaheterocycles
inferred← citeshttps://doi.org/10.1021/ol300949sopenalex-snapshot
Reversal of Selectivity in Acetate Aldol Reactions of N-Acetyl-(S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one
inferred← citeshttps://doi.org/10.1021/op400279nopenalex-snapshot
Controlling the Exothermicity of O-Arylation by Evaporative Cooling during the Process Development of Fluoxetine Hydrochloride
inferred← citeshttps://doi.org/10.1038/s42004-022-00678-4openalex-snapshot
Iridium-catalyzed enantioselective synthesis of chiral γ-amino alcohols and intermediates of (S)-duloxetine, (R)-fluoxetine, and (R)-atomoxetine
inferred← citeshttps://doi.org/10.1039/b000846jopenalex-snapshot
Chemoenzymatic synthesis of the non-tricyclic antidepressants Fluoxetine, Tomoxetine and Nisoxetine
inferred← citeshttps://doi.org/10.1039/c1cy00068copenalex-snapshot
Metal–organic frameworks as heterogeneous catalysts for oxidation reactions
inferred← citeshttps://doi.org/10.1039/c39940001903openalex-snapshot
Enantioconvergent preparation of the a-ring precursors of calcitriol from either (R)- or (S)-epichlorohydrin
inferred← citeshttps://doi.org/10.1039/c3gc37054bopenalex-snapshot
Aza-Michael versus aminolysis reactions of glycerol carbonate acrylate
inferred← citeshttps://doi.org/10.1039/c3ob40135aopenalex-snapshot
Asymmetric hydrogenation of β-amino ketones with the bimetallic complex RuPHOX-Ru as the chiral catalyst
inferred← citeshttps://doi.org/10.1039/c4ob01142bopenalex-snapshot
Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach
inferred← citeshttps://doi.org/10.1039/c5ob00809copenalex-snapshot
Synthesis, structure and reactivity of [15]-macrodilactones
inferred← citeshttps://doi.org/10.1039/c6ob00871bopenalex-snapshot
One-pot sequential asymmetric hydrogenation of β-aryl-β-aryloxy acroleins
inferred← citeshttps://doi.org/10.1039/d3cc03919fopenalex-snapshot
Iron-catalyzed β-hydroxymethylative carbonylation of styrene under photo-irradiation
inferred← citeshttps://doi.org/10.1039/d4ra07386jopenalex-snapshot
Ir-catalyzed reductive amination and transfer hydrogenation of diketones: access to β- and γ-amino alcohols
inferred← citeshttps://doi.org/10.1080/00397910008087074openalex-snapshot
Asymmetric Synthesis of Heptacosane-6,8-Diols Induced by Chiral Sulfoxides
inferred← citeshttps://doi.org/10.1080/00397911.2011.575522openalex-snapshot
Simple and Efficient Synthesis of ( S )-Dapoxetine
inferred← citeshttps://doi.org/10.1080/00397911.2024.2414410openalex-snapshot
Cobalt(II) catalyzed Michael-type hydroamination of activated olefins
inferred← citeshttps://doi.org/10.1080/00397919508012686openalex-snapshot
Synthesis of R- and S- Fluoxetine, Norfluoxetine and Related Compounds from Styrene Oxide
inferred← citeshttps://doi.org/10.1080/10242422.2020.1786070openalex-snapshot
Optimisation of the bioreduction process of carbonyl compounds promoted by seeds of glossy privet (Ligustrum lucidum - Oleaceae) and its application to the synthesis of key intermediates
inferred← citeshttps://doi.org/10.1080/10242422.2021.1956910openalex-snapshot
Whole seeds of Bauhinia variegata L. (Fabaceae) as an efficient biocatalyst for benzyl alcohol preparations from benzaldehydes
inferred← citeshttps://doi.org/10.1142/s1088424616500620openalex-snapshot
Asymmetric epoxidation of alkenes catalyzed by novel chiral porphyrin metal complexes
inferred← citeshttps://doi.org/10.1246/cl.1991.1603openalex-snapshot
Chemoenzymatic Synthesis of Both Enantiomers of Fluoxetine
inferred← citeshttps://doi.org/10.1246/cl.1994.2143openalex-snapshot
Synthesis of the Tetrahydrofuran Ring Part of a Marine Toxin Polycavernoside-A
inferred← citeshttps://doi.org/10.2174/2213335601666140610201546openalex-snapshot
aza-Michael Addition of Primary Amines by Lipases and Microwave Irradiation: A Green Protocol for the Synthesis of Propanenitrile Derivatives
inferred← citeshttps://doi.org/10.3389/fchem.2018.00272openalex-snapshot
Boron Tetrafluoride Anion Bonding Dual Active Species Within a Large–Pore Mesoporous Silica for Two–Step Successive Organic Transformaion to Prepare Optically Pure Amino Alcohols
inferred← citeshttps://doi.org/10.34248/bsengineering.1458736openalex-snapshot
Fluoksetin ve Norfluoksetinin Sentezi Üzerine Çalışmalar ve Antioksidant Özelliğinin Araştırılması
inferred← citeshttps://doi.org/10.5012/bkcs.2009.30.6.1317openalex-snapshot
Highly Enantioselective Rh-catalyzed Transfer Hydrogenation of α-Functionalized Arylketones
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