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Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric induction
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inferred← citeshttps://doi.org/10.1007/s13738-023-02858-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0040-4020(92)85018-aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0040-4039(91)80824-popenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0040-4039(94)02194-gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0957-4166(96)00150-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0957-4166(96)00230-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00098-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-08-092493-9.50014-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2006.03.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2014.10.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.11.035openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cclet.2021.05.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.crci.2007.12.004openalex-snapshot
Iron salts catalyzed synthesis of β-N-substituted aminoacrylates
inferred← citeshttps://doi.org/10.1016/j.crci.2011.09.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.crci.2011.11.012openalex-snapshot
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Functionalized carbon dot adorned coconut shell char derived green catalysts for the rapid synthesis of amidoalkyl naphthols
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2007.03.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jscs.2015.10.007openalex-snapshot
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Ordered organo-inorganic hybrid mesoporous solid acid catalysts (Zr–TMS–TFA) for Michael addition of indoles with α,β-unsaturated carbonyl compounds under environmentally benign solvent free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.06.061openalex-snapshot
A recyclable protocol for aza-Michael addition of amines to α,β-unsaturated compounds using Cu-Al hydrotalcite
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.11.025openalex-snapshot
ZrOCl2·8H2O as a highly efficient and the moisture tolerant Lewis acid catalyst for Michael addition of amines and indoles to α, β-unsaturated ketones under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.11.045openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcata.2014.06.031openalex-snapshot
Room temperature solvent free aza-Michael reactions over nano-cage mesoporous materials
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Lipase-catalyzed resolution of 1-chloro-3-[(4-morpholin-4-yl-1,2,5-thiadiazole-3-yl)oxy]propan-2-ol
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Lipase mediated resolution of γ-azidoalcohols in aqueous and organic media: Synthesis of (R)- and (S)-fluoxetine and duloxetine
inferred← citeshttps://doi.org/10.1016/j.molliq.2018.01.083openalex-snapshot
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Vibrational assignment and crystal structure of 3-amino-1-phenyl-2-buten-1-one
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.05.010openalex-snapshot
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Structure-activity relationship of the ionic cocrystal: 5-amino-2-naphthalene sulfonate·ammonium ions for pharmaceutical applications
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.044openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.097openalex-snapshot
Total synthesis of (+)-negamycin and its 5-epi-derivative
inferred← citeshttps://doi.org/10.1016/j.tet.2010.03.113openalex-snapshot
Diastereoselective synthesis of 6-functionalized 4-aryl-1,3-oxazinan-2-ones and their application in the synthesis of 3-aryl-1,3-aminoalcohols and 6-arylpiperidine-2,4-diones
inferred← citeshttps://doi.org/10.1016/j.tet.2010.10.067openalex-snapshot
Asymmetric syntheses of (+)-negamycin, (+)-3-epi-negamycin and sperabillin C via lithium amide conjugate addition
inferred← citeshttps://doi.org/10.1016/j.tet.2010.10.075openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2011.08.077openalex-snapshot
Synthesis of enantiopure β-amino alcohols via AKR/ARO of epoxides using recyclable macrocyclic Cr(III) salen complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.055openalex-snapshot
Henry–Nef reaction: a practical and versatile chiral pool route to 2-substituted pyrrolidine and piperidine alkaloids
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134289openalex-snapshot
Regioselective synthesis of functionalized cyclopent-2-enone-derived carbonylureas and enaminohydroxybarbiturates from alloxans in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.07.027openalex-snapshot
An efficient synthesis of enantiopure (+)- and (−)-syn-1,3-amino alcohols with a norbornane framework and their application in the asymmetric addition of ZnEt2 to benzaldehyde
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.02.015openalex-snapshot
New chemoenzymatic pathway for β-adrenergic blocking agents
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.04.009openalex-snapshot
Stereoselective synthesis of enantiopure γ-aminoalcohols by reduction of chiral β-enaminoketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.04.019openalex-snapshot
Lipase-mediated resolution of 3-hydroxy-4-trityloxybutanenitrile: synthesis of 2-amino alcohols, oxazolidinones and GABOB
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.03.028openalex-snapshot
Synthesis of enantiomerically pure γ-azidoalcohols by lipase-catalyzed transesterification
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.124openalex-snapshot
β-Cyclodextrin promoted aza-Michael addition of amines to conjugated alkenes in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.08.038openalex-snapshot
A new synthesis of acetamido phenols promoted by Ce(SO4)2
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.03.169openalex-snapshot
A simple and efficient approach to 1,3-aminoalcohols: application to the synthesis of (+)-negamycin
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.126openalex-snapshot
A three-component novel synthesis of 1-carbamato-alkyl-2-naphthol derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.059openalex-snapshot
Nanocrystalline copper(II) oxide catalyzed aza-Michael reaction and insertion of α-diazo compounds into N–H bonds of amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.116openalex-snapshot
Brønsted acidic ionic liquid as an efficient and reusable catalyst for one-pot synthesis of 1-amidoalkyl 2-naphthols under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.055openalex-snapshot
Atom-efficient and environment-friendly multicomponent synthesis of amidoalkyl naphthols catalyzed by P2O5
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.040openalex-snapshot
A new regio- and stereoselective synthesis of β-enamino ketones with 3-ethoxycyclobutanones and substituted amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.019openalex-snapshot
A simple protocol for the preparation of β-enamino ketones catalyzed by NbOPO4 under solvent free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.04.059openalex-snapshot
Pursuing effective Gram-negative antibiotics: The chemical synthesis of negamycin
inferred← citeshttps://doi.org/10.1016/s0022-1139(00)81029-5openalex-snapshot
An enzyme-assisted polymerization. Effect of the reaction medium for the controlled polymerization of fluoroamino acids
inferred← citeshttps://doi.org/10.1016/s0022-1139(00)83963-9openalex-snapshot
The synthesis of optically active building blocks carrying an α, α-dihalogeno-β, β, β-trifluoroethyl group
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00155-1openalex-snapshot
Organometallic Additions to β-substituted N-Boc-β-aminoaldehydes: a New Synthesis of Enantiomerically Pure 1,3-disubstituted N-Boc-1,3-aminoalcohols
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)81510-6openalex-snapshot
Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)82410-8openalex-snapshot
Enzymes in organic synthesis-29
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)86065-8openalex-snapshot
Stereoselective Synthesis of γ-hydroxy-α-amino acids via intramolecular amidomercuration
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)87306-3openalex-snapshot
Tetrahedron report number 203
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)90313-8openalex-snapshot
A new synthesis of both the enantiomers of 4-amino-3-hydroxybutanoic acid (gabob) and mm2 calculations for rotamers of the intermediate oxazolidin-2-on
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96102-2openalex-snapshot
Chelat- und nicht-chelat-kontrollierte reduktionen von β-amido-ketonen: Synthese nicht-racemischer 1,3-aminoalkohole mit pyrrolidinstruktur
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96136-8openalex-snapshot
A new approach to the synthesis of enantiomerically pure 2,3-diaminoacids through chiral imidazolidin-2-ones
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00131-xopenalex-snapshot
The reactivity of the N-Boc protecting group: an underrated feature
inferred← citeshttps://doi.org/10.1016/s0040-4020(95)01021-1openalex-snapshot
Enantioselective synthesis through enzymatic asymmetrization
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61332-1openalex-snapshot
An application of quinic acid to the synthesis of linear homochiral molecules: A synthesis of (+)-negamycin.
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61896-8openalex-snapshot
Immobilized porcine liver esterase: a convenient reagent for the preparation of chiral building blocks.
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74232-8openalex-snapshot
Stereoselective silver triflate-mediated iodocyclization of carbamates
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)80098-2openalex-snapshot
Oxazinone versus allene formation in the reaction of N-alkoxycarbonyliminium ions with propargyltrimethylsilane
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)80421-9openalex-snapshot
Synthesis of (+)-negamycin from D-glucose
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)86063-3openalex-snapshot
Enantioselective total synthesis of (+)-negamycin
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)92329-3openalex-snapshot
Palladium(II)-catalyzed oxidative aminocarbonylation of unsaturated carbamates
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)95353-xopenalex-snapshot
Enzyme-mediated asymmetric hydrolysis of α-benzyloxycarboxylic esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)95574-6openalex-snapshot
Mild and selective ring-cleavage of cyclic carbamates to amino alcohols
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)96301-9openalex-snapshot
Stereocontrolled synthesis of 6-epi-D-purpurosamine B by iodocyclocarbamation of a chiral Z-olefin derived from L-alanine and L-malic acid
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)96439-6openalex-snapshot
A new mode of cyclic carbamate formation via tert-butyldimethylsilyl carbamate. Stereoselective syntheses of statine and its analogue
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)99635-7openalex-snapshot
Reduction of 5,6-dihydro-2H-1,3-oxazines. A simple approach to 1,3-aminoalcohols from 2-aza-1,3-dienes
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01904-9openalex-snapshot
One-pot highly stereoselective reduction of β-keto amides to syn -γ-aminols
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)81230-2openalex-snapshot
Creation of novel chiral synthons with enzymes and applications to natural product synthesis. 15. Efficient introduction of chiral centers into cyclohexane ring
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91124-4openalex-snapshot
A stereocontrolled synthesis of (−)-bestatin from an acyclic allylamine by iodocyclocarbamation
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01545-9openalex-snapshot
Stereoselective reduction of enaminones to syn γ-aminoalcohols
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01349-xopenalex-snapshot
Stereocontrolled reductive amination of 3-hydroxy ketones
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01364-1openalex-snapshot
Enantiospecific synthesis of 6-substituted N-aryl-1,3-oxazin-2-ones
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02698-7openalex-snapshot
B-(2-Azido-2-propenyl)-1,3,2-dioxaborinane: A novel reagent for allylboration
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00778-9openalex-snapshot
Synthesis of amino allenes via reaction of α-aminoalkylcuprates with propargyl substrates
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)01954-1openalex-snapshot
Asymmetric synthesis of a highly functionalized β-amino acid: the key amino acid of sperabillins B and D
inferred← citeshttps://doi.org/10.1016/s0957-4166(00)80070-1openalex-snapshot
Practical enzymatic route to optically active 3-hydroxyamides. Synthesis of 1,3-aminoalcohols
inferred← citeshttps://doi.org/10.1016/s0957-4166(00)86049-8openalex-snapshot
Enzymatic synthesis of 3-hydroxybutyramides and their conversion to optically active 1,3-aminoalcohols
inferred← citeshttps://doi.org/10.1016/s0957-4166(01)00058-1openalex-snapshot
A facile preparation of (±)-β-hydroxy nitriles and their enzymatic resolution with lipases
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(02)00869-8openalex-snapshot
Desymmetrization of dimethyl 3-substituted glutarates through enzymatic ammonolysis and aminolysis reactions
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00016-6openalex-snapshot
Bioreduction of 2-oxocyclopentanecarboxamides: syntheses of optically active 2-aminomethyl- and 2-aminocyclopentanols
inferred← citeshttps://doi.org/10.1016/s0960-894x(03)00393-7openalex-snapshot
N- and C-terminal modifications of negamycin
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60029-2openalex-snapshot
One-pot synthesis of 1-amidoalkyl-2-naphthols catalyzed by melamine-Br3 under solvent-free conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01692openalex-snapshot
Synthesis of a 3,4-Dihydro-1,3-oxazin-2-ones Skeleton via an Intermolecular [4 + 2] Process of N-Acyliminium Ions with Ynamides/Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03400openalex-snapshot
The Synthesis of Functionalized 3-Aryl- and 3-Heteroaryloxazolidin-2-ones and Tetrahydro-3-aryl-1,3-oxazin-2-ones via the Iodocyclocarbamation Reaction: Access to Privileged Chemical Structures and Scope and Limitations of the Method
inferred← citeshttps://doi.org/10.1021/acs.oprd.5b00163openalex-snapshot
An Efficient and Waste-Minimized One-Pot Procedure for the Preparation of N-Boc-γ-amino Alcohols Starting from α,β-Unsaturated Ketones in Flow
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00407openalex-snapshot
Acid-Mediated Ring Expansion of 2,2-Disubstituted Azetidine Carbamates to 6,6-Disubstituted 1,3-Oxazinan-2-ones
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/acsinfecdis.5c00843openalex-snapshot
Negamycin: Nature’s Forgotten Antibiotic
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5b00091openalex-snapshot
Lignosulfonic Acid: A Renewable and Effective Biomass-Based Catalyst for Multicomponent Reactions
inferred← citeshttps://doi.org/10.1021/cs5010695openalex-snapshot
Phenalenyl in a Different Role: Catalytic Activation through the Nonbonding Molecular Orbital
inferred← citeshttps://doi.org/10.1021/ja107857vopenalex-snapshot
Enantioselective Synthesis of syn- and anti-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation
inferred← citeshttps://doi.org/10.1021/ja506031hopenalex-snapshot
Triple Role of Phenylselenonyl Group Enabled a One-Pot Synthesis of 1,3-Oxazinan-2-ones From α-Isocyanoacetates, Phenyl Vinyl Selenones, and Water
inferred← citeshttps://doi.org/10.1021/ja9731074openalex-snapshot
Highly Regio- and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ,δ-Unsaturated Amino Acids
inferred← citeshttps://doi.org/10.1021/jacs.4c13538openalex-snapshot
Catalytic Asymmetric Cycloaddition of Olefins with In Situ Generated N-Boc-Formaldimine
inferred← citeshttps://doi.org/10.1021/jacs.9b05221openalex-snapshot
Iron-Catalyzed Anti-Markovnikov Hydroamination and Hydroamidation of Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/jo0001582openalex-snapshot
Isolation, Structural Characterization, and Synthesis of a Naturally Occurring Bisfuranopseudopterane Ether: Biskallolide A. Evidence for a Carbocation Intermediate during the Facile Conversion of Kallolide A and Isokallolide A into Various Solvolysis Products
inferred← citeshttps://doi.org/10.1021/jo026254fopenalex-snapshot
Synthesis of (R)-3,4-Diaminobutanoic Acid by Desymmetrization of Dimethyl 3-(Benzylamino)glutarate through Enzymatic Ammonolysis
inferred← citeshttps://doi.org/10.1021/jo026550sopenalex-snapshot
Bismuth Nitrate-Catalyzed Versatile Michael Reactions
inferred← citeshttps://doi.org/10.1021/jo0343329openalex-snapshot
Isolation and Characterization of Kallosin A, a Novel Rearranged Pseudopterane Diterpenoid from the Caribbean Sea Plume Pseudopterogorgia kallos (Bielschowsky)
inferred← citeshttps://doi.org/10.1021/jo048990kopenalex-snapshot
Rhodium(II)-Catalyzed Aziridination of Allyl-Substituted Sulfonamides and Carbamates
inferred← citeshttps://doi.org/10.1021/jo951920gopenalex-snapshot
A Novel Norditerpene from the Caribbean Sea Plume Pseudopterogorgia acerosa (Pallas)
inferred← citeshttps://doi.org/10.1021/jo970898jopenalex-snapshot
Regiocontrolled Iodoaminocyclization Reaction of an Ambident Nucleophile Mediated by Basic Metallic Reagent
inferred← citeshttps://doi.org/10.1021/jo971884gopenalex-snapshot
The First Cembrane−Pseudopterane Cycloisomerization
inferred← citeshttps://doi.org/10.1021/jo980256bopenalex-snapshot
Pinnatins A−E: Marine Diterpenes of the Rare Gersolane Class Derived from a Photochemically Induced Rearrangement of a Conjugated 2,5-Bridged Furanocembrane Precursor
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