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A Novel Chiral Super-Lewis Acidic Catalyst for Enantioselective Synthesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0957-4166(94)80111-8openalex-snapshot
Diastereo and enantioselective entry to β-amino esters by hydride reduction of homochiral β-enamino esters.
inferredcites →https://doi.org/10.1016/s0040-4039(00)61781-1openalex-snapshot
Highly enantioselective catalytic Diels-Alder addition promoted by a chiral bis(oxazoline)-magnesium complex
inferredcites →https://doi.org/10.1021/cr00013a013openalex-snapshot
Catalytic asymmetric Diels Alder reactions
inferredcites →https://doi.org/10.1021/ja00002a081openalex-snapshot
Designed catalyst for enantioselective Diels-Alder addition from a C2-symmetric chiral bis(oxazoline)-iron(III) complex
inferredcites →https://doi.org/10.1021/ja00046a065openalex-snapshot
X-ray crystallographic and NMR studies on the origins of high enantioselectivity in Diels-Alder reactions catalyzed by a chiral diazaaluminolidine
inferredcites →https://doi.org/10.1021/ja00087a062openalex-snapshot
Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid
inferredcites →https://doi.org/10.1021/ja00105a074openalex-snapshot
First Example of a Highly Enantioselective Catalytic Diels-Alder Reaction of an Achiral C2v-Symmetric Dienophile and an Achiral Diene
inferredcites →https://doi.org/10.1021/ja00142a051openalex-snapshot
Enantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder Methodology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cobalt(Ii) Catalyzed Michael-Type Hydroarylamination of Activated Olefins
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Contributions to the Coordination and Structural Chemistry of Gallium(III) and Indium(III) Halides: Complexes with Bi- and Tridentate Tertiary Phosphanes
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Der katalytische enantioselektive Aufbau von Molekülen mit quartären Kohlenstoff-Stereozentren
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Chromatographische Enantiomerentrennung an Polysaccharidderivaten
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Moderne Varianten der Mannich-Reaktion
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Low Coordinated Group 13 Chelates
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Enantioselective Diels−Alder Reactions of Optically Active (Buta-1,3-dien-2-yl)(salen)cobalt(III) Complexes
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Katalytische enantioselektive Diels-Alder-Reaktionen: Methoden, mechanistische Grundlagen, Reaktionswege und Anwendungen
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Catalytic Enantioselective Diels-Alder Reactions: Methods, Mechanistic Fundamentals, Pathways, and Applications
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IntermolecularCyclization Reactions to form Carbocycles
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Chiral auxiliaries and catalysts
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Chiral auxiliaries and catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub3openalex-snapshot
Chiral auxiliaries and catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub4openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub5openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub6openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9781118662083.cot02-008openalex-snapshot
Formation of Alkenes by Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/9781118846919.ch1openalex-snapshot
Toward Ideal Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0271openalex-snapshot
Low Coordinated Group 13 Chelates
inferred← citeshttps://doi.org/10.1002/9783527691036.hsscvol6030openalex-snapshot
Heterogeneous Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.200404361openalex-snapshot
Cu(acac)2 Immobilized in Ionic Liquids: A Recoverable and Reusable Catalytic System for Aza‐Michael Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201000428openalex-snapshot
Reusable Chiral Dicationic Chromium(III) Salen Catalysts for Aminolytic Kinetic Resolution of trans‐Epoxides
inferred← citeshttps://doi.org/10.1002/ajoc.202100092openalex-snapshot
Organoboron Compounds Towards Asymmetric Pericyclic Reaction; Exploitation to Bioactive Molecule Synthesis
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α‐CH‐Acidität und Reaktivität von Lewis‐Säure‐Base‐Komplexen in der Gasphase
inferred← citeshttps://doi.org/10.1002/ange.200461319openalex-snapshot
Oxazaborolidine‐Derived Lewis Acid Assisted Lewis Acid as a Moisture‐Tolerant Catalyst for Enantioselective Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/ange.200500154openalex-snapshot
Protonierte chirale Katalysatoren: vielseitige Hilfsmittel für die asymmetrische Synthese
inferred← citeshttps://doi.org/10.1002/ange.200500402openalex-snapshot
Borinium‐, Borenium‐ und Boroniumionen: Synthese, Reaktivität, Anwendung
inferred← citeshttps://doi.org/10.1002/ange.200703616openalex-snapshot
Synthese und strukturelle Charakterisierung eines stabilen dimeren Bor(II)‐Dikations
inferred← citeshttps://doi.org/10.1002/ange.200801408openalex-snapshot
Asymmetric Diels–Alder Reactions of α,β‐Unsaturated Aldehydes Catalyzed by a Diarylprolinol Silyl Ether Salt in the Presence of Water
inferred← citeshttps://doi.org/10.1002/ange.200805374openalex-snapshot
Enantioselektive Katalyse mit kationischen Oxazaborolidinen
inferred← citeshttps://doi.org/10.1002/ange.201106497openalex-snapshot
Enantioselective Diels–Alder Reactions with Anomalous endo/exo Selectivities Using Conformationally Flexible Chiral Supramolecular Catalysts
inferred← citeshttps://doi.org/10.1002/ange.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/ange.201710782openalex-snapshot
Die Schöne (WCA) und das (kationische) Biest: Neues aus der Chemie von und mit schwach koordinierenden Anionen
inferred← citeshttps://doi.org/10.1002/anie.199722301openalex-snapshot
Enhanced α‐CH Acidity and Reactivity of Lewis Acid–Base Complexes in the Gas Phase
inferred← citeshttps://doi.org/10.1002/anie.200461319openalex-snapshot
Oxazaborolidine‐Derived Lewis Acid Assisted Lewis Acid as a Moisture‐Tolerant Catalyst for Enantioselective Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/anie.200500154openalex-snapshot
Protonated Chiral Catalysts: Versatile Tools for Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200500402openalex-snapshot
Borinium, Borenium, and Boronium Ions: Synthesis, Reactivity, and Applications
inferred← citeshttps://doi.org/10.1002/anie.200703616openalex-snapshot
Synthesis and Structural Characterization of a Stable Dimeric Boron(II) Dication
inferred← citeshttps://doi.org/10.1002/anie.200801408openalex-snapshot
Asymmetric Diels–Alder Reactions of α,β‐Unsaturated Aldehydes Catalyzed by a Diarylprolinol Silyl Ether Salt in the Presence of Water
inferred← citeshttps://doi.org/10.1002/anie.200805374openalex-snapshot
Enantioselective Catalysis Based on Cationic Oxazaborolidines
inferred← citeshttps://doi.org/10.1002/anie.201106497openalex-snapshot
Enantioselective Diels–Alder Reactions with Anomalous endo/exo Selectivities Using Conformationally Flexible Chiral Supramolecular Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/anie.201710782openalex-snapshot
Taming the Cationic Beast: Novel Developments in the Synthesis and Application of Weakly Coordinating Anions
inferred← citeshttps://doi.org/10.1002/aoc.3031openalex-snapshot
NH2SO3H–SiO2 as a new water‐compatible, recyclable heterogeneous catalyst for the synthesis of novel (α,β‐unsaturated) β‐amino ketones via aza‐Michael reaction
inferred← citeshttps://doi.org/10.1002/aoc.3457openalex-snapshot
Lanthanum immobilized on chitosan: a highly efficient heterogeneous catalyst for facile synthesis of novel (α,β‐unsaturated) β‐aminoketones
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Synthesis and Characterization of Silica@Copper Core–Shell Nanoparticles: Application for Conjugate Addition Reactions
inferred← citeshttps://doi.org/10.1002/cbdv.201400060openalex-snapshot
endo/exo Stereoselectivity in DielsAlder Reactions of α,β‐Dialkylated Conjugated Enals to Cyclic 1,3‐Dienes: Intermediates in the Synthesis of (−)‐β‐Santalol and Its Analogs
inferred← citeshttps://doi.org/10.1002/cctc.201200912openalex-snapshot
Synthesis of Chiral Ligands with Multiple Stereogenic Centers and Their Application in Titanium(IV)‐Catalyzed Enantioselective Desymmetrization of meso‐Epoxides
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Interplay between Solvent and Counteranion Stabilization of Highly Unsaturated Rhodium( III ) Complexes: Facile Unsaturation‐Induced Dearomatization
inferred← citeshttps://doi.org/10.1002/chem.200600851openalex-snapshot
Ruthenium–Lewis Acid Catalyzed Asymmetric Diels–Alder Reactions between Dienes and α,β‐Unsaturated Ketones
inferred← citeshttps://doi.org/10.1002/chem.200900884openalex-snapshot
Chemoselective Synthesis of Substituted Imines, Secondary Amines, and β‐Amino Carbonyl Compounds from Nitroaromatics through Cascade Reactions on Gold Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201802698openalex-snapshot
Lewis Superacids: Classifications, Candidates, and Applications
inferred← citeshttps://doi.org/10.1002/chin.199638047openalex-snapshot
ChemInform Abstract: A Novel Chiral Super‐Lewis Acidic Catalyst for Enantioselective Synthesis.
inferred← citeshttps://doi.org/10.1002/chir.20906openalex-snapshot
Synthesis of enantiopure trans‐N‐Boc‐3‐aminobicyclo[2.2.2]octane‐2‐carboxylic acids and their bicyclic 1,3‐amino alcohol derivatives via the [4+2] cycloaddition of 1,3‐cyclohexadiene to a chiral β‐nitroacrylate
inferred← citeshttps://doi.org/10.1002/cjoc.200990064openalex-snapshot
Aza‐Michael Addition of Isatin and Phthalimide to Symmetrical Fumaric Esters in Ionic Liquid Media
inferred← citeshttps://doi.org/10.1002/cjoc.201100351openalex-snapshot
Environmental Friendly Synthesis of Novel Isatin Ketal and Isatin Schiff Base Derivatives Using Michael Addition Reaction under Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/cplu.201300196openalex-snapshot
Iron Nanoparticles Supported on Graphene Oxide: A Robust, Magnetically Separable Heterogeneous Catalyst for the Oxidative Cyanation of Tertiary Amines
inferred← citeshttps://doi.org/10.1002/ejic.201000972openalex-snapshot
Influence of a Redox‐Active Phosphane Ligand on the Oxidations of a Diiron Core Related to the Active Site of Fe‐Only Hydrogenase
inferred← citeshttps://doi.org/10.1002/ejoc.200600999openalex-snapshot
A Basic Ionic Liquid as Catalyst and Reaction Medium: A Rapid and Simple Procedure for Aza‐Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.200800099openalex-snapshot
Highly Enantioselective Syntheses of Chiral β‐Amino Alcohols in the Presence of Chiral TiIV Schiff Base Complexes as Catalysts
inferred← citeshttps://doi.org/10.1002/hc.21112openalex-snapshot
Selected Reactions of Diethyl (E)‐1‐(bromomethyl)‐2‐cyanovinylphosphonate with Secondary and Tertiary Amines
inferred← citeshttps://doi.org/10.1002/hlca.200490054openalex-snapshot
Asymmetric Syntheses of 2‐(1‐Aminoethyl)phenols
inferred← citeshttps://doi.org/10.1002/hlca.200790238openalex-snapshot
Synthesis of Spiropyrimidodiazepines and Spirodiazepinopurines by Tandem Nitroso‐ene/Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/jctb.6203openalex-snapshot
Lipase‐catalyzed aza‐Michael addition of amines to acrylates in supercritical carbon dioxide
inferred← citeshttps://doi.org/10.1002/jlac.199719970520openalex-snapshot
Chemo‐, Regio‐, and Stereoselective Diels–Alder Reaction of Ambident Dienophilic Monothiomaleimide
inferred← citeshttps://doi.org/10.1002/slct.201701103openalex-snapshot
Experimental and Theoretical Investigation of the Reaction of Amines with Methyl Propiolate
inferred← citeshttps://doi.org/10.1002/slct.201804070openalex-snapshot
Aza‐Michael Addition of 5‐Substituted Tetrazole Catalysed By a Novel Nanoparticle Solid Base Catalyst Involving a Layered Zinc Hydroxide Supported on a Ferrite Core
inferred← citeshttps://doi.org/10.1007/bf03246110openalex-snapshot
Some applications of zirconium(IV) tetrachloride (ZrCl4) and zirconium(IV) oxydichloride octahydrate (ZrOCl2.8H2O) as catalysts or reagents in organic synthesis
inferred← citeshttps://doi.org/10.1007/s10562-008-9646-7openalex-snapshot
An Efficient Protocol for Aza-Michael Addition Reactions Under Solvent-Free Condition Employing Sulfated Zirconia Catalyst
inferred← citeshttps://doi.org/10.1007/s10904-021-02006-0openalex-snapshot
Catalytic Application of Ceric Ammonium Nitrate-Stabilized Maghemite Nanoparticles (CAN-γ-Fe2O3) for Ultrasound Assisted Synthesis of β-Amino Derivatives
inferred← citeshttps://doi.org/10.1007/s11164-012-0575-0openalex-snapshot
An environmentally benign protocol: catalyst-free Michael addition of aromatic amines to α,β-unsaturated ketones in glycerol
inferred← citeshttps://doi.org/10.1007/s11224-021-01735-9openalex-snapshot
Michael addition of ethyl anthranilate and phenyl monothioanthranilate to acetylenic esters: experimental and theoretical results
inferred← citeshttps://doi.org/10.1007/s13738-023-02858-yopenalex-snapshot
Michael addition reaction on 5,6-dimethoxy-2-methylene-2,3-dihydro-1H-inden-1-one: checking the products stability and evaluation of retro Michael reaction possibility
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00344-8openalex-snapshot
Enantioselective Diels-Alder reactions catalyzed by chiral magnesium lewis acids prepared from hydroxysulfoxides
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00002-9openalex-snapshot
Ligands, Reagents, and Methods in Organometallic Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-08-044860-2.00006-4openalex-snapshot
Cycloadditions and Rearrangements
inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00101-xopenalex-snapshot
Iridium Pincer Complexes: Coordination, Reactivity and Catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00102-1openalex-snapshot
Rhodium Pincer Complexes: Coordination, Reactivity and Catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-443-33403-0.00002-1openalex-snapshot
On the origins of local positive potentials on group 13 central atoms and the ouroboric cyclization of heteroorganic chains
inferred← citeshttps://doi.org/10.1016/b978-008043404-9/50024-3openalex-snapshot
Transferring Chirality in Homogeneous Catalysis
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00819-1openalex-snapshot
Six-membered Rings with Two or More Heteroatoms with at least One Boron
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.03.025openalex-snapshot
Asymmetric reduction of 3-aryl-3-keto esters using Rhizopus species
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.03.035openalex-snapshot
γ-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists
inferred← citeshttps://doi.org/10.1016/j.carres.2006.04.021openalex-snapshot
DBU assisted expeditious synthesis of glycosyl dienes via glycosylated β-hydroxy esters
inferred← citeshttps://doi.org/10.1016/j.crci.2010.07.007openalex-snapshot
Regiospecific synthesis of 1,2-aminoalcohol by ring-opening of racemic styrene oxide in presence of Lewis acids
inferred← citeshttps://doi.org/10.1016/j.ica.2026.123411openalex-snapshot
A chemists' guide to salt metathesis and its applications
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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.jorganchem.2008.10.004openalex-snapshot
Straightforward access to oxazaborines, diazaborinones and triazaborines by reactions of β-enaminoamides with 4-methylbenzenediazonium tetraphenylborate
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.03.018openalex-snapshot
Addition of dimethylaluminium chloride to N,N′-Disubstituted carbodiimides
inferred← citeshttps://doi.org/10.1016/j.jscs.2010.12.005openalex-snapshot
Synthesis, characterization and coordination chemistry of substituted β-amino dicarbonyls
inferred← citeshttps://doi.org/10.1016/j.micromeso.2012.08.015openalex-snapshot
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.2014.06.031openalex-snapshot
Room temperature solvent free aza-Michael reactions over nano-cage mesoporous materials
inferred← citeshttps://doi.org/10.1016/j.molcatb.2007.12.003openalex-snapshot
Lipase-catalyzed resolution of 1-chloro-3-[(4-morpholin-4-yl-1,2,5-thiadiazole-3-yl)oxy]propan-2-ol
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.04.009openalex-snapshot
Synthesis, spectroscopic analysis (FT-IR, UV and NMR) and DFT analysis of novel prodrugs of pregnane, their apoptotic activity in cervical cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130691openalex-snapshot
Synthesis of limonene β-amino alcohol from (R)-(+)-α-methylbenzylamine and (+)-limonene 1,2-epoxide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.145030openalex-snapshot
Microwave-mediated transformation of 1,3-dibenzoylpropane into N-heteroalkyl-2,6-diphenylpiperidines: Preferential formation of cis-Isomers and structural studies
inferred← citeshttps://doi.org/10.1016/j.tet.2005.09.013openalex-snapshot
The stereoselective synthesis of α-substituted β-amino secondary alcohols based on the proline-mediated, asymmetric, three-component Mannich reaction and its application to the formal total synthesis of nikkomycins B and Bx
inferred← citeshttps://doi.org/10.1016/j.tet.2005.09.117openalex-snapshot
[HP(HNCH2CH2)3N]NO3: an efficient homogeneous and solid-supported promoter for aza and thia-Michael reactions and for Strecker reactions
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.2014.06.003openalex-snapshot
Tandem Michael addition of amines to maleic anhydride and 1,3-prototropic shift: experimental and theoretical results
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.09.026openalex-snapshot
Rhizopus arrhizus mediated asymmetric reduction of alkyl 3-oxobutanoates
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.2006.04.019openalex-snapshot
Lipase-mediated resolution of 3-hydroxy-4-trityloxybutanenitrile: synthesis of 2-amino alcohols, oxazolidinones and GABOB
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.11.068openalex-snapshot
The first N,N′-ditosyl-substituted cyclic boron cation, stabilized by neighboring-group participation by two sulfonyl groups, and the alternative, stabilized by polar solvents
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.2006.10.142openalex-snapshot
Significant rate acceleration of the aza-Michael reaction in water
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.2014.03.013openalex-snapshot
An experimental and theoretical reinvestigation of the Michael addition of primary and secondary amines to dimethyl acetylenedicarboxylate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.089openalex-snapshot
Catalytic enantioselective C(sp3)H functionalization: intramolecular benzylic [1,5]-hydride shift
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.051openalex-snapshot
Asymmetric Diels–Alder reactions of N-allenoyloxazolidinones catalyzed by Cu(II)–bis(oxazoline) complexes
inferred← citeshttps://doi.org/10.1016/s0021-9673(98)00471-3openalex-snapshot
High-performance liquid chromatographic separation of enantiomers of cyclic 1,3-amino alcohol derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00433-xopenalex-snapshot
Can a chiral catalyst containing the same ligand/metal components promote the formation of both enantiomers enantioselectively? The bis(oxazoline)-magnesium perchlorate-catalyzed asymmetric Diels-Alder reaction
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)01038-7openalex-snapshot
Zirconocene-catalyzed epoxy ester - ortho ester rearrangement: A new method for the protection of polyfunctionalized carboxylic acids and the asymmetric synthesis of ortho esters
inferred← citeshttps://doi.org/10.1016/s0040-4020(98)00303-2openalex-snapshot
Chiral Lewis acid controlled Diels-Alder reaction: Factors affecting the stereoselective formation of both enantiomers in the bis(oxazoline)-magnesium catalyzed process
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00086-1openalex-snapshot
Chiral (E,E)-1,4-dialkoxy-1,3-butadienes. 2. Conformational studies and Diels-Alder reactions with symmetric dienophiles
inferred← citeshttps://doi.org/10.1016/s0040-4039(96)02249-6openalex-snapshot
The application of the formyl CH--O hydrogen bond postulate to the understanding of enantioselective reactions involving chiral boron lewis acids and aldehydes
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01287-2openalex-snapshot
Enantioselective Diels-Alder reactions between cyclopentadiene and α,β-acetylenic aldehydes catalyzed by a chiral super Lewis acid
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00841-2openalex-snapshot
Synthesis of new chiral σ2λ2-phosphenium cations
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(97)00160-2openalex-snapshot
A practical synthesis of enantiopure ethyl cis-2-amino-1-cyclohexanecarboxylate via asymmetric reductive amination methodology
inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00019-6openalex-snapshot
Lipase-catalysed resolution of 2-dialkylaminomethylcyclohexanols
inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00236-5openalex-snapshot
Enzymatic resolution of alicyclic 1,3-amino alcohols in organic media
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00189-5openalex-snapshot
Enzymatic resolution of 2-dialkylaminomethylcyclopentanols and -cycloheptanols
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00463-2openalex-snapshot
Enantioselective synthesis of cyclopropane aminoalcohols containing quaternary stereogenic centers
inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80028-9openalex-snapshot
The Chemistry of 2-Aminocyclopentanecarboxylic Acid
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c02073openalex-snapshot
[B–Cl–B]+ Cations: Chloroborane Masked Chiral Borenium Ions
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b00053openalex-snapshot
Terpyridine Molybdenum Dinitrogen Chemistry: Synthesis of Dinitrogen Complexes That Vary by Five Oxidation States
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b00657openalex-snapshot
Stable Open-Shell Phosphorane Based on a Redox-Active Amidodiphenoxide Scaffold
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02914openalex-snapshot
Probing Carbocatalytic Activity of Carbon Nanodots for the Synthesis of Biologically Active Dihydro/Spiro/Glyco Quinazolinones and Aza-Michael Adducts
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03090openalex-snapshot
exo/endo Selectivity Control in Diels–Alder Reactions of Geminal Bis(silyl) Dienes: Theoretical and Experimental Studies
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00210openalex-snapshot
Room-Temperature Benzylic Alkylation of Benzylic Carbonates: Improvement of Palladium Catalyst and Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00170openalex-snapshot
Flash Communication: On “Ag[BArF4]” and an Expedient Synthesis of [Ag(C6H6)3][BArF4]
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01343openalex-snapshot
Expanding the Chiral Monoterpene Pool: Enantioselective Diels–Alder Reactions of α-Acyloxy Enones
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03147openalex-snapshot
Oxathiaborolium: A Type of Chiral Lewis Acid Catalyst and Its Application in Catalytic and Highly Enantioselective Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02630openalex-snapshot
NH 2 -Directed C–H Alkenylation of 2-Vinylanilines with Vinylbenziodoxolones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03193openalex-snapshot
Direct, Mild, and General n-Bu4NBr-Catalyzed Aldehyde Allylsilylation with Allyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03939openalex-snapshot
Asymmetric Diels–Alder Reaction of α,β-Unsaturated Oxazolidin-2-one Derivatives Catalyzed by a Chiral Fe(III)-Bipyridine Diol Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02280openalex-snapshot
Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions
inferred← citeshttps://doi.org/10.1021/acscatal.4c02708openalex-snapshot
Benchtop-Stable Carbyl Iminopyridyl Ni II Complexes for Olefin Polymerization
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5b00542openalex-snapshot
Sustainable and Versatile CuO/GNS Nanocatalyst for Highly Efficient Base Free Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ar970230ropenalex-snapshot
Carboranes: A New Class of Weakly Coordinating Anions for Strong Electrophiles, Oxidants, and Superacids
inferred← citeshttps://doi.org/10.1021/cr000456zopenalex-snapshot
The Chemistry of 2-Aminocycloalkanecarboxylic Acids
inferred← citeshttps://doi.org/10.1021/cr050065qopenalex-snapshot
1,3-Aminoalcohols and Their Derivatives in Asymmetric Organic Synthesis
inferred← citeshttps://doi.org/10.1021/cr1002084openalex-snapshot
Heterogeneous Catalysts for the One-Pot Synthesis of Chemicals and Fine Chemicals
inferred← citeshttps://doi.org/10.1021/cr200133copenalex-snapshot
Cationic Tricoordinate Boron Intermediates: Borenium Chemistry from the Organic Perspective
inferred← citeshttps://doi.org/10.1021/ic102590fopenalex-snapshot
Ethylene Sensing by Silver(I) Salt-Impregnated Luminescent Films
inferred← citeshttps://doi.org/10.1021/ic800876popenalex-snapshot
Synthesis and Structure of a Ferrocenylboron Dication
inferred← citeshttps://doi.org/10.1021/ic961164copenalex-snapshot
Synthesis and Structure of the Thallium(I) Salt of the Tetrakis{3,5-bis(trifluoromethyl)phenyl}borate Anion
inferred← citeshttps://doi.org/10.1021/ic961455lopenalex-snapshot
Base Effects on the Formation of Four- and Five-Coordinate Cationic Aluminum Complexes
inferred← citeshttps://doi.org/10.1021/ic971595aopenalex-snapshot
Chelated Borates: Synthesis, Reactivity, and Cation Formation
inferred← citeshttps://doi.org/10.1021/ja016017eopenalex-snapshot
Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Allylation and Propargylation of Aldehydes
inferred← citeshttps://doi.org/10.1021/ja025848xopenalex-snapshot
Asymmetric Diels−Alder Reactions Catalyzed by a Triflic Acid Activated Chiral Oxazaborolidine
inferred← citeshttps://doi.org/10.1021/ja027468hopenalex-snapshot
Broad-Spectrum Enantioselective Diels−Alder Catalysis by Chiral, Cationic Oxazaborolidines
inferred← citeshttps://doi.org/10.1021/ja1018628openalex-snapshot
Stereoselective Construction of Halogenated Quaternary Stereogenic Centers via Catalytic Asymmetric Diels−Alder Reaction
inferred← citeshttps://doi.org/10.1021/ja309905jopenalex-snapshot
Total Synthesis of (±)-Maoecrystal V
inferred← citeshttps://doi.org/10.1021/ja506502popenalex-snapshot
Diiodoindium(III) Cation, InI2+, a Potent Yneophile. Generation and Application to Cationic Cyclization by Selective π-Activation of C≡C
inferred← citeshttps://doi.org/10.1021/ja508804nopenalex-snapshot
Allosteric Regulation of Supramolecular Oligomerization and Catalytic Activity via Coordination-Based Control of Competitive Hydrogen-Bonding Events
inferred← citeshttps://doi.org/10.1021/ja904535fopenalex-snapshot
Alkylation of Dinitrogen in [(HIPTNCH2CH2)3N]Mo Complexes (HIPT = 3,5-(2,4,6-i-Pr3C6H2)2C6H3)
inferred← citeshttps://doi.org/10.1021/ja973444copenalex-snapshot
A New Magnesium-Catalyzed Doubly Diastereoselective anti-Aldol Reaction Leads to a Highly Efficient Process for the Total Synthesis of Lactacystin in Quantity
inferred← citeshttps://doi.org/10.1021/ja9804518openalex-snapshot
Gas-Phase Negative Ion Chemistry of Lewis Acid−Base Complexes
inferred← citeshttps://doi.org/10.1021/ja981021kopenalex-snapshot
Synthesis and Application of the First Chiral and Highly Lewis Acidic Silyl Cationic Catalyst
inferred← citeshttps://doi.org/10.1021/ja992104jopenalex-snapshot
Synthesis and Structures of Cationic Aluminum and Gallium Amidinate Complexes
inferred← citeshttps://doi.org/10.1021/jacs.5b09689openalex-snapshot
Unique Steric Effect of Geminal Bis(silane) To Control the High Exo-selectivity in Intermolecular Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/jacs.5b11476openalex-snapshot
Activation of Chiral (Salen)AlCl Complex by Phosphorane for Highly Enantioselective Cyanosilylation of Ketones and Enones
inferred← citeshttps://doi.org/10.1021/jacs.8b10522openalex-snapshot
Enantioselective Conversion of Oligoprenol Derivatives to Macrocycles in the Germacrene, Cembrene, and 18-Membered Cyclic Sesterterpene Series
inferred← citeshttps://doi.org/10.1021/jm049530mopenalex-snapshot
Discovery of CC Chemokine Receptor-3 (CCR3) Antagonists with Picomolar Potency
inferred← citeshttps://doi.org/10.1021/jo0108764openalex-snapshot
Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica Gel
inferred← citeshttps://doi.org/10.1021/jo026550sopenalex-snapshot
Bismuth Nitrate-Catalyzed Versatile Michael Reactions
inferred← citeshttps://doi.org/10.1021/jo035508+openalex-snapshot
Synthesis and Structural Characterization of Trivalent Amino Acid Derived Chiral Phosphorus Compounds
inferred← citeshttps://doi.org/10.1021/jo4012656openalex-snapshot
Asymmetric Aminolytic Kinetic Resolution of Racemic Epoxides Using Recyclable Chiral Polymeric Co(III)-Salen Complexes: A Protocol for Total Utilization of Racemic Epoxide in the Synthesis of (R)-Naftopidil and (S)-Propranolol
inferred← citeshttps://doi.org/10.1021/jo401921fopenalex-snapshot
Oxidation Products of Doubly Trimethylene-Bridged Tetrabenzylp-Phenylenediamine Paracyclophane
inferred← citeshttps://doi.org/10.1021/jo9621276openalex-snapshot
Enantioselective Diels−Alder Reaction Using Chiral Mg Complexes Derived from Chiral 2-[2-[(Alkyl- or 2-[2-[(Arylsulfonyl)amino]phenyl]-4-phenyl-1,3-oxazoline
inferred← citeshttps://doi.org/10.1021/jo970171vopenalex-snapshot
First Enantioselective Catalytic Diels−Alder Reaction of Dienes and Acetylenic Aldehydes: Experimental and Theoretical Evidence for the Predominance of Exo-Transition Structure
inferred← citeshttps://doi.org/10.1021/ol034706kopenalex-snapshot
A New Cationic, Chiral Catalyst for Highly Enantioselective Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/ol500699copenalex-snapshot
Unravelling a New Class of Chiral Organocatalyst for Asymmetric Ring-Opening Reaction of Meso Epoxides with Anilines
inferred← citeshttps://doi.org/10.1021/ol703071copenalex-snapshot
Proximity-Assisted Cycloaddition ReactionsFacile Lewis Acid-Mediated Synthesis of Diversely Functionalized Bicyclic Tetrazoles
inferred← citeshttps://doi.org/10.1021/om010578xopenalex-snapshot
Cationic Indium Alkyl Complexes Incorporating Aminotroponiminate Ligands
inferred← citeshttps://doi.org/10.1021/om0201011openalex-snapshot
Neutral and Cationic Aluminum Complexes Supported by Sterically Bulky Amidinate Ligands
inferred← citeshttps://doi.org/10.1021/om0306729openalex-snapshot
Thallium Perfluorotetraphenylborate
inferred← citeshttps://doi.org/10.1021/om034381bopenalex-snapshot
3,5-Dialkyl Effect on Enantioselectivity in Pd Chemistry: Applications Involving Both Bidentate and Monodentate Auxiliaries
inferred← citeshttps://doi.org/10.1021/om050818zopenalex-snapshot
Non-Redox-Assisted Oxygen−Oxygen Bond Homolysis in Titanocene Alkylperoxide Complexes: [Cp2TiIV(η1-OOtBu)L]+/0, L = Cl-, OTf-, Br-, OEt2, Et3P
inferred← citeshttps://doi.org/10.1021/om061154bopenalex-snapshot
Mono(arene) Complexes of Thallium(I) Supported by a Weakly Coordinating Anion
inferred← citeshttps://doi.org/10.1021/om1000925openalex-snapshot
Mechanism of the Reaction of Vinyl Chloride with (α-diimine)PdMe+ Species
inferred← citeshttps://doi.org/10.1021/om5002815openalex-snapshot
Structure and Spectroelectrochemical Response of Arene–Ruthenium and Arene–Osmium Complexes with Potentially Hemilabile Noninnocent Ligands
inferred← citeshttps://doi.org/10.1021/om800034topenalex-snapshot
B−C Bond Cleavage of BArFAnion Upon Oxidation of Rhodium(I) with AgBArF. Phosphinite Rhodium(I), Rhodium(II), and Rhodium(III) Pincer Complexes
inferred← citeshttps://doi.org/10.1021/om901063aopenalex-snapshot
Synthesis of Pentafluorophenyl Silver by Means of Lewis Acid Catalysis: Structure of Silver Solvent Complexes
inferred← citeshttps://doi.org/10.1021/om970706aopenalex-snapshot
Synthesis and Reactivity of the Cationic Methylene Complex [Cp2ReCH2]+
inferred← citeshttps://doi.org/10.1021/om980401bopenalex-snapshot
Neutral and Cationic Tetracoordinated Aluminum Complexes Featuring Tridentate Nitrogen Donors: Synthesis, Structure, and Catalytic Activity for the Ring-Opening Polymerization of Propylene Oxide and ( d , l )-Lactide
inferred← citeshttps://doi.org/10.1021/om980783lopenalex-snapshot
Contributions to the Enantioselective Heck Reaction Using MeO−Biphep Ligands. The Case Against Dibenzylidene Acetone
inferred← citeshttps://doi.org/10.1021/om990892fopenalex-snapshot
Catalytic and Structural Studies on Complexes of a Binaphthyl−Phosphino−Oxazoline Auxiliary: The Meta Dialkyl Effect on Enantioselectivity
inferred← citeshttps://doi.org/10.1021/op050202lopenalex-snapshot
Stereoselective Process for a CCR3 Antagonist
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