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The Complete Characterization of a Rhodium Lewis Acid−Dipolarophile Complex as an Intermediate for the Enantioselective Catalytic 1,3-Dipolar Cycloaddition of C,N-Diphenylnitrone to Methacrolein

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inferredcites →https://doi.org/10.1002/(sici)1521-3773(19990503)38:9<1219::aid-anie1219>3.0.co;2-dopenalex-snapshot
A Stable and Recoverable Chiral Ru Lewis Acid: Synthesis, Asymmetric Diels–Alder Catalysis and Structure of the Lewis Acid Methacrolein Complex
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19990503)38:9<1223::aid-anie1223>3.0.co;2-aopenalex-snapshot
Synthesis and Biological Evaluation of a Cyclo--tetrapeptide as a Somatostatin Analogue
inferredcites →https://doi.org/10.1002/3527600256openalex-snapshot
Cycloaddition Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.199507981openalex-snapshot
C2‐Symmetric Cationic Copper( II ) Complexes as Chiral Lewis Acids: Counterion Effects in the Enantioselective Diels–Alder Reaction
inferredcites →https://doi.org/10.1021/cr970324eopenalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition Reactions
inferredcites →https://doi.org/10.1021/ja017814fopenalex-snapshot
Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4868679openalex-extracted
Enantioselective Friedel-Crafts Alkylation of 1,3,5-Trimethoxybenzene with Trans-Β-Nitrostyrenes Catalysed by [Cp*Rh{(R)-Prophos}(H2o)][Sbf6]2 (Prophos = Propane-1,2-Diyl-Bis(Diphenylphosphane)
inferred← citeshttps://doi.org/10.1002/adsc.200700010openalex-snapshot
Asymmetric 1,3‐Dipolar Cycloaddition Reaction between α,β‐Unsaturated Aldehydes and Nitrones Catalyzed by Well‐Defined Iridium or Rhodium Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.201501099openalex-snapshot
Oxidative Coupling of Enamines and Disulfides via Tetrabutylammonium Iodide/ tert‐ Butyl Hydroperoxide‐Mediated Intermolecular Oxidative C( sp 2 )S Bond Formation Under Transition Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ange.200502308openalex-snapshot
Lewis Acid Catalyzed Asymmetric Cycloadditions of Nitrones: α′‐Hydroxy Enones as Efficient Reaction Partners
inferred← citeshttps://doi.org/10.1002/ange.200704618openalex-snapshot
Cationic Chiral Dirhodium Carboxamidates Are Activated for Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201201787openalex-snapshot
Katalytische selektive Synthese
inferred← citeshttps://doi.org/10.1002/anie.200502308openalex-snapshot
Lewis Acid Catalyzed Asymmetric Cycloadditions of Nitrones: α′‐Hydroxy Enones as Efficient Reaction Partners
inferred← citeshttps://doi.org/10.1002/anie.200704618openalex-snapshot
Cationic Chiral Dirhodium Carboxamidates Are Activated for Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201201787openalex-snapshot
Catalytic Selective Synthesis
inferred← citeshttps://doi.org/10.1002/asia.200700344openalex-snapshot
Asymmetric 1,3‐Dipolar Cycloadditions of N‐Benzyl and N‐Diphenylmethyl Nitrones and α,β‐Unsaturated Aldehydes Catalyzed by Bis‐Titanium Chiral Lewis Acids
inferred← citeshttps://doi.org/10.1002/asia.200800063openalex-snapshot
Iron‐ and Ruthenium‐Lewis Acid Catalyzed Asymmetric 1,3‐Dipolar Cycloaddition Reactions between Enals and Diaryl Nitrones
inferred← citeshttps://doi.org/10.1002/cctc.201505050openalex-snapshot
In Honour of the 70th Birthday of Professor Luis A. Oro
inferred← citeshttps://doi.org/10.1002/chem.200701140openalex-snapshot
Half‐Sandwich Rhodium (and Iridium) Complexes as Enantioselective Catalysts for the 1,3‐Dipolar Cycloaddition of 3,4‐Dihydroisoquinoline N‐Oxide to Methacrylonitrile
inferred← citeshttps://doi.org/10.1002/chem.201100053openalex-snapshot
Catalytic Asymmetric 1,3‐Dipolar Cycloaddition of Nitrones to Alkylidene Malonates: Highly Enantioselective Synthesis of Multisubstituted Isoxazolidines
inferred← citeshttps://doi.org/10.1002/chem.201601301openalex-snapshot
Temperature Dual Enantioselective Control in a Rhodium‐Catalyzed Michael‐Type Friedel–Crafts Reaction: A Mechanistic Explanation
inferred← citeshttps://doi.org/10.1002/chem.201702330openalex-snapshot
α,β‐Unsaturated Amides as Dipolarophiles: Catalytic Asymmetric exo‐Selective 1,3‐Dipolar Cycloaddition with Nitrones
inferred← citeshttps://doi.org/10.1002/ejic.200600408openalex-snapshot
Chiral Half‐Sandwich Ruthenium(II) Complexes as Catalysts in 1,3‐Dipolar Cycloaddition Reactions of Nitrones with Methacrolein
inferred← citeshttps://doi.org/10.1002/jhet.682openalex-snapshot
Reaction of N‐(phenyl and methyl)‐C‐arylnitrones with DMAD in ionic liquid: Efficient synthesis of Δ4‐isoxazolines
inferred← citeshttps://doi.org/10.1007/3418_2015_141openalex-snapshot
The Future of Catalysis by Chiral Lewis Acids
inferred← citeshttps://doi.org/10.1007/7081_2009_1openalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition Reactions Catalyzed by Heterocycle-Based Metal Complexes
inferred← citeshttps://doi.org/10.1007/978-3-642-15334-1_8openalex-snapshot
Iridium-Catalyzed 1,3-Dipolar Cycloadditions
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00428-6openalex-snapshot
4.22 Intermolecular 1,3-Dipolar Cycloadditions of Alkenes, Alkynes, and Allenes
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00011-xopenalex-snapshot
Five-Membered Ring Systems with O & N Atoms
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00039-1openalex-snapshot
(3 + 2) Cycloaddition of 1,3-Dipoles
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.09.003openalex-snapshot
Synthesis and structure of chiral-at-metal complexes with the ligand (S)-2-[(Sp)-2-(diphenylphosphino)ferrocenyl]-4-isopropyloxazoline
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.10.029openalex-snapshot
Palladacycle mediated synthesis of cyano-functionalized chiral 1,2-diphosphine and subsequent functional group transformations
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123377openalex-snapshot
Enantioselective Friedel-Crafts alkylation of 1,3,5-trimethoxybenzene with trans-β-nitrostyrenes catalysed by [Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane)
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.02.030openalex-snapshot
Chiral-at-metal ruthenium(II) complexes as catalysts in the asymmetric cyclopropanation reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.01.021openalex-snapshot
Enantioselective catalysts based on the chiral fragment (η5-C5Me5)Ir(Prophos) for Diels–Alder reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.028openalex-snapshot
Asymmetric cycloaddition reactions between 2-benzopyrylium-4-olates and 3-(2-alkenoyl)-2-oxazolidinones in the presence of 2,6-bis(oxazolinyl)pyridine-lanthanoid complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.076openalex-snapshot
Investigations of regio- and stereoselectivities in the synthesis of cytotoxic isoxazolidines through 1,3-dipolar cycloadditions of nitrones to dipolarophiles bearing an allylic oxygen
inferred← citeshttps://doi.org/10.1016/j.tet.2007.01.009openalex-snapshot
Asymmetric 1,3-dipolar cycloadditions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.03.130openalex-snapshot
CuI–Fesulphos complexes: efficient chiral catalysts for asymmetric 1,3-dipolar cycloaddition of azomethine ylides
inferred← citeshttps://doi.org/10.1016/j.tet.2007.06.033openalex-snapshot
Chiral ruthenium Lewis acid-catalyzed nitrile oxide cycloadditions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.110openalex-snapshot
Hydrazide-catalyzed 1,3-dipolar nitrone cycloadditions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.11.109openalex-snapshot
Chiral bis(2-oxazolinyl)xanthene (xabox)/transition-metal complexes catalyzed 1,3-dipolar cycloaddition reactions and Diels–Alder reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2013.08.084openalex-snapshot
Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2-ones
inferred← citeshttps://doi.org/10.1016/j.tet.2017.03.024openalex-snapshot
Synthesis of spiroisoxazolidinyl-benzoisothiazolines by 1,3-dipolar cycloaddition of benzoisothiazole-2,2-dioxide-3-ylidenes with nitrones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.11.005openalex-snapshot
Asymmetric reduction of racemic 2-isoxazolines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.04.002openalex-snapshot
Asymmetric 1,3-dipolar cycloaddition reaction of α,β-unsaturated nitriles with nitrones catalyzed by chiral-at-metal rhodium or iridium complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.05.003openalex-snapshot
Enantioselective Friedel–Crafts alkylations catalysed by well-defined iridium and rhodium half-sandwich complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.04.006openalex-snapshot
Asymmetric 1,3-dipolar cycloaddition reactions between methacrylonitrile and nitrones catalysed by well-defined M(diphosphane) (M = Rh, Ir) complexes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.03.151openalex-snapshot
Improved catalysis of nitrone 1,3-dipolar cycloadditions by solving the aggregation issue of the DBFOX/Ph-transition metal complexes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.05.176openalex-snapshot
A simple one-pot, three-component, catalytic, highly enantioselective isoxazolidine synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.076openalex-snapshot
One-pot synthesis of vinylisoxazolidines from simple hydroxylamines and conjugated carbonyls
inferred← citeshttps://doi.org/10.1016/s0959-6380(05)80333-2openalex-snapshot
Five-membered ring systems: with O & N atoms
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00543openalex-snapshot
Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry
inferred← citeshttps://doi.org/10.1021/acsomega.0c03485openalex-snapshot
Catalytic Enantioselective Alkylation of Indoles with trans -4-Methylthio-β-Nitrostyrene
inferred← citeshttps://doi.org/10.1021/cr5007182openalex-snapshot
Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions
inferred← citeshttps://doi.org/10.1021/ic301866yopenalex-snapshot
A Palladium(II) Center Activates Nitrile Ligands toward 1,3-Dipolar Cycloaddition of Nitrones Substantially More than the Corresponding Platinum(II) Center
inferred← citeshttps://doi.org/10.1021/ic9015993openalex-snapshot
Reactions of a Phosphinoaldehyde with PdII, RhI, and IrIPrecursors, Including the Formation of Complexes Containing a P,OH-Chelated Phosphinohemiacetal Ligand: a New Bonding Mode
inferred← citeshttps://doi.org/10.1021/ja0523284openalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition Reaction of Nitrones and Acrolein with a Bis-Titanium Catalyst as Chiral Lewis Acid
inferred← citeshttps://doi.org/10.1021/ja1081603openalex-snapshot
Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Propioloylpyrazoles and Acryloylpyrazoles Induced by Chiral π-Cation Catalysts
inferred← citeshttps://doi.org/10.1021/ja202676aopenalex-snapshot
Solvent Enhancement of Reaction Selectivity: A Unique Property of Cationic Chiral Dirhodium Carboxamidates
inferred← citeshttps://doi.org/10.1021/ja207664ropenalex-snapshot
Asymmeric Formal [3 + 3]-Cycloaddition Reactions of Nitrones with Electrophilic Vinylcarbene Intermediates
inferred← citeshttps://doi.org/10.1021/jacs.5c01753openalex-snapshot
Dynamic Kinetic Asymmetric Hydroacylation: Racemization by Soft Enolization
inferred← citeshttps://doi.org/10.1021/jo062200kopenalex-snapshot
Conformational Preferences of Methacrolein in Diels−Alder and 1,3-Dipolar Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1021/jo201061fopenalex-snapshot
Asymmetric Cycloaddition Reactions of Diazoesters with 2-Alkenoic Acid Derivatives Catalyzed by Binaphthyldiimine–Ni(II) complexes
inferred← citeshttps://doi.org/10.1021/jo5001737openalex-snapshot
Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C-Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational
inferred← citeshttps://doi.org/10.1021/jo5012625openalex-snapshot
Asymmetric Synthesis of Spiro[isoxazolin-3,3′-oxindoles] via the Catalytic 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxides
inferred← citeshttps://doi.org/10.1021/jo802392copenalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides Catalyzed by Chiral Binaphthyldiimine-Ni(II) Complexes
inferred← citeshttps://doi.org/10.1021/ol5026525openalex-snapshot
Direct Oxidative Coupling of Enamines and Electron-Deficient Amines: TBAI/TBHP-Mediated Synthesis of Substituted Diaminoalkenes under Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/ol702123nopenalex-snapshot
Asymmetric 1,3-Dipolar Cycloadditions of Nitrones and Methacrolein Catalyzed by Chiral Bis-Titanium Lewis Acid: A Dramatic Effect of N-Substituent on Nitrone
inferred← citeshttps://doi.org/10.1021/om049559oopenalex-snapshot
Toward an Understanding of the Anion Effect in CpRu-Based Diels−Alder Catalysts via PGSE-NMR Measurements
inferred← citeshttps://doi.org/10.1021/om050973dopenalex-snapshot
Chiral Phosphinooxazoline−Ruthenium(II) and −Osmium(II) Complexes as Catalysts in Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/om200859zopenalex-snapshot
Enantioselective Catalysts for the Diels–Alder Reaction between Methacrolein and Cyclopentadiene Based on the Chiral Fragment (η5-C5Me5)M(chiral diphosphane) (M = Rh, Ir)
inferred← citeshttps://doi.org/10.1021/om301089copenalex-snapshot
Chiral Octahedral Phosphano–Oxazoline Iridium(III) Complexes as Catalysts in Asymmetric Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1021/om700717eopenalex-snapshot
Complete Characterization of a Chiral Lewis Acid−Product Complex for the Enantioselective Diels−Alder Reaction between Methacrolein and Cyclopentadiene: Mechanistic Considerations
inferred← citeshttps://doi.org/10.1021/om8009188openalex-snapshot
Asymmetric Synthesis of Functionalized 1,2-Diphosphine via the Chemoselective Hydrophosphination of Coordinated Allylic Phosphines
inferred← citeshttps://doi.org/10.1039/b618720jopenalex-snapshot
Pentamethylcyclopentadienyl-iridium( iii ) complexes with pyridylamino ligands: synthesis and applications as asymmetric catalysts for Diels–Alder reactions
inferred← citeshttps://doi.org/10.1039/b804987dopenalex-snapshot
6,6′-Substituent effect of BINOL in bis-titanium chiral Lewis acid catalyzed 1,3-dipolar cycloaddition of nitrones
inferred← citeshttps://doi.org/10.1039/c0nj00150copenalex-snapshot
Intramolecular approach to some new D-ring-fused steroidal isoxazolidines by 1,3-dipolar cycloaddition: synthesis, theoretical and in vitro pharmacological studies
inferred← citeshttps://doi.org/10.1039/c1ob06144eopenalex-snapshot
Electronic effects in 1,3-dipolar cycloaddition reactions of N-alkyl and N-benzyl nitrones with dipolarophiles
inferred← citeshttps://doi.org/10.1039/c2ra21205fopenalex-snapshot
Enantiomerically pure compounds related to chiral hydroxy acids derived from renewable resources
inferred← citeshttps://doi.org/10.1039/c4cy01533aopenalex-snapshot
Asymmetric 1,3-dipolar cycloaddition reactions between enals and nitrones catalysed by half-sandwich rhodium or iridium diphosphane complexes
inferred← citeshttps://doi.org/10.1039/c8cs00872hopenalex-snapshot
Metal-catalyzed regiodivergent organic reactions
inferred← citeshttps://doi.org/10.1080/00397910903537349openalex-snapshot
Rapid, Highly Efficient, and Room-Temperature TiCl4-Catalyzed Synthesis of Δ4-Isoxazolines Under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1246/bcsj.79.1069openalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
inferred← citeshttps://doi.org/10.1351/pac200880051013openalex-snapshot
Asymmetric Lewis acid-catalyzed 1,3-dipolar cycloadditions
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