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Rhodium-Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon−Heteroatom Bond Forming Process
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Stereoselective palladium(0)-mediated synthesis of 1,4-disaccharides
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Scope of the nickel catalyzed asymmetric reductive ring opening reaction. Synthesis of enantiomerically enriched cyclohexenols
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Rhodium and proton catalysed reactions of 7-oxanorbornadienes with methanol. A synthetic route to methoxycyclohexadienols.
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Stereochemistry of the [Rh(CO)2Cl]2-catalyzed reaction of 7-oxabicyclo[2.2.1]hepta-2,5-dienes with methanol
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Sertraline Hydrochloride
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A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration Reactions
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Alkoxides as nucleophiles in (.pi.-allyl)palladium chemistry. Synthetic and mechanistic studies
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A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes
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Enantiospecific Synthesis of Allylamines via the Regioselective Rhodium-Catalyzed Allylic Amination Reaction
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Palladium-Catalyzed Enantioselective Alkylative Ring Opening
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High Affinity and Selectivity on 5-HT1A Receptor of 1-Aryl-4-[(1-tetralin)alkyl]piperazines. 2
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Synthesis and Evaluation of 6,7-Dihydroxy-2,3,4,8,9,13b-hexahydro-1H-benzo[6,7]cyclohepta[1,2,3-ef][3]benzazepine, 6,7-Dihydroxy-1,2,3,4,8,12b-hexahydroanthr[10,4a,4-cd]azepine, and 10-(Aminomethyl)-9,10-dihydro-1,2-dihydroxyanthracene as Conformationally Restricted Analogs of .beta.-Phenyldopamine
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Synthetic Studies of the Angucycline Antibiotics. Stereocontrolled Assembly of the SF 2315B Ring System
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Ring Opening Reactions of Oxabicyclic Compounds as a Route to Cyclic and Acyclic Compounds with Multiple Stereocenters
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Palladium-catalyzed Exchange of Allylic Groups of Ethers and Esters with Active Hydrogen Compounds. II.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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1,4-Dihydro-1,4-epoxynaphthalene
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ChemInform Abstract: Rhodium‐Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon—Heteroatom Bond Forming Process.
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inferred← citeshttps://doi.org/10.1016/j.cclet.2006.12.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gresc.2026.01.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.11.023openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.02.039openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.032openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2020.131739openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.10.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.11.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.03.137openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.07.070openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.089openalex-snapshot
Asymmetric ring opening reaction of oxabenzonorbornadienes with amines promoted by iridium/NMDPP complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154685openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0010-8545(02)00122-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00351-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01914-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.5c02582openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.7b00178openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.9b02582openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00017openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00593openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04816openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02300openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja034845xopenalex-snapshot
Rhodium-Catalyzed Asymmetric Ring Opening Reactions of Oxabicyclic Alkenes: Application of Halide Effects in the Development of a General Process
inferred← citeshttps://doi.org/10.1021/ja0577701openalex-snapshot
Rhodium-Catalyzed Ring-Opening Reactions of N-Boc-Azabenzonorbornadienes with Amine Nucleophiles
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Sequential Ru−Pd Catalysis: A Two-Catalyst One-Pot Protocol for the Synthesis of N- and O-Heterocycles
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Rhodium-Catalyzed Asymmetric Cyclodimerization of Oxa- and Azabicyclic Alkenes
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Diastereodivergent Desymmetric Annulation to Access Spirooxindoles: Chemical Probes for Mitosis
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Palladium-Catalyzed Cyclization Reactions of 2-Vinylthiiranes with Heterocumulenes. Regioselective and Enantioselective Formation of Thiazolidine, Oxathiolane, and Dithiolane Derivatives
inferred← citeshttps://doi.org/10.1021/jo025822oopenalex-snapshot
Remote Electronic Effects in the Rhodium-Catalyzed Nucleophilic Ring Opening of Oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.1021/jo048721uopenalex-snapshot
Nickel-Catalyzed Addition of Alkenylzirconium Reagents to Bicyclic Olefins: A Highly Regio- and Stereoselective Ring-Opening Reaction
inferred← citeshttps://doi.org/10.1021/jo051660vopenalex-snapshot
A Highly Regio- and Stereoselective Nickel-Catalyzed Ring-Opening Reaction of Alkyl- and Allylzirconium Reagents to 7-Oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.1021/jo060238ropenalex-snapshot
Rhodium(I)-Catalyzed Nucleophilic Ring-Opening Reactions of Oxabicyclo Adducts Derived from the [4 + 2]-Cycloaddition of 2-Imido-Substituted Furans
inferred← citeshttps://doi.org/10.1021/jo061269popenalex-snapshot
Synthesis of the Tetracyclic Framework of the Erythrina Alkaloids Using a [4 + 2]-Cycloaddition/Rh(I)-Catalyzed Cascade of 2-Imidofurans
inferred← citeshttps://doi.org/10.1021/jo201781xopenalex-snapshot
Diastereoselective Friedel–Crafts Alkylation of Hydronaphthalenes
inferred← citeshttps://doi.org/10.1021/jo3018507openalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Oxabenzonorbornadienes with Phenols
inferred← citeshttps://doi.org/10.1021/jo901248wopenalex-snapshot
Rhodium-Catalyzed Ring-Opening Reactions of a 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/ol0060782openalex-snapshot
Rhodium-Catalyzed Ring Opening of Vinyl Epoxides with Alcohols and Aromatic Amines
inferred← citeshttps://doi.org/10.1021/ol0069204openalex-snapshot
Synthesis of Biaryls via Unusual Deoxygenative Dimerization of 1,4-Epoxy-1,4-dihydroarenes Catalyzed by Palladium Complexes
inferred← citeshttps://doi.org/10.1021/ol025731dopenalex-snapshot
Highly Stereoselective Ring-Opening Addition of Terminal Acetylenes to Bicyclic Olefins Catalyzed by Nickel Complexes
inferred← citeshttps://doi.org/10.1021/ol026220uopenalex-snapshot
Copper Phosphoramidite Catalyzed Enantioselective Ring-Opening of Oxabicyclic Alkenes: Remarkable Reversal of Stereocontrol
inferred← citeshttps://doi.org/10.1021/ol026579iopenalex-snapshot
An Expedient Enantioselective Route to Diaminotetralins: Application in the Preparation of Analgesic Compounds
inferred← citeshttps://doi.org/10.1021/ol027104uopenalex-snapshot
A Mild and Efficient Method for the Stereoselective Formation of C−O Bonds: Palladium-Catalyzed Allylic Etherification Using Zinc(II) Alkoxides
inferred← citeshttps://doi.org/10.1021/ol034251zopenalex-snapshot
Asymmetric Reductive Ring-Opening of Bicyclic Olefins Catalyzed by Palladium and Nickel Complexes
inferred← citeshttps://doi.org/10.1021/ol049348fopenalex-snapshot
Rh(I)-Catalyzed Ring Opening of an IMDAF-Derived Oxabicyclo Cycloadduct as the Key Step in the Synthesis of (±)-epi-Zephyranthine
inferred← citeshttps://doi.org/10.1021/ol0527330openalex-snapshot
Synthesis of the Erythrina Alkaloid 3-Demethoxyerythratidinone. Novel Acid-Induced Rearrangements of Its Precursors
inferred← citeshttps://doi.org/10.1021/ol2008236openalex-snapshot
Diastereoselective Intramolecular Friedel–Crafts Alkylation of Tetralins
inferred← citeshttps://doi.org/10.1021/ol4000668openalex-snapshot
Expedient Synthesis of Chiral Oxazolidinone Scaffolds via Rhodium-Catalyzed Asymmetric Ring-Opening with Sodium Cyanate
inferred← citeshttps://doi.org/10.1021/ol4009393openalex-snapshot
Metal–Ligand Binding Affinity vs Reactivity: Qualitative Studies in Rh(I)-Catalyzed Asymmetric Ring-Opening Reactions
inferred← citeshttps://doi.org/10.1021/ol5003219openalex-snapshot
Copper-Catalyzed Enantioselective Formal Hydroamination of Oxa- and Azabicyclic Alkenes with Hydrosilanes and Hydroxylamines
inferred← citeshttps://doi.org/10.1021/ol801549topenalex-snapshot
Rhodium-Catalyzed Asymmetric Ring-Opening Alkynylation of Azabenzonorbornadienes
inferred← citeshttps://doi.org/10.1021/ol902685hopenalex-snapshot
Construction of All-Carbon Quaternary Center by R2AlCl−Mediated Ring-Opening Reaction of Oxacycles
inferred← citeshttps://doi.org/10.1021/om3000295openalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Azabicyclic Alkenes with Phenols
inferred← citeshttps://doi.org/10.1023/a:1013832630565openalex-snapshot
Solvias Josiphos Ligands: From Discovery to Technical Applications
inferred← citeshttps://doi.org/10.1038/s41557-022-01110-zopenalex-snapshot
A synergistic Rh(I)/organoboron-catalysed site-selective carbohydrate functionalization that involves multiple stereocontrol
inferred← citeshttps://doi.org/10.1038/srep40491openalex-snapshot
Mechanism, reactivity, and regioselectivity in rhodium-catalyzed asymmetric ring-opening reactions of oxabicyclic alkenes: a DFT Investigation
inferred← citeshttps://doi.org/10.1039/b108808dopenalex-snapshot
Rhodium-catalysed addition of arylboronic acids to oxabenzonorbornadienesElectronic supplementary information (ESI) available: experimental data. See http://www.rsc.org/suppdata/cc/b1/b108808d/
inferred← citeshttps://doi.org/10.1039/b316819kopenalex-snapshot
The syntheses and catalytic applications of unsymmetrical ferrocene ligands
inferred← citeshttps://doi.org/10.1039/c2cc31880fopenalex-snapshot
Cobalt-catalyzed asymmetric addition of silylacetylenes to oxa- and azabenzonorbornadienes
inferred← citeshttps://doi.org/10.1039/c2ob26775fopenalex-snapshot
Iridium-catalyzed asymmetric hydroalkynylation reactions of oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.1039/c3ob40891dopenalex-snapshot
Iridium-catalyzed asymmetric ring-opening of azabicyclic alkenes with alcohols
inferred← citeshttps://doi.org/10.1039/c3ob42199fopenalex-snapshot
Platinum-catalyzed anti-stereocontrolled ring-opening of oxabicyclic alkenes with Grignard reagents
inferred← citeshttps://doi.org/10.1039/c5ob02331aopenalex-snapshot
Rhodium-catalyzed asymmetric ring opening reaction of oxabenzonorbornadienes with amines using ZnI 2 as the activator
inferred← citeshttps://doi.org/10.1039/c7qo01064hopenalex-snapshot
Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides
inferred← citeshttps://doi.org/10.1039/c7qo01163fopenalex-snapshot
Asymmetric ring-opening reactions of azabenzonorbornadienes through transfer hydrogenation using secondary amines as hydrogen sources: tuning of absolute configuration by acids
inferred← citeshttps://doi.org/10.1039/c8qo01403eopenalex-snapshot
Ir-Catalyzed ring-opening of oxa(aza)benzonorbornadienes with water or alcohols
inferred← citeshttps://doi.org/10.1039/c9qo00041kopenalex-snapshot
Palladium/silver co-catalyzed syn -stereoselective asymmetric ring-opening reactions of azabenzonorbornadienes with amides
inferred← citeshttps://doi.org/10.1039/d0cc03158eopenalex-snapshot
Enantioselective synthesis of indole derivatives by Rh/Pd relay catalysis and their anti-inflammatory evaluation
inferred← citeshttps://doi.org/10.1039/d0cs00702aopenalex-snapshot
Catalytic asymmetric transformations of oxa- and azabicyclic alkenes
inferred← citeshttps://doi.org/10.1039/d3cc00604bopenalex-snapshot
Palladium-catalyzed stereocontrolled ring-opening of 7-oxabenzonorbornadienes with organic carboxylic acids
inferred← citeshttps://doi.org/10.1055/s-0037-1611784openalex-snapshot
Rhodium-Catalyzed Allylation Reactions
inferred← citeshttps://doi.org/10.1073/pnas.0307271101openalex-snapshot
Rhodium-catalyzed asymmetric ring opening reactions of oxabicyclic alkenes: Catalyst and substrate studies leading to a mechanistic working model
inferred← citeshttps://doi.org/10.1080/00397911.2011.626140openalex-snapshot
Ruthenium-Catalyzed Nucleophilic Ring-Opening Reactions of 7-Oxabenzonorbornadienes with Methanol
inferred← citeshttps://doi.org/10.1107/s1600536802021608openalex-snapshot
(1R*,2R*)-2-(Methylphenylamino)-1,2-dihydronaphthalen-1-ol–water (4/1)
inferred← citeshttps://doi.org/10.1139/cjc-2018-0459openalex-snapshot
Oxidative ring-opening of benzothiazole derivatives
inferred← citeshttps://doi.org/10.2174/1570179416666181122094643openalex-snapshot
Recent Advances in Transition Metal-Catalyzed Reactions of Oxabenzonorbornadiene
inferred← citeshttps://doi.org/10.3184/030823402103172491openalex-snapshot
Syntheses of and Photochemical Studies of 2,3-disubstituted 1,4-epoxy-1,4-dihydronaphthalenes
inferred← citeshttps://doi.org/10.3184/030823408x287104openalex-snapshot
Regio- and stereospecific synthesis of a new benzoconduritol-C derivative
inferred← citeshttps://doi.org/10.3184/174751913x13663103976700openalex-snapshot
Rhodium-catalysed Nucleophilic Ring Opening Reaction of 1- and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines
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