On the public citation graph
The Use of Silyl Ketene Acetals and Enol Ethers in the Catalytic Enantioselective Alkylative Ring Opening of Oxa/Aza Bicyclic Alkenes
0 signed · 109 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/3527604693openalex-snapshot
Modern Rhodium‐Catalyzed Organic Reactions
inferredcites →https://doi.org/10.1002/ange.201106587openalex-snapshot
Enantioselective Total Synthesis of (−)‐Stenine
inferredcites →https://doi.org/10.1002/anie.201106587openalex-snapshot
Enantioselective Total Synthesis of (−)‐Stenine
inferredcites →https://doi.org/10.1016/s0040-4039(00)85255-7openalex-snapshot
The first example of aldol reactions between trimethylsilyl enol ethers and aldehydes by the aid of rhodium complex
inferredcites →https://doi.org/10.1021/ar00114a004openalex-snapshot
Reactive enolates from enol silyl ethers
inferredcites →https://doi.org/10.1021/ar010112aopenalex-snapshot
Transition Metal-Catalyzed Enantioselective Ring-Opening Reactions of Oxabicyclic Alkenes
inferredcites →https://doi.org/10.1021/cr020007uopenalex-snapshot
Rhodium-Catalyzed Carbon−Carbon Bond Forming Reactions of Organometallic Compounds
inferredcites →https://doi.org/10.1021/cr020022zopenalex-snapshot
Rhodium-Catalyzed Asymmetric 1,4-Addition and Its Related Asymmetric Reactions
inferredcites →https://doi.org/10.1021/ja00341a055openalex-snapshot
Synthesis of the cytotoxic germacranolide eucannabinolide
inferredcites →https://doi.org/10.1021/ja00459a039openalex-snapshot
Sesquiterpene lactones: total synthesis of (.+-.)-vernolepin and (.+-.)-vernomenin
inferredcites →https://doi.org/10.1021/ja00525a064openalex-snapshot
Synthesis of (.+-.)-linderalactone, (.+-.)-isolinderalactone, and (.+-.)-neolinderalactone
inferredcites →https://doi.org/10.1021/ja00540a029openalex-snapshot
Total synthesis of (.+-.)-isabelin
inferredcites →https://doi.org/10.1021/ja010262gopenalex-snapshot
Effects of Halide Ligands and Protic Additives on Enantioselectivity and Reactivity in Rhodium-Catalyzed Asymmetric Ring-Opening Reactions
inferredcites →https://doi.org/10.1021/ja031544eopenalex-snapshot
Palladium-Catalyzed Arylation of Trimethylsilyl Enolates of Esters and Imides. High Functional Group Tolerance and Stereoselective Synthesis of α-Aryl Carboxylic Acid Derivatives
inferredcites →https://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
inferredcites →https://doi.org/10.1021/ja036792popenalex-snapshot
Palladium-Catalyzed α-Arylation of Esters and Amides under More Neutral Conditions
inferredcites →https://doi.org/10.1021/ja037550sopenalex-snapshot
Scope of Palladium-Catalyzed Alkylative Ring Opening
inferredcites →https://doi.org/10.1021/ja0577701openalex-snapshot
Rhodium-Catalyzed Ring-Opening Reactions of N-Boc-Azabenzonorbornadienes with Amine Nucleophiles
inferredcites →https://doi.org/10.1021/ja993427iopenalex-snapshot
Palladium-Catalyzed Enantioselective Alkylative Ring Opening
inferredcites →https://doi.org/10.1021/jo9824605openalex-snapshot
Highly Enantioselective Hydrogenation of Cyclic Enamides Catalyzed by a Rh-PennPhos Catalyst
inferredcites →https://doi.org/10.1021/np060587gopenalex-snapshot
Unusual Naphthoquinone Derivatives from the Twigs of Avicennia marina
inferredcites →https://doi.org/10.1021/ol006052aopenalex-snapshot
Enantioselective Ring Opening of Aza and Oxabicyclic Alkenes with Dimethylzinc
inferredcites →https://doi.org/10.1021/ol0256062openalex-snapshot
Rhodium-Catalyzed Asymmetric Ring Opening of Oxabicyclic Alkenes with Organoboronic Acids
inferredcites →https://doi.org/10.1021/ol026220uopenalex-snapshot
Copper Phosphoramidite Catalyzed Enantioselective Ring-Opening of Oxabicyclic Alkenes: Remarkable Reversal of Stereocontrol
inferredcites →https://doi.org/10.1021/ol026579iopenalex-snapshot
An Expedient Enantioselective Route to Diaminotetralins: Application in the Preparation of Analgesic Compounds
inferredcites →https://doi.org/10.1021/ol900533hopenalex-snapshot
Optically Active Dinuclear Palladium Complexes Containing a Pd−Pd Bond: Preparation and Enantioinduction Ability in Asymmetric Ring-Opening Reactions
inferredcites →https://doi.org/10.1039/b902602aopenalex-snapshot
Rapid screening for asymmetric catalysts: the efficient connection of two different catalytic asymmetric reactions
inferredcites →https://doi.org/10.1039/c2cc16855copenalex-snapshot
Copper-catalyzed asymmetric ring opening of oxabicyclic alkenes with organolithium reagents
inferredcites →https://doi.org/10.1039/c3ob40430gopenalex-snapshot
Synthesis of a series of novel chiral Lewis base catalysts and their application in promoting asymmetric hydrosilylation of β-enamino esters
inferredcites →https://doi.org/10.1055/s-1983-30204openalex-snapshot
Silyl Enol Ethers in Synthesis - Part I
inferredcites →https://doi.org/10.1055/s-1983-30234openalex-snapshot
Silyl Enol Ethers in Synthesis - Part II
inferredcites →https://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
inferredcites →https://doi.org/10.1080/00304948809355878openalex-snapshot
SYNTHESIS AND REACTIONS OF FUNCTIONALIZED SILYLENOL ETHERS. A REVIEW
inferredcites →https://doi.org/10.1246/cl.1985.1535openalex-snapshot
TRITYL SALTS AS EFFICIENT CATALYSTS IN THE ALDOL REACTION
inferredcites →https://doi.org/10.1246/cl.1995.1129openalex-snapshot
Diels-Alder Reaction of 3-Methylthiofuran and Transformation of the Cycloadducts to Substituted Cyclohexenols
inferredcites →https://doi.org/10.1248/cpb.47.1579openalex-snapshot
Chemical Constituents of Glycosmis pentaphylla. Isolation of A Novel Naphthoquinone and A New Acridone Alkaloid.
inferredcites →https://doi.org/10.2174/092986709787002682openalex-snapshot
A Review on Hemisynthesis, Biosynthesis, Biological Activities, Mode of Action, and Structure-Activity Relationship of Podophyllotoxins: 2003- 2007
inferredcites →https://doi.org/10.2174/0929867305666220314204426openalex-snapshot
Podophyllotoxins: Current Status and Recent Developments
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4494476openalex-extracted
Rhodium-Catalyzed Ring-Opening Reactions of Azabicyclic Alkenes with Indole Nucleophiles
inferred← citeshttps://doi.org/10.1002/9781118941829.ch7openalex-snapshot
Nucleophilic Aliphatic Substitution
inferred← citeshttps://doi.org/10.1002/adsc.201701162openalex-snapshot
Cobalt‐Catalyzed Diastereoselective [4+2] Annulation of Phosphinamides with Heterobicyclic Alkenes at Room Temperature
inferred← citeshttps://doi.org/10.1002/adsc.201901152openalex-snapshot
Water‐Promoted Palladium‐Catalyzed Asymmetric Ring‐Opening of Oxabenzonorbornadienes with Alkoxysilanes
inferred← citeshttps://doi.org/10.1002/ajoc.201800251openalex-snapshot
Cobalt(III)‐Catalyzed [4+2] Annulation of Heterobicyclic Alkenes by sp2 C−H Activation
inferred← citeshttps://doi.org/10.1002/ajoc.201800569openalex-snapshot
Pd/Zn Co‐catalyzed Asymmetric Ring‐Opening Reactions of Aza/Oxabicyclic Alkenes with Oximes
inferred← citeshttps://doi.org/10.1002/ange.201506003openalex-snapshot
Cobalt‐Catalyzed Allylation of Heterobicyclic Alkenes: Ligand‐Induced Divergent Reactivities
inferred← citeshttps://doi.org/10.1002/ange.201600654openalex-snapshot
Exploiting Distal Reactivity of Coumarins: A Rhodium‐Catalyzed Vinylogous Asymmetric Ring‐Opening Reaction
inferred← citeshttps://doi.org/10.1002/ange.201604937openalex-snapshot
Rhodium‐Catalyzed Asymmetric Cycloisomerization and Parallel Kinetic Resolution of Racemic Oxabicycles
inferred← citeshttps://doi.org/10.1002/ange.201700632openalex-snapshot
Rhodium‐Catalyzed Enantioselective Isomerization of meso‐Oxabenzonorbornadienes to 1,2‐Naphthalene Oxides
inferred← citeshttps://doi.org/10.1002/ange.201704354openalex-snapshot
Iridium‐Catalyzed Enantioselective Allylic Substitution of Aliphatic Esters with Silyl Ketene Acetals as the Ester Enolates
inferred← citeshttps://doi.org/10.1002/ange.201811998openalex-snapshot
Rhodium(III)‐Catalyzed Enantioselective Coupling of Indoles and 7‐Azabenzonorbornadienes by C−H Activation/Desymmetrization
inferred← citeshttps://doi.org/10.1002/ange.201909596openalex-snapshot
Rhodium(I)/Zn(OTf)2‐Catalyzed Asymmetric Ring Opening/Cyclopropanation of Oxabenzonorbornadienes with Phosphorus Ylides
inferred← citeshttps://doi.org/10.1002/ange.202315092openalex-snapshot
Enantioselective Palladium(II)‐Catalyzed Desymmetrizative Coupling of 7‐Azabenzonorbornadienes with Alkynylanilines
inferred← citeshttps://doi.org/10.1002/anie.201506003openalex-snapshot
Cobalt‐Catalyzed Allylation of Heterobicyclic Alkenes: Ligand‐Induced Divergent Reactivities
inferred← citeshttps://doi.org/10.1002/anie.201600654openalex-snapshot
Exploiting Distal Reactivity of Coumarins: A Rhodium‐Catalyzed Vinylogous Asymmetric Ring‐Opening Reaction
inferred← citeshttps://doi.org/10.1002/anie.201604937openalex-snapshot
Rhodium‐Catalyzed Asymmetric Cycloisomerization and Parallel Kinetic Resolution of Racemic Oxabicycles
inferred← citeshttps://doi.org/10.1002/anie.201700632openalex-snapshot
Rhodium‐Catalyzed Enantioselective Isomerization of meso‐Oxabenzonorbornadienes to 1,2‐Naphthalene Oxides
inferred← citeshttps://doi.org/10.1002/anie.201704354openalex-snapshot
Iridium‐Catalyzed Enantioselective Allylic Substitution of Aliphatic Esters with Silyl Ketene Acetals as the Ester Enolates
inferred← citeshttps://doi.org/10.1002/anie.201811998openalex-snapshot
Rhodium(III)‐Catalyzed Enantioselective Coupling of Indoles and 7‐Azabenzonorbornadienes by C−H Activation/Desymmetrization
inferred← citeshttps://doi.org/10.1002/anie.201909596openalex-snapshot
Rhodium(I)/Zn(OTf)2‐Catalyzed Asymmetric Ring Opening/Cyclopropanation of Oxabenzonorbornadienes with Phosphorus Ylides
inferred← citeshttps://doi.org/10.1002/anie.202315092openalex-snapshot
Enantioselective Palladium(II)‐Catalyzed Desymmetrizative Coupling of 7‐Azabenzonorbornadienes with Alkynylanilines
inferred← citeshttps://doi.org/10.1002/asia.201801061openalex-snapshot
Desymmetrization of Achiral Heterobicyclic Alkenes through Catalytic Asymmetric Hydrophosphination
inferred← citeshttps://doi.org/10.1002/chem.201502718openalex-snapshot
Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth‐Generation Rhodium Catalytic System
inferred← citeshttps://doi.org/10.1002/chin.201448095openalex-snapshot
ChemInform Abstract: The Use of Silyl Ketene Acetals and Enol Ethers in the Catalytic Enantioselective Alkylative Ring Opening of Oxa/Aza Bicyclic Alkenes.
inferred← citeshttps://doi.org/10.1002/cjoc.201700596openalex-snapshot
Rh/Lewis Acid Catalyzed Regio‐, Diastereo‐ and Enantioselective Addition of 2‐Acyl Imidazoles with Allenes
inferred← citeshttps://doi.org/10.1002/ejoc.201800503openalex-snapshot
Palladium/Lewis Acid Cocatalyzed Reductive Asymmetric Ring‐Opening Reaction of Azabenzonorbornadienes with Tertiary Amines as the Hydrogen Source
inferred← citeshttps://doi.org/10.1007/3418_2015_165openalex-snapshot
Asymmetric Allylic Substitutions Using Organometallic Reagents
inferred← citeshttps://doi.org/10.1016/j.gresc.2026.01.003openalex-snapshot
Cobalt-catalyzed enantioselective hydroalkylation of oxanorbornene for the construction of chiral bridged oxabicyclic structures
inferred← citeshttps://doi.org/10.1016/j.tet.2016.05.031openalex-snapshot
An easy access to fused chromanones via rhodium catalyzed oxidative coupling of salicylaldehydes with heterobicyclic olefins
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.10.017openalex-snapshot
Iridium-catalyzed highly enantioselective ring opening reaction of oxabenzonorbornadienes with amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154685openalex-snapshot
Rhodium-catalyzed ring-opening reactions of heterobicyclic alkenes with heteroarene nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02437openalex-snapshot
Rhodium-Catalyzed Enantioselective Ring-Openings of Oxabicyclic Alkenes with Azole Nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00667openalex-snapshot
Palladium-Catalyzed syn-Stereocontrolled Ring-Opening of Oxabicyclic Alkenes with Sodium Arylsulfinates
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02117openalex-snapshot
Intramolecular Diels–Alder Reactions of Tethered Enoate Substituted Furans Induced by Dialkylaluminum Chloride
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01396openalex-snapshot
Water-Promoted Ir-Catalyzed Ring-Opening of Oxa(aza)benzonorbornadienes with Fluoroalkylamines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01957openalex-snapshot
Palladium-Catalyzed syn-Stereocontrolled Ring Opening of Oxabicyclic Alkenes with Arylsulfonyl Hydrazides
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00017openalex-snapshot
Iridium/Zinc-Co-Catalyzed Ring-Opening Reactions of Oxabicyclic Alkenes with Indole Nucleophiles: A Combined Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00765openalex-snapshot
Directing-Group-Controlled Ring-Opening Addition and Hydroarylation of Oxa/azabenzonorbornadienes with Arenes via C–H Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02829openalex-snapshot
Asymmetric Synthesis of 1,2-Dihydronaphthalene-1-ols via Copper-Catalyzed Intramolecular Reductive Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00851openalex-snapshot
Three-Component 1,2-Carboamidation of Bridged Bicyclic Alkenes via RhIII-Catalyzed Addition of C–H Bonds and Amidating Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04414openalex-snapshot
Palladium(II)-Catalyzed Enantioselective Ring Opening of Oxabenzonorbornadienes via Domino Aminopalladation of Alkynylanilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00971openalex-snapshot
Asymmetric Multi-Atom Insertion of Esters via Rh-Catalyzed Ring Opening of Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02110openalex-snapshot
Camphor-Based NHC Ligands with a Sulfur Ligator Atom in Rhodium Catalysis: Catalytic Advances in the Asymmetric Ring Opening of N-Protected Azabenzonorbornenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02300openalex-snapshot
Palladium/Lewis Acid Co-catalyzed Divergent Asymmetric Ring-Opening Reactions of Azabenzonorbornadienes with Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02452openalex-snapshot
Copper-Catalyzed Diastereoselective 1,2-Difunctionalization of Oxabenzonorbornadienes Leading to β-Thiocyanato Thioethers
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03226openalex-snapshot
Rhodium(III)-Catalyzed Chemo-divergent Couplings of Sulfoxonium Ylides with Oxa/azabicyclic Olefins
inferred← citeshttps://doi.org/10.1021/acscatal.4c02656openalex-snapshot
Copper-Catalyzed Dearomative trans-1,2-Carboamination
inferred← citeshttps://doi.org/10.1021/acscatal.5b00258openalex-snapshot
Ruthenium-Catalyzed Hydroarylations of Oxa- and Azabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.9b00655openalex-snapshot
Cobalt-Catalyzed Enantioselective and Chemodivergent Addition of Cyclopropanols to Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.9b02458openalex-snapshot
Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.2c12648openalex-snapshot
Diastereodivergent Desymmetric Annulation to Access Spirooxindoles: Chemical Probes for Mitosis
inferred← citeshttps://doi.org/10.1021/jacs.5c13397openalex-snapshot
Cobalt-Catalyzed Enantioselective Hydroalkylation of Oxa- or Azabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.8b01726openalex-snapshot
Nickel-Catalyzed Dearomative trans -1,2-Carboamination
inferred← citeshttps://doi.org/10.1038/s41467-025-67390-4openalex-snapshot
Concise synthesis of chiral tricyclic γ-lactams via synergistic isothiourea/Ir catalyzed asymmetric [3 + 2] annulation
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/c7qo00420fopenalex-snapshot
Platinum-catalyzed syn-stereocontrolled ring-opening of oxabicyclic alkenes with sodium arylsulfinates
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/c8ob02864hopenalex-snapshot
Nickel-catalyzed syn -stereocontrolled ring-opening of oxa- and azabicyclic alkenes with dialkylzinc reagents
inferred← citeshttps://doi.org/10.1039/c9cc00948eopenalex-snapshot
One-pot synthesis of benzo[ b ]fluorenones via a cobalt-catalyzed MHP-directed [3+2] annulation/ring-opening/dehydration sequence
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/d0cs00702aopenalex-snapshot
Catalytic asymmetric transformations of oxa- and azabicyclic alkenes
inferred← citeshttps://doi.org/10.1039/d0ob00659aopenalex-snapshot
Copper-catalyzed diastereoselective hydrothioetherification of oxa(aza)benzonorbornadienes
inferred← citeshttps://doi.org/10.1039/d1cc02387jopenalex-snapshot
Iron-catalysed enantioselective carbometalation of azabicycloalkenes
inferred← citeshttps://doi.org/10.1039/d5qo00118hopenalex-snapshot
Palladium( ii )-catalyzed enantioselective desymmetrization ring opening of oxabicyclic alkenes with alkynylanilines: efficient access to enantioenriched functionalized cyclohexenes
inferred← citeshttps://doi.org/10.1039/d6sc01491gopenalex-snapshot
Highly Cα-regio-, enantio- and diastereoselective Mukaiyama-type annulation of siloxyfurans: stereodivergent synthesis of multi-stereogenic tricyclic γ-lactones
inferred← citeshttps://doi.org/10.1055/a-2152-0355openalex-snapshot
Cobalt-Catalyzed Enantioselective Alkynylation of Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1055/s-0037-1611784openalex-snapshot
Rhodium-Catalyzed Allylation Reactions
inferred← citeshttps://doi.org/10.1139/cjc-2023-0225openalex-snapshot
Rhodium-catalyzed ring-opening reactions of heterobicyclic akenes with heteroarene nucleophiles: an experimental and computational investigation
inferred← citeshttps://doi.org/10.3390/molecules201219748openalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Oxabenzonorbornadienes with N-Substituted Piperazine Nucleophiles
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.