On the public citation graph

Rhodium-Catalyzed Asymmetric Ring Opening Reactions of Oxabicyclic Alkenes: Application of Halide Effects in the Development of a General Process

https://doi.org/10.1021/ja034845x
0 signed · 182 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20020104)41:1<26::aid-anie26>3.0.co;2-9openalex-snapshot
Halide Effects in Transition Metal Catalysis
inferredcites →https://doi.org/10.1002/ange.19951070711openalex-snapshot
C2‐Symmetrische, kationische Kupfer( II )‐Komplexe als chirale Lewis‐Säuren – Einfluß des Gegenions bei enantioselektiven Diels‐Alder‐Reaktionen
inferredcites →https://doi.org/10.1016/s0020-1693(00)89400-1openalex-snapshot
Solid-state isomerism and intermetallic interactions in rhodium(I) and carbonyl--amine complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)00904-9openalex-snapshot
Rhodium-catalysed asymmetric ring opening of oxabicyclic alkenes with heteroatom nucleophiles
inferredcites →https://doi.org/10.1016/s0040-4020(01)00351-9openalex-snapshot
Rhodium-catalysed asymmetric ring opening reactions with carboxylate nucleophiles
inferredcites →https://doi.org/10.1021/ja000134copenalex-snapshot
Rhodium-Catalyzed Asymmetric Alcoholysis and Aminolysis of Oxabenzonorbornadiene: A New Enantioselective Carbon−Heteroatom Bond Forming Process
inferredcites →https://doi.org/10.1021/ja00074a085openalex-snapshot
Catalytic ring-closing metathesis of functionalized dienes by a ruthenium carbene complex
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/ol005729ropenalex-snapshot
Rhodium-Catalyzed Asymmetric Ring Opening of Oxabicyclic Alkenes with Phenols
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/om9509599openalex-snapshot
Synthesis and Solution Structure of Palladium Tris(o-tolyl)phosphine Mono(amine) Complexes
inferredcites →https://doi.org/10.1021/om9509608openalex-snapshot
Halide and Amine Influence in the Equilibrium Formation of Palladium Tris(o-tolyl)phosphine Mono(amine) Complexes from Palladium Aryl Halide Dimers
inferredcites →https://doi.org/10.1039/a806324iopenalex-snapshot
Chloride ion effects on kinetic resolution in Pd-catalysed allylic alkylation
inferredcites →https://doi.org/10.1039/jr9570002445openalex-snapshot
477. The reaction of monoamines with chloro-bridged complexes of palladium(II)
inferredcites →https://doi.org/10.1055/s-1998-1664openalex-snapshot
On the Counterion Dependence of the Rhodium(I)-Catalysed [4 + 2] Cycloaddition - A Remarkable Accelerating Effect of the Hexafluoroantimonate Anion

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/10.1002/047084289x.rn00699openalex-snapshot
Chloro(1,5-cyclooctadiene)rhodium(I) Dimer
inferred← citeshttps://doi.org/10.1002/047084289x.rn00699.pub2openalex-snapshot
Chloro(1,5‐Cyclooctadiene)Rhodium(I) Dimer
inferred← citeshttps://doi.org/10.1002/9780470842898.rn00699openalex-snapshot
Chloro(1,5-cyclooctadiene)rhodium(I) Dimer
inferred← citeshttps://doi.org/10.1002/9781118662083.cot07-007openalex-snapshot
Formation of Alcohols and Phenols by Ether Cleavage
inferred← citeshttps://doi.org/10.1002/9783527630639.ch13openalex-snapshot
Catalytic Asymmetric Ring Opening: A Transfer from Academia to Industry
inferred← citeshttps://doi.org/10.1002/9783527633388.ch10openalex-snapshot
CarbonHeteroatom Bond Formation by RhI‐Catalyzed Ring‐Opening Reactions
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz09669openalex-snapshot
Lautens technology
inferred← citeshttps://doi.org/10.1002/adsc.201000236openalex-snapshot
Asymmetric Ring Opening of Benzo‐7‐oxabicyclo[2.2.1]heptadienes with Cationic Rhodium Complexes
inferred← citeshttps://doi.org/10.1002/adsc.201200771openalex-snapshot
Lewis Acid‐Catalyzed Ring‐Opening Functionalizations of 1,4‐Epoxy‐1,4‐dihydronaphthalenes
inferred← citeshttps://doi.org/10.1002/adsc.201600520openalex-snapshot
Enantioselective Ring Opening Reactions of Azabenzonorbornadienes with Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/ajoc.201300077openalex-snapshot
Iridium/NMDPP Catalyzed Asymmetric Ring‐Opening Reaction of Oxabenzonorbornadienes with Phenolic or Naphtholic Nucleophiles
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/ajoc.201900033openalex-snapshot
Radical Addition of Thiols to Oxa(aza)bicyclic Alkenes in Water
inferred← citeshttps://doi.org/10.1002/ange.200602482openalex-snapshot
Chirale Ferrocenliganden in der asymmetrischen Katalyse
inferred← citeshttps://doi.org/10.1002/ange.200902046openalex-snapshot
Nucleophilic Opening of Oxabicyclic Ring Systems
inferred← citeshttps://doi.org/10.1002/ange.201101773openalex-snapshot
Rhodium‐Catalyzed Domino Enantioselective Synthesis of Bicyclo[2.2.2]lactones
inferred← citeshttps://doi.org/10.1002/ange.201201636openalex-snapshot
Industrielle Anwendungen der Diels‐Alder‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.201303507openalex-snapshot
Rhodium(III)‐Catalyzed Coupling of Arenes with 7‐Oxa/Azabenzonorbornadienes by CH Activation
inferred← citeshttps://doi.org/10.1002/ange.201309126openalex-snapshot
Atom‐Economic, Regiodivergent, and Stereoselective Coupling of Imidazole Derivatives with Terminal Allenes
inferred← citeshttps://doi.org/10.1002/ange.201400218openalex-snapshot
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/ange.201405834openalex-snapshot
Highly Enantioselective Rhodium(I)‐Catalyzed Carbonyl Carboacylations Initiated by CC Bond Activation
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.201909596openalex-snapshot
Rhodium(I)/Zn(OTf)2‐Catalyzed Asymmetric Ring Opening/Cyclopropanation of Oxabenzonorbornadienes with Phosphorus Ylides
inferred← citeshttps://doi.org/10.1002/anie.200602482openalex-snapshot
Recent Applications of Chiral Ferrocene Ligands in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200902046openalex-snapshot
Nucleophilic Opening of Oxabicyclic Ring Systems
inferred← citeshttps://doi.org/10.1002/anie.201101773openalex-snapshot
Rhodium‐Catalyzed Domino Enantioselective Synthesis of Bicyclo[2.2.2]lactones
inferred← citeshttps://doi.org/10.1002/anie.201201636openalex-snapshot
Industrial Applications of the Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1002/anie.201303507openalex-snapshot
Rhodium(III)‐Catalyzed Coupling of Arenes with 7‐Oxa/Azabenzonorbornadienes by CH Activation
inferred← citeshttps://doi.org/10.1002/anie.201309126openalex-snapshot
Atom‐Economic, Regiodivergent, and Stereoselective Coupling of Imidazole Derivatives with Terminal Allenes
inferred← citeshttps://doi.org/10.1002/anie.201400218openalex-snapshot
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/anie.201405834openalex-snapshot
Highly Enantioselective Rhodium(I)‐Catalyzed Carbonyl Carboacylations Initiated by CC Bond Activation
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.201909596openalex-snapshot
Rhodium(I)/Zn(OTf)2‐Catalyzed Asymmetric Ring Opening/Cyclopropanation of Oxabenzonorbornadienes with Phosphorus Ylides
inferred← citeshttps://doi.org/10.1002/ardp.202100113openalex-snapshot
Synthesis and biological evaluation of some 1‐naphthol derivatives as antioxidants, acetylcholinesterase, and carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1002/chem.200800222openalex-snapshot
PGSE NMR Diffusion Overhauser Studies on [Ru(Cp*)(η6‐arene)][PF6], Plus a Variety of Transition‐Metal, Inorganic, and Organic Salts: An Overview of Ion Pairing in Dichloromethane
inferred← citeshttps://doi.org/10.1002/chem.201405558openalex-snapshot
Biaryl Synthesis by Ring‐Opening Friedel–Crafts Arylation of 1,4‐Epoxy‐1,4‐dihydronaphthalenes Catalyzed by Iron Trichloride
inferred← citeshttps://doi.org/10.1002/chem.201500816openalex-snapshot
Palladium/Zinc Co‐Catalyzed syn‐Stereoselectively Asymmetric Ring‐Opening Reaction of Oxabenzonorbornadienes with Phenols
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.200414032openalex-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/10.1002/cjoc.201090059openalex-snapshot
Rhodium‐catalyzed Asymmetric Ring‐opening Reactions of N‐Boc‐azabenzonorbornadiene with N‐Substituted Piperazine Nucleophiles
inferred← citeshttps://doi.org/10.1002/cjoc.201100679openalex-snapshot
A Facile Synthesis of Enantiomerically Pure (R)‐6‐Arylbinols
inferred← citeshttps://doi.org/10.1002/ejoc.200700772openalex-snapshot
Palladium‐Catalyzed 1,2‐Addition of Organic Halides and Terminal Alkynes to 7‐Oxabenzonorbornadiene: An Efficient Route to Polyaromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1002/ejoc.200800424openalex-snapshot
Alkynyl Halides in Ruthenium(II)‐Catalyzed [2+2] Cycloadditions of Bicyclic Alkenes
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/10.1002/ejoc.201801372openalex-snapshot
Palladium Catalyzed Tandem Reaction of Oxabenzonorbornadienes with Anhydrides
inferred← citeshttps://doi.org/10.1002/ejoc.202100093openalex-snapshot
A DFT Study on the Mechanism and Origin of Regioselectivity in the Rhodium/Diene‐Catalyzed Ring‐Opening Reactions of C1‐Substituted Oxabenzonorbornadienes with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.70745openalex-snapshot
Development of Sandwich‐Compound‐Based Planar‐Chiral Six‐Membered Unsaturated N ‐Heterocyclic Carbene Ligands
inferred← citeshttps://doi.org/10.1007/128_2009_12openalex-snapshot
Rhodium-Catalyzed C–H Bond Arylation of Arenes
inferred← citeshttps://doi.org/10.1007/3418_2011_15openalex-snapshot
Allylic Substitutions Catalyzed by Miscellaneous Metals
inferred← citeshttps://doi.org/10.1007/978-90-481-3817-3_5openalex-snapshot
Phosphine-Containing Planar Chiral Ferrocenes: Synthesis, Coordination Chemistry and Applications to Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1007/s10562-010-0383-3openalex-snapshot
Highly Efficient Rhodium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabenzonorbornadiene with Amine Nucleophiles
inferred← citeshttps://doi.org/10.1007/s10562-013-1136-xopenalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Oxabicyclic Alkenes with Carboxylic Acids
inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00095-7openalex-snapshot
Phosphorus Ligands
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00306-0openalex-snapshot
Furans and their Benzo Derivatives: Reactivity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.12.095openalex-snapshot
Discovery of μ-opioid selective ligands derived from 1-aminotetralin scaffolds made via metal-catalyzed ring-opening reactions
inferred← citeshttps://doi.org/10.1016/j.cclet.2006.12.003openalex-snapshot
Rhodium-catalyzed asymmetric ring opening of azabenzonorbornadiene with substituted piperazine nucleophiles
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2003
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.heliyon.2023.e20935openalex-snapshot
On K-Banhatti indices and entropy measure for rhodium (III) chloride via linear regression models
inferred← citeshttps://doi.org/10.1016/j.ica.2007.03.029openalex-snapshot
PGSE diffusion NMR studies on mononuclear and dinuclear cationic platinum salts of (S)-MeO-Biphep and (R)-p-tolyl-BINAP
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.11.023openalex-snapshot
Highly enantioselective catalytic asymmetric ring opening reaction employing the Daniphos ligand
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.06.032openalex-snapshot
A sub-stoichiometric tungsten-mediated Pauson–Khand reaction: Scope and limitations
inferred← citeshttps://doi.org/10.1016/j.pnmrs.2006.09.001openalex-snapshot
Ion pairing using PGSE diffusion methods
inferred← citeshttps://doi.org/10.1016/j.tet.2007.04.031openalex-snapshot
Tandem intramolecular benzyne–furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester
inferred← citeshttps://doi.org/10.1016/j.tet.2009.03.090openalex-snapshot
A relative approach for determining ring strain energies of heterobicyclic alkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2011.01.009openalex-snapshot
Transesterification catalyzed by iron(III) β-diketonate species
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.029openalex-snapshot
A simple route to derivatives of benzo[j]fluoranthene
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.12.024openalex-snapshot
Enantioselective synthesis of chiral 1,2-diamines by the catalytic ring opening of azabenzonorbornadienes: application in the preparation of new chiral ligands
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.03.017openalex-snapshot
Tunable chiral monophosphines as ligands in enantioselective rhodium-catalyzed ring-opening of oxabenzonorbornadienes with amines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.06.007openalex-snapshot
Kinetic resolution of C1-substituted oxabenzonorbornadienes by Ir-catalyzed asymmetric [2+2] cycloaddition reactions with arylacetylenes
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.tetasy.2016.11.004openalex-snapshot
Rhodium/zinc co-catalyzed asymmetric ring opening reactions of oxabenzonorbornadienes with carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.018openalex-snapshot
Synthesis of an octahydroindolinone scaffold for a diversity-based chemical compound library
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.2015.10.076openalex-snapshot
Diels–Alder reactions of arynes in situ generated from DA reaction between bis-1,3-diynes and alkynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.150990openalex-snapshot
Iridium-catalyzed ring-opening reactions of unsymmetrical oxabenzonorbornadienes with water and alcohol nucleophiles
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/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(05)80049-2openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.accounts.5c00289openalex-snapshot
Emerging Capabilities of Nonclassical Noncovalent Interactions and Asymmetric Catalysis in Stereoselective Glycosylations and Carbohydrate Functionalizations
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03034openalex-snapshot
Copper-Catalyzed Cycloaddition of Heterobicyclic Alkenes with Diaryl Disulfides to Synthesize Dihydrobenzo[b]thiophene Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02576openalex-snapshot
Copper-Catalyzed Hydroamination of Oxa- and Azabenzonorbornadienes with Pyrazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02836openalex-snapshot
Chiral Bicyclic NHC/Rh Complexes and Their Application to Catalytic Asymmetric Ring-Opening Reaction of Oxabenzonorbornadienes with Amines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01347openalex-snapshot
Synthesis and Application of Planar Chiral NHC/Rh Complexes Bearing CoC4Ph4 Group
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.5b00065openalex-snapshot
Platinum-Catalyzed Asymmetric Ring-Opening Reactions of Oxabenzonorbornadienes with Phenols
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02582openalex-snapshot
Asymmetric Ring Opening of Oxabicyclic Alkenes: Enhanced Rhodium Catalysis Using Camphor-Derived NHC Ligands Featuring Pyridine Coordination
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02678openalex-snapshot
Rh-Catalyzed Asymmetric Hydrogenation of 1,2-Dicyanoalkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03038openalex-snapshot
Asymmetric Ring-Opening Reactions of Aza- and Oxa-bicyclic Alkenes with Boronic Acids Using a Palladium/Zinc Co-catalytic System
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00178openalex-snapshot
Iridium-Catalyzed Anti-Stereoselective Asymmetric Ring-Opening Reactions of Azabenzonorbornadienes with Carboxylic Acids
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.1c00017openalex-snapshot
The Mechanism and Origin of Enantioselectivity in the Rhodium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabicyclic Alkenes with Organoboronic Acids: A DFT Investigation
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.organomet.5b00551openalex-snapshot
Palladium/Silver-Cocatalyzed Tandem Reactions of Oxabenzonorbornadienes with Substituted Arylacetylenes: A Simple Method for the Preparation of 1,2-Diarylethanones and 1,2-Diarylacetylenes
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00239openalex-snapshot
Enantioselective Iridium-Catalyzed Ring Opening of Low-Activity Azabenzonorbornadienes with Amines
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00770openalex-snapshot
Chiral NHC-Iridium Complexes and Their Performance in Enantioselective Intramolecular Hydroamination and Ring-Opening Amination Reactions
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.5c00971openalex-snapshot
Asymmetric Multi-Atom Insertion of Esters via Rh-Catalyzed Ring Opening of Oxabicyclic Alkenes
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.6b02592openalex-snapshot
Iridium-Catalyzed Asymmetric Addition of Thiophenols to Oxabenzonorbornadienes
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.9b02819openalex-snapshot
Rhodium-Catalyzed Enantioselective Synthesis of Oxazinones via an Asymmetric Ring Opening-Lactonization Cascade of Oxabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.0c03493openalex-snapshot
Advances in Nucleophilic Allylic Fluorination
inferred← citeshttps://doi.org/10.1021/acscatal.0c05554openalex-snapshot
Synergistic Dinuclear Rhodium Induced Rhodium-Walking Enabling Alkene Terminal Arylation: A Theoretical Study
inferred← citeshttps://doi.org/10.1021/acscatal.2c02410openalex-snapshot
Carboxylic Acids as Building Blocks in Catalytic Asymmetric Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.2c05029openalex-snapshot
Chromium-Catalyzed syn-Selective Ring-Opening Aryl-/Alkylation of 7-Oxabenzonorbornadiene Derivatives with Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acscatal.5c08795openalex-snapshot
Regio- and Enantioselective Rhodium-Catalyzed Sulfonylation of gem -Difluorinated Cyclopropanes
inferred← citeshttps://doi.org/10.1021/acscatal.6b02208openalex-snapshot
Copper-Catalyzed Asymmetric Borylative Ring Opening of Diazabicycles
inferred← citeshttps://doi.org/10.1021/acscatal.7b02508openalex-snapshot
Developing NHC-Iridium Catalysts for the Highly Efficient Enantioselective Intramolecular Hydroamination Reaction
inferred← citeshttps://doi.org/10.1021/ar600021zopenalex-snapshot
New Catalytic Reactions of Oxa- and Azabicyclic Alkenes
inferred← citeshttps://doi.org/10.1021/ja0577701openalex-snapshot
Rhodium-Catalyzed Ring-Opening Reactions of N-Boc-Azabenzonorbornadienes with Amine Nucleophiles
inferred← citeshttps://doi.org/10.1021/ja068488copenalex-snapshot
Rhodium-Catalyzed Asymmetric Cyclodimerization of Oxa- and Azabicyclic Alkenes
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/jo200147hopenalex-snapshot
Developing a Diastereoselective Intramolecular [4 + 3] Cycloaddition of Nitrogen-Stabilized Oxyallyl Cations Derived from N-Sulfonyl-Substituted Allenamides
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/jo402386kopenalex-snapshot
Platinum(II)-Catalyzed Asymmetric Ring-Opening Addition of Arylboronic Acids to Oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.1021/jo500821mopenalex-snapshot
Nickel-Catalyzed Asymmetric Ring Opening of Oxabenzonorbornadienes with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/jo701290bopenalex-snapshot
Features and Applications of [Rh(CO)2Cl]2-Catalyzed Alkylations of Unsymmetrical Allylic Substrates
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/ol0712531openalex-snapshot
Ruthenium(II)-Catalyzed Cyclization of Azabenzonorbornadienes with Alkynes
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/ol402804topenalex-snapshot
Rh-Catalyzed Highly Enantioselective Hydroalkynylation Reaction of Norbornadiene Derivatives
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/ol7030334openalex-snapshot
Gold-Catalyzed [4+3]-Annulation of Oxabicyclic Benzenes with 2-Substituted Allylsilanes through Tandem Allylation and Cyclization
inferred← citeshttps://doi.org/10.1021/ol801549topenalex-snapshot
Rhodium-Catalyzed Asymmetric Ring-Opening Alkynylation of Azabenzonorbornadienes
inferred← citeshttps://doi.org/10.1021/ol801768eopenalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening Reactions ofN-Boc-azabenzonorbornadiene with Secondary Amine Nucleophiles
inferred← citeshttps://doi.org/10.1021/om100384qopenalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabenzonorbornadienes with Amine Nucleophiles
inferred← citeshttps://doi.org/10.1021/om100722fopenalex-snapshot
Iridium-Catalyzed Anti-Stereocontrolled Asymmetric Ring Opening of Azabicyclic Alkenes with Primary Aromatic Amines
inferred← citeshttps://doi.org/10.1021/om3000295openalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Azabicyclic Alkenes with Phenols
inferred← citeshttps://doi.org/10.1021/om7004518openalex-snapshot
Construction of Isochromenes via a Ruthenium-Catalyzed Reaction of Oxabenzonorbornenes with Propargylic Alcohols
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/10.1039/b813501kopenalex-snapshot
Impact of the linker groups in bis(7-azaindol-1-yl) chelate ligands on structures and stability of Pt(N,N-L)R2 complexes
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/c3cc46009fopenalex-snapshot
Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst
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/c4ob00704bopenalex-snapshot
Rhodium( iii )-catalyzed coupling of N-sulfonyl 2-aminobenzaldehydes with oxygenated allylic olefins through C–H activation
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/c5ob02422fopenalex-snapshot
Highly efficient asymmetric hydrogenation of cyano-substituted acrylate esters for synthesis of chiral γ-lactams and amino acids
inferred← citeshttps://doi.org/10.1039/c7gc03772dopenalex-snapshot
Water-promoted synthesis of fused bicyclic triazolines and naphthols from oxa(aza)bicyclic alkenes and transformation via a novel ring-opening/rearrangement reaction
inferred← citeshttps://doi.org/10.1039/c7ob00175dopenalex-snapshot
Palladium/zinc co-catalyzed asymmetric transfer hydrogenation of oxabenzonorbornadienes with alcohols as hydrogen sources
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/c8qo01403eopenalex-snapshot
Ir-Catalyzed ring-opening of oxa(aza)benzonorbornadienes with water or alcohols
inferred← citeshttps://doi.org/10.1039/c9qo00660eopenalex-snapshot
1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes
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/d0ob00659aopenalex-snapshot
Copper-catalyzed diastereoselective hydrothioetherification of oxa(aza)benzonorbornadienes
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/10.1055/s-0042-1751405openalex-snapshot
Benzo-Fused 7-Oxabicyclo[2.2.1]heptane-2,3-diol Derivatives as Universal Linkers for Solid-Phase Oligonucleotide Synthesis
inferred← citeshttps://doi.org/10.1139/cjc-2014-0140openalex-snapshot
1,3-Dipolar cycloadditions of nitrile oxides with 7-oxa- and 7-azabenzonorbornadienes
inferred← citeshttps://doi.org/10.1139/cjc-2014-0274openalex-snapshot
1,3-Dipolar cycloaddition of nitrile oxides with C1-substituted 7-oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.12677/jocr.2017.51008openalex-snapshot
Progress on Asymmetric C-O Bond Formation with Phenols
inferred← citeshttps://doi.org/10.2174/1570179417666210105121115openalex-snapshot
Chemistry of Unsymmetrical C1-Substituted Oxabenzonorbornadienes
inferred← citeshttps://doi.org/10.3390/molecules201219748openalex-snapshot
Iridium-Catalyzed Asymmetric Ring-Opening of Oxabenzonorbornadienes with N-Substituted Piperazine Nucleophiles
inferred← citeshttps://doi.org/10.3762/bjoc.5.53openalex-snapshot
Iridium-catalyzed asymmetric ring-opening reactions of oxabicyclic alkenes with secondary amine nucleophiles
inferred← citeshttps://doi.org/10.3987/com-06-s(w)36openalex-snapshot
Cycloaddition Reactions of Amino-Acid Derived Cross-Conjugated Trienes: Stereoselective Synthesis of Novel Heterocyclic Scaffolds
inferred← citeshttps://doi.org/10.70675/9429a4c2z8e1bz49b8z8f2fz02f198da2c66openalex-snapshot
Développement de nouvelles méthodes d'amination intermoléculaire d'énamides par transfert de nitrènes catalysé par le rhodium
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.