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Effects of Halide Ligands and Protic Additives on Enantioselectivity and Reactivity in Rhodium-Catalyzed Asymmetric Ring-Opening Reactions

https://doi.org/10.1021/ja010262g
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What this work says

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

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Novel Diphosphinoiridium Catalysts for the Enantioselective Hydrogenation of N‐Arylketimines
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C2‐Symmetric Cationic Copper( II ) Complexes as Chiral Lewis Acids: Counterion Effects in the Enantioselective Diels–Alder Reaction
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Asymmetric Heck Reactions via Neutral Intermediates: Enhanced Enantioselectivity with Halide Additives Gives Mechanistic Insights
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Asymmetric allylic alkylation with palladium coordinated to a new optically active pyrazolylmethane ligand
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
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A remarkable anion effect on the enantioselectivity of the Pd-catalyzed allylic amination using ferrocenyl ligands
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Comprehensive Organometallic Chemistry
inferredcites →https://doi.org/10.1021/ic50024a007openalex-snapshot
Preparation and Properties of a Series of Halocarbonylrhodates
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/ja972594kopenalex-snapshot
The [IrCl(Diphosphine)]2/Fluoride System. Developing Catalytic Asymmetric Olefin Hydroamination
inferredcites →https://doi.org/10.1021/ja9828713openalex-snapshot
Regio- and Enantioselective Allylic Alkylation of an Unsymmetrical Substrate: A Working Model
inferredcites →https://doi.org/10.1021/ol005729ropenalex-snapshot
Rhodium-Catalyzed Asymmetric Ring Opening of Oxabicyclic Alkenes with Phenols
inferredcites →https://doi.org/10.1021/ol0060782openalex-snapshot
Rhodium-Catalyzed Ring Opening of Vinyl Epoxides with Alcohols and Aromatic Amines
inferredcites →https://doi.org/10.1039/c29710000418openalex-snapshot
A simple synthetic route to d 8 complexes of rhodium and iridium. An electronegativity scale for anionic ligands
inferredcites →https://doi.org/10.1039/c39880001466openalex-snapshot
Rhodium(I)-catalysed asymmetric hydrogenation of imines
inferredcites →https://doi.org/10.1055/s-1999-3106openalex-snapshot
Iridium Ferrocenyl Diphosphine Catalyzed Enantioselective Reductive Alkylation of a Hindered Aniline

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/anie.201600654openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201909596openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b915448popenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2cc31880fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3cc46009fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3ob40891dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3ob42199fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5ob02331aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0cc03158eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3cc00604bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/a-2152-0355openalex-snapshot
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(1R,2R,5R,6S)-5,6-Bis(4-methoxybenzyloxymethyl)-2-(methylphenylamino)cyclohex-3-enyl 4-bromobenzoate
inferred← citeshttps://doi.org/10.1107/s1600536802008115openalex-snapshot
Benzenesulfonyl(1-hydroxy-1,2-dihydronaphthalen-2-yl)acetonitrile
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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
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