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Quinap and Congeners: Atropos PN ligands for Asymmetric Catalysis

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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1521-3765(19990401)5:4<1320::aid-chem1320>3.0.co;2-#openalex-snapshot

The Scope of Catalytic Asymmetric Hydroboration/Oxidation with Rhodium Complexes of 1,1′-(2-Diarylphosphino-1-naphthyl)isoquinolines

inferredcites →https://doi.org/10.1002/(sici)1521-3765(20000515)6:10<1840::aid-chem1840>3.0.co;2-6openalex-snapshot

Catalytic Asymmetric Hydroboration/Amination and Alkylamination with Rhodium Complexes of 1,1′-(2-Diarylphosphino-1-naphthyl)isoquinoline

inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2535::aid-anie2535>3.0.co;2-mopenalex-snapshot

Enantioselective Synthesis of Propargylamines by Copper-Catalyzed Addition of Alkynes to Enamines

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Chirale Phosphinoaryldihydrooxazole als Liganden in der asymmetrischen Katalyse: Pd‐katalysierte allylische Substitution

inferredcites →https://doi.org/10.1002/anie.199513361openalex-snapshot

Transition Metal Catalyzed Diboration of Vinylarenes

inferredcites →https://doi.org/10.1002/anie.199721081openalex-snapshot

Palladium‐Catalyzed Allylic Alkylation with Phosphinoaryldihydrooxazole Ligands: First Evidence and NMR Spectroscopic Structure Determination of a Primary Olefin–Pd0 Complex

inferredcites →https://doi.org/10.1002/anie.200352578openalex-snapshot

Enantioselective, Copper( I )‐Catalyzed Three‐Component Reaction for the Preparation of Propargylamines

inferredcites →https://doi.org/10.1002/anie.200461286openalex-snapshot

Readily Available Biaryl P,N Ligands for Asymmetric Catalysis

inferredcites →https://doi.org/10.1002/anie.201001918openalex-snapshot

Nickel‐Catalyzed Regio‐ and Enantioselective Annulation Reactions of 1,2,3,4‐Benzothiatriazine‐1,1(2 H )‐dioxides with Allenes

inferredcites →https://doi.org/10.1002/anie.201101941openalex-snapshot

Transition‐Metal‐Free Diboration Reaction by Activation of Diboron Compounds with Simple Lewis Bases

inferredcites →https://doi.org/10.1002/anie.201102398openalex-snapshot

NHC‐Cu‐Catalyzed Enantioselective Hydroboration of Acyclic and Exocyclic 1,1‐Disubstituted Aryl Alkenes

inferredcites →https://doi.org/10.1002/anie.201308699openalex-snapshot

Enantioselective Double Manipulation of Tetrahydroisoquinolines with Terminal Alkynes and Aldehydes under Copper(I) Catalysis

inferredcites →https://doi.org/10.1002/cbic.201200711openalex-snapshot

Biology‐Oriented Synthesis of a Tetrahydroisoquinoline‐Based Compound Collection Targeting Microtubule Polymerization

inferredcites →https://doi.org/10.1002/chem.200204691openalex-snapshot

Synthesis of Enantiomerically Enriched Propargylamines by Copper‐Catalyzed Addition of Alkynes to Enamines

inferredcites →https://doi.org/10.1002/chem.200390012openalex-snapshot

How To Turn the Catalytic Asymmetric Hydroboration Reaction of Vinylarenes into a Recyclable Process

inferredcites →https://doi.org/10.1002/chem.200400574openalex-snapshot

In Quest of Factors That Control the Enantioselective Catalytic Markovnikov Hydroboration/Oxidation of Vinylarenes

inferredcites →https://doi.org/10.1002/chem.200501233openalex-snapshot

Practical Highly Enantioselective Synthesis of Propargylamines through a Copper‐Catalyzed One‐Pot Three‐Component Condensation Reaction

inferredcites →https://doi.org/10.1002/ejoc.200800650openalex-snapshot

Synthesis, Resolution, and Application of Cyclobutyl‐ and Adamantyl‐Quinazolinap Ligands

inferredcites →https://doi.org/10.1002/ejoc.201000794openalex-snapshot

Synthesis and Post‐Resolution Modification of New Axially Chiral Ligands for Asymmetric Catalysis

inferredcites →https://doi.org/10.1016/0957-4166(95)00344-oopenalex-snapshot

Nonlinear effects involving two competing pseudo-enantiomeric catalysts: Example in asymmetric dihydroxylation of olefins

inferredcites →https://doi.org/10.1016/j.tet.2005.02.008openalex-snapshot

Enantioselective synthesis of axially chiral 1-(1-naphthyl)isoquinolines and 2-(1-naphthyl)pyridines through sulfoxide ligand coupling reactions

inferredcites →https://doi.org/10.1016/j.tet.2005.08.064openalex-snapshot

Preparation of functionalized primary chiral amines and amides via an enantioselective three-component synthesis of propargylamines

inferredcites →https://doi.org/10.1016/j.tetasy.2005.02.016openalex-snapshot

Metal promoted asymmetry in the 1,2-diboroethylarene synthesis: diboration versus dihydroboration

inferredcites →https://doi.org/10.1016/j.tetasy.2010.06.012openalex-snapshot

Rhodium-catalysed hydroboration employing new Quinazolinap ligands; an investigation into electronic effects

inferredcites →https://doi.org/10.1016/s0040-4020(01)89381-9openalex-snapshot

Mechanistic and synthetic studies in catalytic allylic alkylation with palladium complexes of 1-(2-diphenylphosphino-1-naphthyl)isoquinoline

inferredcites →https://doi.org/10.1016/s0040-4020(97)00016-1openalex-snapshot

Synthesis of 1-methyl-2-diphenylphosphino-3-(1′-isoquinolyl)indole; an easily racemised ligand giving insights into catalytic asymmetric allylation

inferredcites →https://doi.org/10.1016/s0040-4039(00)60774-8openalex-snapshot

Phosphinoaryl- and phosphinoalkyloxazolines as new chiral ligands for enantioselective catalysis: Very high enantioselectivity in palladium catalyzed allylic substitutions

inferredcites →https://doi.org/10.1016/s0040-4039(00)76748-7openalex-snapshot

Catalysis of allylic substitutions by Pd complexes of oxazolines containing an additional P, S, or Se Center. X-ray crystal structures and solution structures of chiral π-allyl palladium complexes of phosphinoaryloxazolines

inferredcites →https://doi.org/10.1016/s0040-4039(00)93403-8openalex-snapshot

Asymmetric palladium catalysed allylic substitution using phosphorus containing oxazoline ligands

inferredcites →https://doi.org/10.1016/s0040-4039(00)93563-9openalex-snapshot

Chiral Co(II) and Mn(II) catalysts for the 1,3-dipolar cycloaddition reactions of azomethine ylides derived from arylidene imines of glycine

inferredcites →https://doi.org/10.1016/s0957-4166(00)80183-4openalex-snapshot

Synthesis and resolution of 1-(2-diphenylphosphino-1-naphthyl)isoquinoline; a PN chelating ligand for asymmetric catalysis.

inferredcites →https://doi.org/10.1016/s0957-4166(00)82305-8openalex-snapshot

Synthesis and easy racemisation of an atropisomerically chiral phosphinamine

inferredcites →https://doi.org/10.1016/s0957-4166(00)86112-1openalex-snapshot

Asymmetric hydroboration of styrenes catalyzed by cationic chiral phosphine-rhodium(I) complexes

inferredcites →https://doi.org/10.1016/s0957-4166(97)00556-9openalex-snapshot

Synthesis of 1′-(2-(diarylphosphino)1-naphthyl)isoquinolines; variation of the aryl substituent

inferredcites →https://doi.org/10.1021/ar00084a003openalex-snapshot

Asymmetric synthesis catalyzed by transition-metal complexes with functionalized chiral ferrocenylphosphine ligands

inferredcites →https://doi.org/10.1021/ar00178a005openalex-snapshot

BINAP: an efficient chiral element for asymmetric catalysis

inferredcites →https://doi.org/10.1021/cs300146xopenalex-snapshot

Nonlinear Effects with Diastereomeric Ligand Mixtures in Enantioselective, Catalytic Additions of Terminal Alkynes Involving Copper–PINAP Complexes

inferredcites →https://doi.org/10.1021/ja00076a081openalex-snapshot

Platinum(0)-catalyzed diboration of alkynes

inferredcites →https://doi.org/10.1021/ja035851wopenalex-snapshot

Rhodium-Catalyzed Enantioselective Diboration of Simple Alkenes

inferredcites →https://doi.org/10.1021/ja036558zopenalex-snapshot

Catalytic Asymmetric [3+2] Cycloaddition of Azomethine Ylides. Development of a Versatile Stepwise, Three-Component Reaction for Diversity-Oriented Synthesis

inferredcites →https://doi.org/10.1021/ja049761iopenalex-snapshot

Regio- and Enantiocontrol in the Room-Temperature Hydroboration of Vinyl Arenes with Pinacol Borane

inferredcites →https://doi.org/10.1021/ja052411ropenalex-snapshot

Catalytic, Enantioselective, Conjugate Alkyne Addition

inferredcites →https://doi.org/10.1021/ja407689aopenalex-snapshot

Design, Preparation, and Implementation of an Imidazole-Based Chiral Biaryl P,N-Ligand for Asymmetric Catalysis

inferredcites →https://doi.org/10.1021/ja4087819openalex-snapshot

Dynamic Kinetic Cross-Coupling Strategy for the Asymmetric Synthesis of Axially Chiral Heterobiaryls

inferredcites →https://doi.org/10.1021/ja409383fopenalex-snapshot

Asymmetric Synthesis of QUINAP via Dynamic Kinetic Resolution

inferredcites →https://doi.org/10.1021/ja900722qopenalex-snapshot

Controlling Axial Conformation in 2-Arylpyridines and 1-Arylisoquinolines: Application to the Asymmetric Synthesis of QUINAP by Dynamic Thermodynamic Resolution

inferredcites →https://doi.org/10.1021/jo0159542openalex-snapshot

A New Atropisomeric P,N Ligand for Rhodium-Catalyzed Asymmetric Hydroboration

inferredcites →https://doi.org/10.1021/jo035392hopenalex-snapshot

On the Origin of Regio- and Stereoselectivity in the Rhodium-Catalyzed Vinylarenes Hydroboration Reaction

inferredcites →https://doi.org/10.1021/jo049195+openalex-snapshot

Preparation and Resolution of a Modular Class of Axially Chiral Quinazoline-Containing Ligands and Their Application in Asymmetric Rhodium-Catalyzed Olefin Hydroboration

inferredcites →https://doi.org/10.1021/jo051651mopenalex-snapshot

Rh-Catalyzed Enantioselective Diboration of Simple Alkenes: Reaction Development and Substrate Scope

inferredcites →https://doi.org/10.1021/ol036219aopenalex-snapshot

Catalytic Asymmetric Carbohydroxylation of Alkenes by a Tandem Diboration/Suzuki Cross-Coupling/Oxidation Reaction

inferredcites →https://doi.org/10.1021/ol0526165openalex-snapshot

Enantioselective Addition of Terminal Alkynes to Isolated Isoquinoline Iminiums

inferredcites →https://doi.org/10.1021/ol060876wopenalex-snapshot

Highly Enantioselective Access to Primary Propargylamines: 4-Piperidinone as a Convenient Protecting Group

inferredcites →https://doi.org/10.1021/ol300296kopenalex-snapshot

Catalytic Asymmetric Synthesis of Optically Active Allenes from Terminal Alkynes

inferredcites →https://doi.org/10.1021/op034007nopenalex-snapshot

Practical Preparation and Resolution of 1-(2‘-Diphenylphosphino-1‘-naphthyl)isoquinoline: A Useful Ligand for Catalytic Asymmetric Synthesis

inferredcites →https://doi.org/10.1038/nature12781openalex-snapshot

Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling

inferredcites →https://doi.org/10.1039/b111175bopenalex-snapshot

Efficient kinetic resolution in hydroboration of 1,2-dihydronaphthalenes

inferredcites →https://doi.org/10.1039/b508292gopenalex-snapshot

Regiochemical control of the catalytic asymmetric hydroboration of 1,2-diarylalkenes

inferredcites →https://doi.org/10.1039/b810936bopenalex-snapshot

Electronically varied quinazolinaps for asymmetric catalysis

inferredcites →https://doi.org/10.1039/b900741eopenalex-snapshot

Axially chiral P-N ligands for the copper catalyzed β-borylation of α,β-unsaturated esters

inferredcites →https://doi.org/10.1039/b913336dopenalex-snapshot

Expedient synthesis of 3-hydroxyisoquinolines and 2-hydroxy-1,4-naphthoquinones via one-pot aryne acyl-alkylation/condensation

inferredcites →https://doi.org/10.1039/c2sc21617eopenalex-snapshot

Catalytic asymmetric synthesis of highly substituted pyrrolizidines

inferredcites →https://doi.org/10.1039/c39950000395openalex-snapshot

Contrasting behaviour of related palladium complex-derived resolving agents. 8-H conformational locking of the 1-naphthyl side-chain

inferredcites →https://doi.org/10.1039/c3cs60302dopenalex-snapshot

P,N ligands in asymmetric catalysis

inferredcites →https://doi.org/10.1039/c3ob40360bopenalex-snapshot

Meta-analysis in asymmetric catalysis. Influence of chelate geometry on the roles of PN chelating ligands

inferredcites →https://doi.org/10.1055/s-2001-18080openalex-snapshot

A Facile and Versatile Route to 2-Substituted-4(3H)-Quinazolinones and Quinazolines

inferredcites →https://doi.org/10.1107/s0108768102003890openalex-snapshot

The Cambridge Structural Database: a quarter of a million crystal structures and rising

inferredcites →https://doi.org/10.1246/bcsj.80.1635openalex-snapshot

Stereoselective Conjugate Addition Reactions Using In Situ Metallated Terminal Alkynes and the Development of Novel Chiral P,N-Ligands

inferredcites →https://doi.org/10.3891/acta.chem.scand.26-0929openalex-snapshot

Activation Parameters for Inversion of 1-(1-Naphthyl)-isoquinoline. I. Synthesis and Optical Resolution of 1-(1-Naphthyl)-isoquinoline.

What points at this work

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

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Synthesis and Evaluation of the Biological Properties of Novel Boron-Containing Capsaicin Derivatives on Human Cancer Cell Lines

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Quinazolinap

inferred← citeshttps://doi.org/10.1002/047084289x.rn02108openalex-snapshot

Isoquinoline, 1-[2-(Diphenylphosphino)-1-naphthalenyl-], (R and S )

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Atroposelective Synthesis of PINAP via Dynamic Kinetic Asymmetric Transformation

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Advances in the Catalytic Asymmetric Synthesis of Atropisomeric Hexatomic N‐Heterobiaryls

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Synthesis of Triaminocyclopentadienyl Iron(II) Tricarbonyl Complexes and Application to the Synthesis of Aminophosphines

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The Phosphinoboration Reaction

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Enantioselective Copper‐Catalyzed Quinoline Alkynylation

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Biocatalytic Dynamic Kinetic Resolution for the Synthesis of Atropisomeric Biaryl N‐Oxide Lewis Base Catalysts

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Heavily Substituted Atropisomeric Diarylamines by Unactivated Smiles Rearrangement of N‐Aryl Anthranilamides

inferred← citeshttps://doi.org/10.1002/ange.202102642openalex-snapshot

Configuration Sampling With Five‐Membered AtropisomericP,N‐Ligands

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Atroposelective P III /P V =O Redox Catalysis for the Isoquinoline‐Forming Staudinger–aza‐Wittig Reaction

inferred← citeshttps://doi.org/10.1002/ange.202502131openalex-snapshot

Rhodium‐Catalyzed Atroposelective Synthesis of Axially Chiral 1‐Aryl Isoquinolines via De Novo Isoquinoline Formation

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Atroposelective Pd(0)‐Catalyzed Direct Intermolecular C─H Arylation of Thiazole N ‐Oxides Provides Access to Heterobiaryls

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The Phosphinoboration Reaction

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Enantioselective Copper‐Catalyzed Quinoline Alkynylation

inferred← citeshttps://doi.org/10.1002/anie.201605486openalex-snapshot

Biocatalytic Dynamic Kinetic Resolution for the Synthesis of Atropisomeric Biaryl N‐Oxide Lewis Base Catalysts

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Heavily Substituted Atropisomeric Diarylamines by Unactivated Smiles Rearrangement of N ‐Aryl Anthranilamides

inferred← citeshttps://doi.org/10.1002/anie.202102642openalex-snapshot

Configuration Sampling With Five‐Membered AtropisomericP,N‐Ligands

inferred← citeshttps://doi.org/10.1002/anie.202309053openalex-snapshot

Atroposelective P III /P V =O Redox Catalysis for the Isoquinoline‐Forming Staudinger–aza‐Wittig Reaction

inferred← citeshttps://doi.org/10.1002/anie.202502131openalex-snapshot

Rhodium‐Catalyzed Atroposelective Synthesis of Axially Chiral 1‐Aryl Isoquinolines via De Novo Isoquinoline Formation

inferred← citeshttps://doi.org/10.1002/anie.6888467openalex-snapshot

Atroposelective Pd(0)‐Catalyzed Direct Intermolecular C─H Arylation of Thiazole N ‐Oxides Provides Access to Heterobiaryls

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Chiral P,N‐ligands for the highly enantioselective addition of diethylzinc to aromatic aldehydes

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Filling the Gaps in the Challenging Asymmetric Hydroboration of 1,1‐Disubstituted Alkenes with Simple Phosphite‐Based Phosphinooxazoline Iridium Catalysts

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Chiral Phosphoric Acid: A Powerful Organocatalyst for the Asymmetric Synthesis of Heterocycles with Chiral Atropisomerism

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Catalytic Kinetic Resolution of Biaryl Compounds

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ChemInform Abstract: Quinap and Congeners: Atropos PN Ligands for Asymmetric Catalysis

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Skeletal Editing of Cyclic Molecules Using Nitrenes

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The Preparation and Resolution of Novel Axially Chiral Pyrazine‐Containing P,N Ligands for Asymmetric Catalysis and Their Application in Palladium‐Catalysed Allylic Substitution

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Palladium‐Catalyzed O‐Arylation Reaction Using Different Heterogeneous Catalyst Systems: The Role of Support

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Adaptable P–X Biaryl Phosphite/Phosphoroamidite‐Containing Ligands for Asymmetric Hydrogenation and C–X Bond‐Forming Reactions: Ligand Libraries with Exceptionally Wide Substrate Scope

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Aminoalkyl-phosphine (P,N) ligands with pentane-2,4-diyl backbone in asymmetric allylic substitution reactions

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Expeditious synthesis and applications of isoquinoline ring-modified Quinap derivatives

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Modular synthesis of polyfunctionalized axial-chiral 2-arylpyridines via cobalt-catalyzed asymmetric [2 + 2 + 2] cycloaddition of diynes and nitriles

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Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications

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Dynamic kinetic resolution and dynamic kinetic asymmetric transformation of atropisomeric biaryls

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Efficient stereochemical communication in phosphine-amine palladium-complexes: Exploration of N-substituent effects in coordination chemistry and catalysis

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Polydentate P, N-based ligands for palladium-catalyzed cross-coupling reactions

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Synthesis and evaluation of the biological properties of boron-containing and boron-omitted capsaicin derivatives on human cancer cell lines

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Asymmetric Michael addition of diphenylphosphine to β,γ-unsaturated α-keto esters catalyzed by a P-stereogenic pincer-Pd complex

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Substituent effects on axial chirality in 1-aryl-3,4-dihydroisoquinolines: controlling the rate of bond rotation

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Synthetic and mechanistic studies in enantioselective allylic substitutions catalysed by palladium complexes of a modular class of axially chiral quinazoline-containing ligands

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The preparation of ferrocene-containing phosphinamine ligands possessing central and planar chirality and their application in palladium-catalysed allylic substitution

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Enantioselective Cu(II)-catalyzed Henry reactions with chiral cyclohexane-based amidophosphine ligands

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Diboron(4) Compounds: From Structural Curiosity to Synthetic Workhorse

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Catalytic Approach toward Chiral P,N-Chelate Complexes Utilizing the Asymmetric Hydrophosphination Protocol

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Synthetic, Computational, and Experimental Studies of a Class 3 Atropisomeric α-Naphthyl Tropone

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Palladium-Catalyzed Multicomponent Carbonylative Cyclization toward Ynone-Functionalized Isoquinolinones

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Enantioselective Catalytic Asymmetric A3 Coupling with Phosphino-Imidazoline Ligands

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Asymmetric Synthesis of Quinoline-Naphthalene Atropisomers by Central-to-Axial Chirality Conversion

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Enantioselective Construction of Quinoxaline-Based Heterobiaryls and P,N-Ligands via Chirality Transfer Strategy

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Enantioselective Construction of C–C Axially Chiral Quinazolinones via Chirality Exchange and Phase-Transfer Catalysis

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Enantioselective Construction of Axially Chiral Azepine-Containing P,N-Ligands from l -Alanine

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Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands

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Expedient Access to Polyaromatic Biaryls by Unconventional Ag-Catalyzed Cycloaromatization of Alkynylthiophenes and Au-Catalyzed Double C–H Activation

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Palladium-Catalyzed Modular Assembly of P-Stereogenic and Axially Chiral Phosphinooxazoles (PHOX) Ligands by C–P Bond Cleavage/Intermolecular C(sp2)–H Bond Functionalization

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Relay PHOS: Ligands with Fluxional Chirality in Asymmetric Palladium-Catalyzed Allylic Alkylation

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Halogen-Bond-Assisted NHC-Catalyzed (Dynamic) Kinetic Resolution for the Atroposelective Synthesis of Heterobiaryls

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Construction of Axially Chiral 4-Aminoquinolines by Cycloaddition and Central-to-Axial Chirality Conversion

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Nickel-Catalyzed Atroposelective Synthesis of Axially Chiral Heterobiaryls via De Novo Benzene Formation

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Rh(II)-Catalyzed Site-Selective Insertion of Quinoid Carbene into Quinoline N -Oxides to Synthesize METHOX-Inspired Heterobiaryls

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00707openalex-snapshot

Troponoid Atropisomerism: Studies on the Configurational Stability of Tropone-Amide Chiral Axes

inferred← citeshttps://doi.org/10.1021/acscatal.3c00751openalex-snapshot

Rh(III)-Catalyzed Atroposelective C–H Iodination of 1-Aryl Isoquinolines

inferred← citeshttps://doi.org/10.1021/acscatal.4c00519openalex-snapshot

Iridium-Catalyzed Regiodivergent Atroposelective C–H Alkylation of Heterobiaryls with Alkenes

inferred← citeshttps://doi.org/10.1021/acscatal.4c07172openalex-snapshot

Dynamic Kinetic Reductive Grignard-Type Addition for the Construction of Axial and Central Chirality

inferred← citeshttps://doi.org/10.1021/acscatal.5c01663openalex-snapshot

Modular Assembly of Axially Chiral QUINAP Derivatives via Nickel-Catalyzed Enantioselective C–P Cross-Coupling

inferred← citeshttps://doi.org/10.1021/acscatal.6b00784openalex-snapshot

A Dynamic Kinetic C–P Cross–Coupling for the Asymmetric Synthesis of Axially Chiral P,N Ligands

inferred← citeshttps://doi.org/10.1021/acscatal.6b03427openalex-snapshot

Diastereofacial π-Stacking as an Approach To Access an Axially Chiral P,N-Ligand for Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1021/acscatal.7b00133openalex-snapshot

Incorporation of Axial Chirality into Phosphino-Imidazoline Ligands for Enantioselective Catalysis

inferred← citeshttps://doi.org/10.1021/acscatal.7b03759openalex-snapshot

Axially Chiral P,N-Ligands: Some Recent Twists and Turns

inferred← citeshttps://doi.org/10.1021/acscatal.8b04787openalex-snapshot

Asymmetric Hydrophosphination of Heterobicyclic Alkenes: Facile Access to Phosphine Ligands for Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1021/bk-2016-1236.ch006openalex-snapshot

Current Developments in the Catalyzed Hydroboration Reaction

inferred← citeshttps://doi.org/10.1021/jacs.0c08205openalex-snapshot

Rhodium-Catalyzed Atroposelective Oxidative C–H/C–H Cross-Coupling Reaction of 1-Aryl Isoquinoline Derivatives with Electron-Rich Heteroarenes

inferred← citeshttps://doi.org/10.1021/jacs.2c02563openalex-snapshot

Asymmetric Azide–Alkyne Cycloaddition with Ir(I)/Squaramide Cooperative Catalysis: Atroposelective Synthesis of Axially Chiral Aryltriazoles

inferred← citeshttps://doi.org/10.1021/jacs.3c05845openalex-snapshot

Nickel-Catalyzed Enantioconvergent Transformation of Anisole Derivatives via Cleavage of C–OMe Bond

inferred← citeshttps://doi.org/10.1021/jacs.4c15491openalex-snapshot

Atroposelective Diverse Remote meta -C–H Functionalization via Kinetic Resolution

inferred← citeshttps://doi.org/10.1021/jacs.5c07049openalex-snapshot

Diastereo- and Enantioselective Pd-Catalyzed C–P Coupling for Axially and P-Chiral Phosphine Oxides via Simultaneous Dynamic Kinetic Asymmetric Transformation and Kinetic Resolution

inferred← citeshttps://doi.org/10.1021/jacs.6b07972openalex-snapshot

Synthesis of IAN-type N,N-Ligands via Dynamic Kinetic Asymmetric Buchwald–Hartwig Amination

inferred← citeshttps://doi.org/10.1021/jacs.7b00363openalex-snapshot

Enantioselective Alkyne Conjugate Addition Enabled by Readily Tuned Atropisomeric P , N -Ligands

inferred← citeshttps://doi.org/10.1021/jacs.9b03862openalex-snapshot

Rhodium-Catalyzed Atroposelective C–H Arylation: Efficient Synthesis of Axially Chiral Heterobiaryls

inferred← citeshttps://doi.org/10.1039/c6cc08997fopenalex-snapshot

Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation

inferred← citeshttps://doi.org/10.1039/c6ra14367aopenalex-snapshot

A triazine-phosphite polymeric ligand bearing cage-like P,N-ligation sites: an efficient ligand in the nickel-catalyzed amination of aryl chlorides and phenols

inferred← citeshttps://doi.org/10.1039/c7dt02305gopenalex-snapshot

The phosphinoboration of carbodiimides, isocyanates, isothiocyanates and CO 2

inferred← citeshttps://doi.org/10.1039/c7ob02393fopenalex-snapshot

The synthesis of planar chiral pseudo-gem aminophosphine pre-ligands based on [2.2]paracyclophane

inferred← citeshttps://doi.org/10.1039/c9cs00253gopenalex-snapshot

Development of and recent advances in asymmetric A3 coupling

inferred← citeshttps://doi.org/10.1039/d0ob00421aopenalex-snapshot

Non-biaryl atropisomerism at the C–B bond in sterically hindered aminoarylboranes

inferred← citeshttps://doi.org/10.1039/d1ob02003jopenalex-snapshot

Phosphorylation of arenes, heteroarenes, alkenes, carbonyls and imines by dehydrogenative cross-coupling of P(O)–H and P(R)–H

inferred← citeshttps://doi.org/10.1039/d5qo00011dopenalex-snapshot

Biocatalytic atroposelective synthesis of heterobiaryls and heterobiaryl N -oxides via dynamic kinetic resolution

inferred← citeshttps://doi.org/10.1055/a-2021-9514openalex-snapshot

Enantioselective Synthesis of Axially Chiral 1-Arylisoquinolines by Iridium(I)-Catalyzed Hydroarylation of Alkynes

inferred← citeshttps://doi.org/10.1055/a-2837-6062openalex-snapshot

Nickel-Catalyzed Regio- and Enantioselective [4+2] Annulation toward Synthesis of Axially Chiral Isoquinolinyl and Pyridinyl Isoquinolinones

inferred← citeshttps://doi.org/10.1055/a-2913-5787openalex-snapshot

Design and Synthesis of Bulky PN Chiral Ligands Incorporating a Chiral Aniline Unit

inferred← citeshttps://doi.org/10.1126/sciadv.adw5850openalex-snapshot

Highly enantioselective synthesis controlled by spin-exchange interaction

inferred← citeshttps://doi.org/10.1134/s1070328426600439openalex-snapshot

Specific Features of Reactions of Anisoletricarbonylchromium(0) and Dimethoxyresorcinoltricarbonylchromium(0) with Acridine, Quinazoline, and Quinoxaline

inferred← citeshttps://doi.org/10.1139/cjc-2018-0193openalex-snapshot

Preliminary investigations into the synthesis and antimicrobial activities of boron-containing capsaicinoids

inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-5mccgopenalex-snapshot

Synthesis of Axially Chiral Biaryls via Pd(II)-Catalysed Direct C(sp2)-H Olefination and Arylation

inferred← citeshttps://doi.org/10.6023/cjoc202500018openalex-snapshot

Synthesis of Phosphine Oxides Bearing Multiple Chiral Elements via Catalyzed Asymmetric C—P Coupling

inferred← citeshttps://doi.org/10.70675/0272dbb6z53eez4f8cza452zd9c1e0021056openalex-snapshot

Hydrocarbures polycycliques aromatiques et chiralité : synthèse et modélisation

inferred← citeshttps://doi.org/10.70675/1169eb31zaa4ez4ea0z839czdd9595ba3d18openalex-snapshot

Synthèse hélicosélective de dioxa[6]hélicènes et design d’organocatalyseurs acides de brønsted P-stéréogènes originaux.

inferred← citeshttps://doi.org/10.70675/7c26fcc6z1fd8z43baz97e7z3c8883c78b4fopenalex-snapshot

Synthèse d’arylphosphines ortho-fonctionnalisées et leurs applications

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