On the public citation graph
Enantioselective Friedel−Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)−Zn(II) Complex
0 signed · 185 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/0471224480openalex-snapshot
The Nitro Group in Organic Synthesis
inferredcites →https://doi.org/10.1002/1099-0690(200206)2002:12<1877::aid-ejoc1877>3.0.co;2-uopenalex-snapshot
Asymmetric Michael Additions to Nitroalkenes
inferredcites →https://doi.org/10.1002/1521-3773(20010105)40:1<160::aid-anie160>3.0.co;2-sopenalex-snapshot
Catalytic Asymmetric Friedel-Crafts Alkylation of beta,gamma-Unsaturated alpha-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes This work was made possible by a grant from the Danish National Research Foundation.
inferredcites →https://doi.org/10.1002/anie.200301679openalex-snapshot
New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
inferredcites →https://doi.org/10.1002/anie.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
inferredcites →https://doi.org/10.1002/chir.20089openalex-snapshot
Application of lipases in kinetic resolution of racemates
inferredcites →https://doi.org/10.1002/chir.20189openalex-snapshot
Catalytic enantioselective addition of indoles to arylnitroalkenes: An effective route to enantiomerically enriched tryptamine precursors
inferredcites →https://doi.org/10.1002/med.2610150103openalex-snapshot
Phenserine and ring C hetero‐analogues: Drug candidates for the treatment of Alzheimer's disease
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00065-2openalex-snapshot
Friedel–Crafts Alkylations
inferredcites →https://doi.org/10.1016/j.tetasy.2004.09.011openalex-snapshot
Facile synthesis of C2-symmetric tridentate bis(thiazoline) and bis(oxazoline) ligands and their application in the enantioselective Henry reaction
inferredcites →https://doi.org/10.1021/ic051215iopenalex-snapshot
NH/π Interaction in a Spin-Crossover Complex [FeII(HLMe)2](BPh4)2·2CH3CN (BPh4- = Tetraphenylborate; HLMe = 2-Methylimidazol-4-yl-methylideneamino-2-ethylpyridine)
inferredcites →https://doi.org/10.1021/jo0262558openalex-snapshot
Coupling of Bulky, Electron-Deficient Partners in Aryl Amination in the Preparation of Tridentate Bis(oxazoline) Ligands for Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/jo050097dopenalex-snapshot
Asymmetric Henry Reaction Catalyzed by C2-Symmetric Tridentate Bis(oxazoline) and Bis(thiazoline) Complexes: Metal-Controlled Reversal of Enantioselectivity
inferredcites →https://doi.org/10.1021/jo0516537openalex-snapshot
Asymmetric Friedel−Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)−Bisoxazoline Complexes
inferredcites →https://doi.org/10.1039/b505220copenalex-snapshot
Enantioselective Friedel–Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst – synthesis of optically active tetrahydro-β-carbolines
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.4868679openalex-extracted
Enantioselective Friedel-Crafts Alkylation of 1,3,5-Trimethoxybenzene with Trans-Β-Nitrostyrenes Catalysed by [Cp*Rh{(R)-Prophos}(H2o)][Sbf6]2 (Prophos = Propane-1,2-Diyl-Bis(Diphenylphosphane)
inferred← citeshttps://doi.org/10.1002/047084289x.rz023.pub2openalex-snapshot
Zinc Trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1002/9780470066911.ch8openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/9780470669587.ch6openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/9783527675944.ch4openalex-snapshot
Zinc‐Catalyzed Friedel–Crafts Reactions
inferred← citeshttps://doi.org/10.1002/9783527675944.ch6openalex-snapshot
Zinc‐Catalyzed CC Bond Formation
inferred← citeshttps://doi.org/10.1002/9783527828166.ch5openalex-snapshot
Aromatic Electrophilic Substitution Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200600495openalex-snapshot
Asymmetric Friedel–Crafts Alkylations of Indoles with Ethyl Glyoxylate Catalyzed by (S)‐BINOL‐Titanium(IV) Complex: Direct Access to Enantiomerically Enriched 3‐Indolyl(hydroxy)acetates
inferred← citeshttps://doi.org/10.1002/adsc.200800523openalex-snapshot
Highly Enantioselective Friedel–Crafts Reaction of 4,7‐Dihydroindoles with β,γ‐Unsaturated α‐Keto Esters by Chiral Brønsted Acids
inferred← citeshttps://doi.org/10.1002/adsc.200900669openalex-snapshot
Highly Enantioselective Friedel–Crafts Reaction of Indole with Alkylidenemalonates Catalyzed by Heteroarylidene Malonate‐Derived Bis(oxazoline) Copper(II) Complexes
inferred← citeshttps://doi.org/10.1002/adsc.201000111openalex-snapshot
Development of Diphenylamine‐Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/adsc.201200547openalex-snapshot
Zinc‐Catalyzed Organic Synthesis: CC, CN, CO Bond Formation Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201500744openalex-snapshot
A Combination of Metal and Organic Catalysis: Highly Diastereo‐ and Enantioselective Construction of Fluorinated 2‐Aminocyclopenta[b]pyran Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201701557openalex-snapshot
Zinc‐Catalyzed Enantioselective Dearomative [3+2] Cycloaddition Reaction of 3‐Nitrobenzothiophenes and 3‐Nitrothieno[2,3‐b]yridine with 3‐Isothiocyanato Oxindoles
inferred← citeshttps://doi.org/10.1002/adsc.201800266openalex-snapshot
Zn‐Catalyzed Diastereo‐ and Enantioselective Dearomative [3+2] Cycloaddition Reaction of 2‐Nitroindoles and 2‐Nitrobenzothiophenes
inferred← citeshttps://doi.org/10.1002/ajoc.201700491openalex-snapshot
Recent Developments and Perspectives in the Zinc‐Catalysed Michael Addition
inferred← citeshttps://doi.org/10.1002/ange.200604263openalex-snapshot
Pd‐Catalyzed Cleavage of Benzylic Nitro Bonds: New Opportunities for Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/ange.200800770openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes: Cooperative Effect of 3 Å Molecular Sieves
inferred← citeshttps://doi.org/10.1002/ange.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.201001484openalex-snapshot
Orthogonal Enantioselectivity Approaches Using Homogeneous and Heterogeneous Catalyst Systems: Friedel–Crafts Alkylation of Indole
inferred← citeshttps://doi.org/10.1002/anie.200604263openalex-snapshot
Pd‐Catalyzed Cleavage of Benzylic Nitro Bonds: New Opportunities for Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200800770openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes: Cooperative Effect of 3 Å Molecular Sieves
inferred← citeshttps://doi.org/10.1002/anie.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201001484openalex-snapshot
Orthogonal Enantioselectivity Approaches Using Homogeneous and Heterogeneous Catalyst Systems: Friedel–Crafts Alkylation of Indole
inferred← citeshttps://doi.org/10.1002/asia.200800071openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Electron‐Rich N‐Heterocycles with Nitroalkenes Catalyzed by Diphenylamine‐Tethered Bis(oxazoline) and Bis(thiazoline) ZnII Complexes
inferred← citeshttps://doi.org/10.1002/asia.201000596openalex-snapshot
DFT Study of Chiral‐Phosphoric‐Acid‐Catalyzed Enantioselective Friedel–Crafts Reaction of Indole with Nitroalkene: Bifunctionality and Substituent Effect of Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/asia.201100820openalex-snapshot
Enantioselective [4+2] Cycloadditions of 2‐Vinyl‐1 H‐indoles with 3‐Nitro‐2 H‐chromenes Catalyzed by a Zn(OTf)2/Bis(oxazoline) Complex: An Efficient Approach to Fused Heterocycles with a Quaternary Stereocenter
inferred← citeshttps://doi.org/10.1002/asia.201900823openalex-snapshot
Potential Utilization of Metal–Organic Frameworks in Heterogeneous Catalysis: A Case Study of Hydrogen‐Bond Donating and Single‐Site Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.201601583openalex-snapshot
Friedel–Crafts Alkylation of Indoles with Nitroalkenes through Hydrogen‐Bond‐Donating Metal–Organic Framework
inferred← citeshttps://doi.org/10.1002/cctc.201800369openalex-snapshot
2D‐2D Nanocomposite of MoS2‐Graphitic Carbon Nitride as Multifunctional Catalyst for Sustainable Synthesis of C3‐Functionalized Indoles
inferred← citeshttps://doi.org/10.1002/cctc.202501060openalex-snapshot
Exploring the Role of Halogen Bond Donors in the Thiourea‐Catalyzed Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1002/chem.200700676openalex-snapshot
Superelectrophilicity of the Nitroolefinic Fragment of 4‐Nitrobenzodifuroxan in Michael‐Type Reactions with Indoles: A Kinetic Study in Acetonitrile
inferred← citeshttps://doi.org/10.1002/chem.200701439openalex-snapshot
A Library of Chiral Imidazoline–Aminophenol Ligands: Discovery of an Efficient Reaction Sphere
inferred← citeshttps://doi.org/10.1002/chem.200701908openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Indoles with Methyl (E)‐2‐Oxo‐4‐aryl‐3‐butenoates Catalyzed by Sc(OTf)3/pybox
inferred← citeshttps://doi.org/10.1002/chem.200800263openalex-snapshot
Highly Enantioselective Friedel–Crafts Reaction of 4,7‐Dihydroindoles with Imines by Chiral Phosphoric Acids: Facile Access to 2‐Indolyl Methanamine Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200802210openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Indoles with Alkylidene Malonates Catalyzed by N,N′‐Dioxide–Scandium(III) Complexes: Asymmetric Synthesis of β‐Carbolines
inferred← citeshttps://doi.org/10.1002/chem.200900033openalex-snapshot
Asymmetric Friedel–Crafts Reaction of 4,7‐Dihydroindoles with Nitroolefins by Chiral Brønsted Acids under Low Catalyst Loading
inferred← citeshttps://doi.org/10.1002/chem.200901635openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of 4,7‐Dihydroindoles with Enones Catalyzed by Primary–Secondary Diamines
inferred← citeshttps://doi.org/10.1002/chem.200903118openalex-snapshot
Iron‐ and Cobalt‐Catalyzed Asymmetric Hydrosilylation of Ketones and Enones with Bis(oxazolinylphenyl)amine Ligands
inferred← citeshttps://doi.org/10.1002/chem.201000540openalex-snapshot
Monodentate N‐Ligand‐Directed Bifunctional Transition‐Metal Catalysis: Highly Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/chem.201100479openalex-snapshot
Enantioselective Intramolecular Crossed Rauhut–Currier Reactions through Cooperative Nucleophilic Activation and Hydrogen‐Bonding Catalysis: Scope and Mechanistic Insight
inferred← citeshttps://doi.org/10.1002/chem.201303583openalex-snapshot
Enantioselective Cascade Michael Addition/Cyclization Reactions of 3‐Nitro‐2H‐Chromenes with 3‐Isothiocyanato Oxindoles: Efficient Synthesis of Functionalized Polycyclic Spirooxindoles
inferred← citeshttps://doi.org/10.1002/chem.201601301openalex-snapshot
Temperature Dual Enantioselective Control in a Rhodium‐Catalyzed Michael‐Type Friedel–Crafts Reaction: A Mechanistic Explanation
inferred← citeshttps://doi.org/10.1002/chin.200637113openalex-snapshot
Enantioselective Friedel—Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)—Zn(II) Complex.
inferred← citeshttps://doi.org/10.1002/cjoc.200790190openalex-snapshot
An Efficient Synthetic Method to Nonnatural α‐ and β‐Tryptophan Analogues via Friedel‐Crafts Alkylation of Indoles with Nitroacrylates
inferred← citeshttps://doi.org/10.1002/cjoc.201090243openalex-snapshot
Synthesis of Tridentate Ligands Based on Chiral Diamines and Their Application to Enantioselective Friedel‐Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/cjoc.201180480openalex-snapshot
Friedel‐Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Zn(II)‐Thiourea Complex
inferred← citeshttps://doi.org/10.1002/ejoc.200600646openalex-snapshot
Enantioselective Michael‐Type Friedel–Crafts Reactions of Indoles to Enones Catalyzed by a Chiral Camphor‐Based Brønsted Acid
inferred← citeshttps://doi.org/10.1002/ejoc.200900683openalex-snapshot
New Thiazoline–Oxazoline Ligands and Their Application in the Asymmetric Friedel–Crafts Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.200901434openalex-snapshot
Immobilization of Diphenylamine‐Linked Bis(oxazoline) Ligands and Their Application in the Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201001347openalex-snapshot
Synthesis and Application of Diphenyl Sulfide Linked Bis(imidazoline) Ligands: Dramatic Electronic Effect of Ligands on Catalytic Behavior
inferred← citeshttps://doi.org/10.1002/ejoc.201001587openalex-snapshot
Highly Enantioselective Henry Reaction Catalyzed by C2‐Symmetric Modular BINOL‐Oxazoline Schiff Base Copper(II) Complexes Generated in Situ
inferred← citeshttps://doi.org/10.1002/ejoc.201100683openalex-snapshot
The Asymmetric Friedel–Crafts Reaction of Indoles with Fluoroalkylated Nitroalkenes Catalyzed by Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/ejoc.201101335openalex-snapshot
Synthesis of Thiazoline–Oxazoline Ligands and Their Application in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201101648openalex-snapshot
Rhodium‐Catalyzed Asymmetric Addition of Arylboronic Acids to Indolylnitroalkenes
inferred← citeshttps://doi.org/10.1002/ejoc.201200382openalex-snapshot
Asymmetric Friedel–Crafts Alkylation of Indoles with Nitrodienes and 2‐Propargyloxy‐β‐nitrostyrenes Catalyzed by Diphenylamine‐Linked Bis(oxazoline)–Zn(OTf)2 Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201200584openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of N‐Methylindoles with Nitroalkenes Catalyzed by Chiral Bifunctional Abietic‐Acid‐Derived Thiourea‐ZnII Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201201636openalex-snapshot
Enantioselective Friedel–Crafts Alkylation of Indoles with (E)‐1‐Aryl‐4‐benzyloxybut‐2‐en‐1‐ones Catalyzed by an (R)‐3,3′‐Br2BINOLate–Hafnium(IV) Complex
inferred← citeshttps://doi.org/10.1002/ejoc.201300369openalex-snapshot
Leaving Group and Regioselectivity Switches in the Aminoalkylation Reaction of Indoles and Related Heterocycles with α‐Amido Sulfones
inferred← citeshttps://doi.org/10.1002/ejoc.201701480openalex-snapshot
Application of a One‐Pot Friedel–Crafts Alkylation/Michael Addition Methodology to the Asymmetric Synthesis of Ergoline Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202501247openalex-snapshot
Design and Synthesis of Lactose‐Derived Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation
inferred← citeshttps://doi.org/10.1002/jhet.569openalex-snapshot
An efficient and clean Michael addition of indoles to electron‐deficient olefins under solvent‐ and catalyst‐free condition
inferred← citeshttps://doi.org/10.1002/poc.1469openalex-snapshot
A theoretical and experimental study of the polar Diels–Alder cycloaddition of cyclopentadiene with nitrobenzodifuroxan
inferred← citeshttps://doi.org/10.1007/3418_2011_4openalex-snapshot
Bifunctional Acid Catalysts for Organic Synthesis
inferred← citeshttps://doi.org/10.1007/3418_2015_114openalex-snapshot
New Chemistry with Anionic NNN Pincer Ligands
inferred← citeshttps://doi.org/10.1007/7081_2007_073openalex-snapshot
Functionalization of Indole and Pyrrole Cores via Michael-Type Additions
inferred← citeshttps://doi.org/10.1007/7081_2010_52openalex-snapshot
Electrophilic Substitution Reactions of Indoles
inferred← citeshttps://doi.org/10.1007/s10562-014-1228-2openalex-snapshot
Chiral Bis(Oxazolinyl)thiophenes for Enantioselective Cu(II)-Catalyzed Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes
inferred← citeshttps://doi.org/10.1007/s10593-014-1514-3openalex-snapshot
Arenes and Hetarenes in Reactions with unsaturated Nitro Compounds (Review)
inferred← citeshttps://doi.org/10.1007/s11426-009-0179-8openalex-snapshot
Modification of diphenylamine-linked bis(oxazoline) ligands: Tuning of electronic effect and rigidity of ligand skeleton
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00406-7openalex-snapshot
4.04 Metal-Catalyzed Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1016/j.apcata.2011.03.010openalex-snapshot
Immobilization of 1,5,7-triazabicyclo [4.4.0] dec-5-ene over mesoporous materials: An efficient catalyst for Michael-addition reactions under solvent-free condition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.03.063openalex-snapshot
Modular synthesis of new C-aryl-nucleosides and their anti-CML activity
inferred← citeshttps://doi.org/10.1016/j.cclet.2008.06.032openalex-snapshot
Ytterbium triflate hydrate catalyzed Michael addition and cyclocondensation of α,β-unsaturated ketones with active methylene compounds
inferred← citeshttps://doi.org/10.1016/j.cclet.2011.04.013openalex-snapshot
Friedel–Crafts alkylation of indoles with nitroalkenes catalyzed by Cu(II)–imine complex
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.06.023openalex-snapshot
Enantioselective chlorination of β-keto esters and amides catalyzed by chiral copper(II) complexes of squaramide-linked bisoxazoline ligand
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.04.039openalex-snapshot
Synthesis, structural characterization of benzimidazole-functionalized Ni(II) and Hg(II) N-heterocyclic carbene complexes and their applications as efficient catalysts for Friedel–Crafts alkylations
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.10.011openalex-snapshot
Organometal-catalyzed asymmetric Friedel-Crafts reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123377openalex-snapshot
Enantioselective Friedel-Crafts alkylation of 1,3,5-trimethoxybenzene with trans-β-nitrostyrenes catalysed by [Cp*Rh{(R)-Prophos}(H2O)][SbF6]2 (Prophos = propane-1,2-diyl-bis(diphenylphosphane)
inferred← citeshttps://doi.org/10.1016/j.tet.2007.03.175openalex-snapshot
Catalytic and asymmetric Friedel–Crafts alkylation of indoles with nitroacrylates. Application to the synthesis of tryptophan analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2008.09.023openalex-snapshot
Cu(OTf)2/trisoxazoline catalyzed asymmetric Friedel–Crafts reaction of pyrroles with alkylidene malonates
inferred← citeshttps://doi.org/10.1016/j.tet.2008.11.083openalex-snapshot
Synthesis of 9,9′-biphenanthryl-10,10′-bis(oxazoline)s and their preliminary evaluations in the Friedel–Crafts alkylations of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2008.12.061openalex-snapshot
Enantioselective synthesis of (3-indolyl)glycine derivatives via asymmetric Friedel–Crafts reaction between indoles and glyoxylate imines
inferred← citeshttps://doi.org/10.1016/j.tet.2009.06.071openalex-snapshot
Trisoxazoline/Cu(II)-catalyzed asymmetric intramolecular Friedel–Crafts alkylation reaction of indoles
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.054openalex-snapshot
Asymmetric Friedel–Crafts alkylation of activated benzenes with methyl (E)-2-oxo-4-aryl-3-butenoates catalyzed by [Pybox/Sc(OTf)3]
inferred← citeshttps://doi.org/10.1016/j.tet.2011.11.047openalex-snapshot
Employing lactams for the unprecedented enantiopure synthesis of non-natural amino acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2012.02.078openalex-snapshot
The synthesis of phosphine oxide-linked bis(oxazoline) ligands and their application in asymmetric allylic alkylation
inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.068openalex-snapshot
Conformational change in a urea catalyst induced by sodium cation and its effect on enantioselectivity of a Friedel-Crafts reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2018.07.011openalex-snapshot
Critical view on the recent enantioselective synthesis of alcohols, amines and related molecules having tertiary benzylic stereocenter
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.04.037openalex-snapshot
BINAM and H8-BINAM-based chiral imines and Zn(OTf)2-catalyzed enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.02.057openalex-snapshot
Diphenylamine-derived bis-hydroxyamide catalyzed asymmetric borane reduction of prochiral ketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.01.015openalex-snapshot
Rational tuning of the rigidity of a ligand scaffold: synthesis of diphenylsulfide-linked bis(oxazoline) ligands and their application in asymmetric allylic alkylation
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.05.003openalex-snapshot
Enantioselective Friedel–Crafts alkylations catalysed by well-defined iridium and rhodium half-sandwich complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.11.018openalex-snapshot
Highly enantioselective Friedel–Crafts alkylation of indole with electron deficient trans-β-nitroalkenes using Zn(II)–oxazoline–imidazoline catalysts
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.05.011openalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with β,γ-unsaturated α-ketoesters catalyzed by new squaramide-linked bisoxazoline–Zn(OTf)2 complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.01.004openalex-snapshot
Highly enantioselective catalytic Friedel–Crafts reactions of cyclic α-alkylidene β-oxo imides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.12.081openalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes catalyzed by a bis(oxazoline)–Cu(II) complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.12.093openalex-snapshot
Convenient synthesis of bis(indolyl)alkanes and bis(pyrrolyl)alkanes by Cu(OTf)2-catalyzed addition of indole and pyrrole to acetylenic sulfone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.064openalex-snapshot
A highly efficient route to C-3 alkyl-substituted indoles via a metal-free transfer hydrogenation
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2010.09.007openalex-snapshot
An efficient synthesis of 3-substituted indole derivates under ultrasound irradiation
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80008-6openalex-snapshot
Chapter 5.2 Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80011-6openalex-snapshot
Chapter 5.5 Five-membered ring systems: with N and S (Se) atoms
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80013-xopenalex-snapshot
Chapter 5.7 Five-membered ring systems with O & N atoms
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70036-4openalex-snapshot
Chapter 5.5: Five-Membered Ring Systems: With N and S (Se) Atoms
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01767openalex-snapshot
Synthesis of Bis(oxazoline) Ligands Possessing C-5 gem -Disubstitution and Their Application in Asymmetric Friedel–Crafts Alkylations
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00123openalex-snapshot
Enantioselective Friedel–Crafts Alkylation Reactions of 3-Substituted Indoles with Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00612openalex-snapshot
Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01741openalex-snapshot
Electrostatically Enhanced Phosphoric Acids and Their Applications in Asymmetric Friedel–Crafts Alkylations
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02489openalex-snapshot
Zn-Catalyzed Diastereo- and Enantioselective Cascade Reaction of 3-Isothiocyanato Oxindoles and 3-Nitroindoles: Stereocontrolled Syntheses of Polycyclic Spirooxindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03584openalex-snapshot
Catalytic Asymmetric Synthesis of Chiral 2-Vinylindole Scaffolds by Friedel–Crafts Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03667openalex-snapshot
Diastereo- and Enantioselective Dearomative [3 + 2] Cycloaddition Reaction of 2-Nitrobenzofurans with 3-Isothiocyanato Oxindoles
inferred← citeshttps://doi.org/10.1021/acsomega.0c03485openalex-snapshot
Catalytic Enantioselective Alkylation of Indoles with trans -4-Methylthio-β-Nitrostyrene
inferred← citeshttps://doi.org/10.1021/ar5002457openalex-snapshot
Anionic Chiral Tridentate N-Donor Pincer Ligands in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/cr078372eopenalex-snapshot
Catalytic Asymmetric Friedel−Crafts Alkylation Reactions—Copper Showed the Way
inferred← citeshttps://doi.org/10.1021/cr400676vopenalex-snapshot
Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds
inferred← citeshttps://doi.org/10.1021/cr800189zopenalex-snapshot
Overview of the Chemistry of 2-Thiazolines
inferred← citeshttps://doi.org/10.1021/cr800400zopenalex-snapshot
Recent Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/ja400650mopenalex-snapshot
Highly Enantioselective Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters via Nickel-Catalyzed Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1021/ja8063292openalex-snapshot
Catalytic Enantioselective Additions of Indoles to Nitroalkenes
inferred← citeshttps://doi.org/10.1021/jacs.5b00033openalex-snapshot
Zn-Catalyzed Enantio- and Diastereoselective Formal [4 + 2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitro-Alkenes
inferred← citeshttps://doi.org/10.1021/jo102022gopenalex-snapshot
Asymmetric Michael Addition of 1-Acetylindolin-3-ones to β-Nitrostyrenes Catalyzed by Bifunctional Thioureas: A Simple Access to 2-Functionalized Indoles
inferred← citeshttps://doi.org/10.1021/jo200546aopenalex-snapshot
Catalytic Asymmetric Friedel–Crafts/Protonation of Nitroalkenes and N-Heteroaromatics
inferred← citeshttps://doi.org/10.1021/jo400747dopenalex-snapshot
Cu(OTf)2-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of Indoles with Arylidene Malonates Using Bis(sulfonamide)-Diamine Ligands
inferred← citeshttps://doi.org/10.1021/jo800529qopenalex-snapshot
TiCl4/Et3N-Promoted Three-Component Condensation between Aromatic Heterocycles, Aldehydes, and Active Methylene Compounds
inferred← citeshttps://doi.org/10.1021/jo801721zopenalex-snapshot
Second-Generation DBFOX Ligands for the Synthesis of β-Substituted α-Amino Acids via Enantioselective Radical Conjugate Additions
inferred← citeshttps://doi.org/10.1021/jo9013029openalex-snapshot
Chiral Bronsted Acid-Catalyzed Asymmetric Friedel−Crafts Alkylation of Pyrroles with Nitroolefins
inferred← citeshttps://doi.org/10.1021/jo9014613openalex-snapshot
InBr3: A Versatile Catalyst for the Different Types of Friedel−Crafts Reactions
inferred← citeshttps://doi.org/10.1021/ma4005549openalex-snapshot
Quasi-Living trans-1,4-Polymerization of Isoprene by Cationic Rare Earth Metal Alkyl Species Bearing a Chiral (S,S)-Bis(oxazolinylphenyl)amido Ligand
inferred← citeshttps://doi.org/10.1021/ol1025712openalex-snapshot
Chiral Brønsted Base-Promoted Nitroalkane Alkylation: Enantioselective Synthesis of sec-Alkyl-3-Substituted Indoles
inferred← citeshttps://doi.org/10.1021/ol201914ropenalex-snapshot
A New Type of Bis(sulfonamide)-Diamine Ligand for a Cu(OTf)2-Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/ol702003xopenalex-snapshot
Asymmetric Friedel−Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)−Zn(II) Complexes
inferred← citeshttps://doi.org/10.1021/ol800409dopenalex-snapshot
Ir-Catalyzed Regio- and Enantioselective Friedel–Crafts-Type Allylic Alkylation of Indoles
inferred← citeshttps://doi.org/10.1021/ol800945eopenalex-snapshot
Organocatalytic Highly Enantioselective Michael Addition of 2-Hydroxy-1,4-naphthoquinones to Nitroalkenes
inferred← citeshttps://doi.org/10.1021/ol8016929openalex-snapshot
Highly Enantioselective Friedel−Crafts Reaction of Indoles with 2-EnoylPyridine 1-Oxides Catalyzed by Chiral Pyridine 2,6-Bis(5′,5′-diphenyloxazoline)−Cu(II) Complexes
inferred← citeshttps://doi.org/10.1021/ol802838vopenalex-snapshot
PtCl4-Catalyzed Cyclization Reaction of β-Allenols in the Presence of Indoles
inferred← citeshttps://doi.org/10.1021/ol900461vopenalex-snapshot
Organocatalytic Enantioselective Friedel−Crafts Alkylation of 4,7-Dihydroindoles with α,β-Unsaturated Aldehydes: An Easy Access to 2-Substituted Indoles
inferred← citeshttps://doi.org/10.1021/om0602714openalex-snapshot
Modular Synthesis of a New Class of Bis(amino-oxazoline) Using Palladium-Catalyzed Buchwald−Hartwig Amination Methodology
inferred← citeshttps://doi.org/10.1021/om200714zopenalex-snapshot
A Cationic NCN Pincer Platinum(II) Aquo Complex with a Bis(imidazolinyl)phenyl Ligand: Studies toward its Synthesis and Asymmetric Friedel–Crafts Alkylation of Indoles with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/om401125qopenalex-snapshot
Metal–Nitroalkene and aci -Nitro Intermediates in Catalytic Enantioselective Friedel–Crafts Reactions of Indoles with trans -β-Nitrostyrenes
inferred← citeshttps://doi.org/10.1021/om5007616openalex-snapshot
Chiral Palladium(II) and Nickel(II) Complexes with C2-Symmetrical Tridentate Bis(oxazoline) Ligands: Synthesis, Characterization, and Catalytic Norbornene Polymerization
inferred← citeshttps://doi.org/10.1021/om801005jopenalex-snapshot
Chiral NCN Pincer Pt(II) and Pd(II) Complexes with 1,3-Bis(2′-imidazolinyl)benzene: Synthesis via Direct Metalation, Characterization, and Catalytic Activity in the Friedel−Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1038/s41598-023-41921-9openalex-snapshot
Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral Yb(OTf)3–pybox complex
inferred← citeshttps://doi.org/10.1039/b709283kopenalex-snapshot
Developments in asymmetric catalysis by metal complexes of chiral chelating nitrogen-donor ligands
inferred← citeshttps://doi.org/10.1039/b904275jopenalex-snapshot
Asymmetric Friedel–Crafts reaction of N-heterocycles and nitroalkenes catalyzed by imidazoline–aminophenol–Cu complex
inferred← citeshttps://doi.org/10.1039/b923835bopenalex-snapshot
Efficient in situ three-component formation of chiral oxazoline-Schiff base copper(ii) complexes: towards combinatorial library of chiral catalysts for asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1039/c000862aopenalex-snapshot
Enantioselective Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated acyl phosphonates catalyzed by chiral phosphoric acid
inferred← citeshttps://doi.org/10.1039/c2ob25315aopenalex-snapshot
Enantioselective Friedel–Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(ii) complex
inferred← citeshttps://doi.org/10.1039/c2ob25360gopenalex-snapshot
Asymmetric Friedel–Crafts alkylation of indoles with 3-nitro-2H-chromenes catalyzed by diphenylamine-linked bis(oxazoline) and bis(thiazoline) Zn(II) complexes
inferred← citeshttps://doi.org/10.1039/c3sc53542hopenalex-snapshot
Stereoselective construction of all-carbon quaternary center by means of chiral phosphoric acid: highly enantioselective Friedel–Crafts reaction of indoles with β,β-disubstituted nitroalkenes
inferred← citeshttps://doi.org/10.1039/c4cy01456aopenalex-snapshot
Synthesis of a chiral fluorescence active probe and its application as an efficient catalyst in the asymmetric Friedel–Crafts alkylation of indole derivatives with nitroalkenes
inferred← citeshttps://doi.org/10.1039/c8ob01943fopenalex-snapshot
Asymmetric fluorination of indanone-2-carboxylates using a polystyrene-supported diphenylamine-linked bis(oxazoline) complex
inferred← citeshttps://doi.org/10.1039/c9ob00545eopenalex-snapshot
A chiral bicyclic skeleton-tethered bipyridine–Zn(OTf) 2 complex as a Lewis acid: enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes
inferred← citeshttps://doi.org/10.1039/c9ra09227gopenalex-snapshot
Rose bengal as photocatalyst: visible light-mediated Friedel–Crafts alkylation of indoles with nitroalkenes in water
inferred← citeshttps://doi.org/10.1039/d0cc00693aopenalex-snapshot
Synthesis of chiral [2,3]-fused indolines through enantioselective dearomatization inverse-electron-demand Diels–Alder reaction/oxidation of indoles with 2-(2-nitrovinyl)-1,4-benzoquinone
inferred← citeshttps://doi.org/10.1039/d0nj04626dopenalex-snapshot
A robust heterogeneous Co-MOF catalyst in azide–alkyne cycloaddition and Friedel–Crafts reactions as well as hydrosilylation of alkynes
inferred← citeshttps://doi.org/10.1039/d1qo00369kopenalex-snapshot
Dinuclear helicate or mononuclear pincer lanthanide complexes from one ligand: stereo-controlled assembly and catalysis
inferred← citeshttps://doi.org/10.1039/d3ra06444aopenalex-snapshot
Recent advances in the synthesis and utility of thiazoline and its derivatives
inferred← citeshttps://doi.org/10.1039/d4qo00248bopenalex-snapshot
Naphthyridine–2NO, a new C 2 -symmetric rigid tetradentate bimetallic ligand and its application in asymmetric Friedel–Crafts alkylation
inferred← citeshttps://doi.org/10.1039/d5ra00456jopenalex-snapshot
Saccharide success: exploring the role of d -fructose-based thioureas as organocatalysts for the enantioselective Friedel–Crafts alkylation reaction
inferred← citeshttps://doi.org/10.1039/d6cc00711bopenalex-snapshot
Mantis-shaped bifunctional tridentate HoMPy-PI-NO ligands capable of cooperatively activating nucleophiles and electrophiles: empowering asymmetric addition reactions
inferred← citeshttps://doi.org/10.1055/b-0035-128263openalex-snapshot
10.13 Product Class 13: Indole and Its Derivatives
inferred← citeshttps://doi.org/10.1055/sos-sd-103-00147openalex-snapshot
3.1.11 Organometallic Complexes of Zinc (Update 2014)
inferred← citeshttps://doi.org/10.1080/10426507.2010.536189openalex-snapshot
Chiral Phosphoric Acid Catalyzed Asymmetric Friedel–Crafts Alkylation of Indoles with Nitroolefins
inferred← citeshttps://doi.org/10.3390/catal6090140openalex-snapshot
Highly Efficient Tetranuclear ZnII2LnIII2 Catalysts for the Friedel–Crafts Alkylation of Indoles and Nitrostyrenes
inferred← citeshttps://doi.org/10.3390/molecules15128582openalex-snapshot
Synthesis of New C2- Symmetric Fluoren-9-ylidene Malonate Derived Bis(oxazoline) Ligands and Their Application in Friedel-Crafts Reactions
inferred← citeshttps://doi.org/10.3390/molecules30030459openalex-snapshot
Scandium(III)-Enlarged Salen Complex-Catalyzed Asymmetric Michael Addition of Indoles to Enones
inferred← citeshttps://doi.org/10.3762/bjoc.9.137openalex-snapshot
Catalytic asymmetric tandem Friedel–Crafts alkylation/Michael addition reaction for the synthesis of highly functionalized chromans
inferred← citeshttps://doi.org/10.3987/com-08-s(f)93openalex-snapshot
Asymmetric Lewis Acid Catalysis of Aluminum(Salalen) Complexes: Friedel-Crafts Reaction of Indole
inferred← citeshttps://doi.org/10.71267/mencom.7701openalex-snapshot
Asymmetric Friedel-Crafts alkylation of indoles with β-nitrostyrenes catalyzed by a chiral NII complex based on (S)-(2-aminomethyl)pyrrolidine and 3,5-di-tert-butylsalicylaldehyde
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.