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Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid
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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/adsc.201100111openalex-snapshot
Catalytic Non‐Enzymatic Kinetic Resolution
inferredcites →https://doi.org/10.1002/adsc.201100410openalex-snapshot
Organocatalytic Enantioselective Decarboxylative Addition of Malonic Acids Half Thioesters to Isatins
inferredcites →https://doi.org/10.1002/adsc.201300375openalex-snapshot
Recent Advances in Catalytic Asymmetric Decarboxylative Addition Reactions
inferredcites →https://doi.org/10.1002/ange.201306297openalex-snapshot
Organocatalytic Enantioselective Decarboxylative Aldol Reaction of Malonic Acid Half Thioesters with Aldehydes
inferredcites →https://doi.org/10.1002/anie.200501041openalex-snapshot
Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding
inferredcites →https://doi.org/10.1002/anie.200704093openalex-snapshot
Desymmetrization‐like Catalytic Enantioselective Fluorination of Malonates and Its Application to Pharmaceutically Attractive Molecules
inferredcites →https://doi.org/10.1002/anie.201306297openalex-snapshot
Organocatalytic Enantioselective Decarboxylative Aldol Reaction of Malonic Acid Half Thioesters with Aldehydes
inferredcites →https://doi.org/10.1002/chem.201200367openalex-snapshot
Enantioselective Synthesis of AG‐041R by using N‐Heteroarenesulfonyl Cinchona Alkaloid Amides as Organocatalysts
inferredcites →https://doi.org/10.1002/chem.201201874openalex-snapshot
Regioselectivity‐Reversed Asymmetric Aldol Reaction of 1,3‐Dicarbonyl Compounds
inferredcites →https://doi.org/10.1016/0306-3623(92)90327-gopenalex-snapshot
The polyketide metabolites
inferredcites →https://doi.org/10.1016/j.tet.2011.05.108openalex-snapshot
Cu(I)-catalyzed decarboxylative aldol-type and Mannich-type reactions for asymmetric construction of contiguous trisubstituted and quaternary stereocenters
inferredcites →https://doi.org/10.1016/j.tetlet.2003.12.089openalex-snapshot
Cu(II)-catalyzed enantioselective aldol condensation between malonic acid hemithioesters and aldehydes
inferredcites →https://doi.org/10.1016/j.tetlet.2013.07.116openalex-snapshot
Synthesis of a new urea derivative: a dual-functional organocatalyst for Knoevenagel condensation in water
inferredcites →https://doi.org/10.1016/s0031-9422(00)89220-1openalex-snapshot
(+)-5-Hydroxy-dioxindole-3-acetic acid, a synergist from rice bran of auxin-induced ethylene production in plant tissue
inferredcites →https://doi.org/10.1021/cr020037xopenalex-snapshot
Asymmetric Alcoholysis of Cyclic Anhydrides
inferredcites →https://doi.org/10.1021/cr040640aopenalex-snapshot
Enantioselective Enzymatic Desymmetrizations in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr100339aopenalex-snapshot
Update 1 of: C2-Symmetric Chiral Bis(oxazoline) Ligands in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/cs3007389openalex-snapshot
Comparison of Asymmetric Hydrogenations of Unsaturated Carboxylic Acids and Esters
inferredcites →https://doi.org/10.1021/ja051759jopenalex-snapshot
Catalytic Enantioselective Thioester Aldol Reactions That Are Compatible with Protic Functional Groups
inferredcites →https://doi.org/10.1021/ja0668825openalex-snapshot
Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand
inferredcites →https://doi.org/10.1021/ja0673682openalex-snapshot
Stereoelectronic Effects Dictate Mechanistic Dichotomy between Cu(II)-Catalyzed and Enzyme-Catalyzed Reactions of Malonic Acid Half Thioesters
inferredcites →https://doi.org/10.1021/jacs.5b04175openalex-snapshot
Chemoselective Boron-Catalyzed Nucleophilic Activation of Carboxylic Acids for Mannich-Type Reactions
inferredcites →https://doi.org/10.1021/jo502741zopenalex-snapshot
Ni-Catalyzed Highly Chemo-, Regio-, and Enantioselective Decarboxylative Aldol Reaction of β,γ-Unsaturated α-Ketoesters with β-Ketoacids
inferredcites →https://doi.org/10.1021/np3002833openalex-snapshot
Alkaloids from the Root of Isatis indigotica
inferredcites →https://doi.org/10.1021/np800064wopenalex-snapshot
Isolation, Structure Elucidation, and Synthesis of Cytotoxic Tryptanthrin Analogues from Phaius mishmensis
inferredcites →https://doi.org/10.1021/ol301855wopenalex-snapshot
Enantioselective Construction of 3-Hydroxy Oxindoles via Decarboxylative Addition of β-Ketoacids to Isatins
inferredcites →https://doi.org/10.1021/ol401709topenalex-snapshot
Total Synthesis of a Pyrroloindoloquinazoline Alkaloid
inferredcites →https://doi.org/10.1021/ol4018062openalex-snapshot
Aryne Insertion Reactions Leading to Bioactive Fused Quinazolinones: Diastereoselective Total Synthesis of Cruciferane
inferredcites →https://doi.org/10.1021/ol402104popenalex-snapshot
Amino Acid Salts Catalyzed Asymmetric Aldol Reaction of Tryptanthrin: A Straightforward Synthesis of Phaitanthrin A and Its Derivatives
inferredcites →https://doi.org/10.1021/ol501954ropenalex-snapshot
A Dual Arylboronic Acid–Aminothiourea Catalytic System for the Asymmetric Intramolecular Hetero-Michael Reaction of α,β-Unsaturated Carboxylic Acids
inferredcites →https://doi.org/10.1039/b301028gopenalex-snapshot
The biosynthesis, molecular genetics and enzymology of the polyketide-derived metabolites
inferredcites →https://doi.org/10.1039/c1cs15120gopenalex-snapshot
Recent advances in enantioselective organocatalyzed anhydride desymmetrization and its application to the synthesis of valuable enantiopure compounds
inferredcites →https://doi.org/10.1039/c2cc30949aopenalex-snapshot
Biomimetic catalytic enantioselective decarboxylative aldol reaction of β-ketoacids with trifluoromethyl ketones
inferredcites →https://doi.org/10.1039/c3ob42161aopenalex-snapshot
Catalytic enantioselective decarboxylative reactions using organocatalysts
inferredcites →https://doi.org/10.1039/ct9089300598openalex-snapshot
LIV.—A β-lactonic acid from acetone and malonic acid
inferredcites →https://doi.org/10.1271/bbb1961.40.2465openalex-snapshot
Possible metabolic intermediates from IAA to .BETA.-acid in rice bran.
inferredcites →https://doi.org/10.2174/9781608054756113040003openalex-snapshot
Asymmetric Synthesis of α-Unsubstituted β-Hydroxy Acids
inferredcites →https://doi.org/10.3390/ijms16023980openalex-snapshot
Isolation and Cytotoxicity Evaluation of the Chemical Constituents from Cephalantheropsis gracilis
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.4538199openalex-extracted
Synthetic Diversification of Tryptanthrin Through its C6-Hydrazone
inferred← citeshttps://doi.org/10.1002/adsc.201800876openalex-snapshot
Organocatalytic Decarboxylative Cyanomethylation of Difluoromethyl and Trifluoromethyl Ketones
inferred← citeshttps://doi.org/10.1002/adsc.202200750openalex-snapshot
Visible Light‐Induced Radical‐Radical Coupling: One‐Pot Synthesis of 6‐Benzyl‐6‐hydroxyindolo[2,1‐b]quinazolin‐12(6H)‐ones from Isatins and Potassium Benzyl Trifluoroborates
inferred← citeshttps://doi.org/10.1002/ange.201916129openalex-snapshot
Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α‐Fluorinated Ketones
inferred← citeshttps://doi.org/10.1002/anie.201916129openalex-snapshot
Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α‐Fluorinated Ketones
inferred← citeshttps://doi.org/10.1002/chem.202003510openalex-snapshot
Stereoselective Copper‐Catalyzed Direct Aldol Reaction of β, γ‐Unsaturated α‐Ketoesters with Coumaran‐3‐Ones
inferred← citeshttps://doi.org/10.1002/chin.201618028openalex-snapshot
ChemInform Abstract: Direct Catalytic Asymmetric Synthesis of β‐Hydroxy Acids from Malonic Acid.
inferred← citeshttps://doi.org/10.1002/ejoc.201700399openalex-snapshot
A Diamino Alcohol Catalyzed Enantioselective Crossed Aldol Reaction of Acetaldehyde with Isatins – A Concise Total Synthesis of Antitumor Agents
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.11.001openalex-snapshot
Synthesis of pyrimidine-containing alkaloids
inferred← citeshttps://doi.org/10.1016/j.tet.2018.06.015openalex-snapshot
Recent advances in the asymmetric catalytic synthesis of chiral 3-hydroxy and 3-aminooxindoles and derivatives: Medicinally relevant compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134124openalex-snapshot
Catalytic efficiency of primary β-amino alcohols and primary α-amino amides in enantioselective reactions of isatins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153725openalex-snapshot
Photoenolization/nucleophilic addition enables direct access to 3-alkyl-3-hydroxy-indolin-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154752openalex-snapshot
Synthetic diversification of tryptanthrin through its C6-hydrazone
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02403openalex-snapshot
Divergent Synthesis of Methylisatoid and Tryptanthrin Derivatives by Ph3P–I2-Mediated Reaction of Isatins with and without Alcohols
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02854openalex-snapshot
Asymmetric Construction of α-Substituted β-Hydroxy Lactones via Ni Catalyzed Decarboxylative Addition Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02749openalex-snapshot
Organocatalytic Enantioselective Mannich Reaction of Cyclic N -Sulfonyl Ketimines to Tryptanthrin-Derived Ketimines
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02239openalex-snapshot
Preparation of Quinazolinoquinazolinones via a Cascade Approach
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01315openalex-snapshot
Switching of Enantioselectivity in the Cu-Catalyzed Asymmetric Decarboxylative Aldol Reaction of Tryptanthrin with β-Keto Acids: An Unexpected Counteranion Effect
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02247openalex-snapshot
Synthesis of Thioureas, Thioamides, and Aza-Heterocycles via Dimethyl-Sulfoxide-Promoted Oxidative Condensation of Sulfur, Malonic Acids, and Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03203openalex-snapshot
A Biomimetic Synthesis of Phaitanthrin E Involving a Fragmentation of sp3 Carbon–Carbon Bond: Synthesis and Rearrangement of Phaitanthrin D to Phaitanthrin E
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03466openalex-snapshot
Amination/Cyclization Cascade by Acid-Catalyzed Activation of Indolenine for the One-Pot Synthesis of Phaitanthrin E
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00408openalex-snapshot
Synthesis of Chiral (hydro)Indoloquinazolinones via Enantioselective Copper-Catalyzed Borylative Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00220openalex-snapshot
Chiral-at-Metal Rh(III) Complex-Catalyzed Decarboxylative Michael Addition of β-Keto Acids with α,β-Unsaturated 2-Acyl Imidazoles or Pyridine
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01336openalex-snapshot
Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02297openalex-snapshot
Ni(II)-Catalyzed Enantioselective Synthesis of β-Hydroxy Esters with Carboxylate Assistance
inferred← citeshttps://doi.org/10.1021/acsami.6c03941openalex-snapshot
Elemental Sulfur-Based Scalable Synthesis of Functional Polythioureas and co -Polythioureas with Tunable Mechanical and Optical Properties
inferred← citeshttps://doi.org/10.1039/c7cs00824dopenalex-snapshot
Catalytic enantioselective aldol reactions
inferred← citeshttps://doi.org/10.1039/c7ob00796eopenalex-snapshot
Organocatalytic decarboxylative aldol reaction of β-ketoacids with α-ketophosphonates en route to the enantioselective synthesis of tertiary α-hydroxyphosphonates
inferred← citeshttps://doi.org/10.1039/c7ob00823fopenalex-snapshot
Efficient chiral 1 H NMR analysis of indoloquinazoline alkaloids phaitanthrin A, cephalanthrin-A and their analogues with a chiral phosphoric acid
inferred← citeshttps://doi.org/10.1039/c9ob01243eopenalex-snapshot
Stereoselective construction of deoxy-cruciferane alkaloids by NHC-catalyzed intramolecular annulation of homoenolate with quinazolinone
inferred← citeshttps://doi.org/10.1039/d0nj04395hopenalex-snapshot
Synthesis of 6-substituted indoloquinazolinones from arynes and 2-acyl-4-quinazolinones: a transition-metal free C–N and C–C bond formation strategy
inferred← citeshttps://doi.org/10.1039/d0ob02032jopenalex-snapshot
Yb(OTf) 3 catalyzed [1,3]-rearrangement of 3-alkenyl oxindoles
inferred← citeshttps://doi.org/10.1039/d2qo00280aopenalex-snapshot
Asymmetric synthesis of δ-substituted-β-keto esters and β-substituted ketones via carboxyl-assisted site- and enantio-selective addition reactions
inferred← citeshttps://doi.org/10.1039/d3cc02673fopenalex-snapshot
An efficient Selectfluor-mediated condensation of indoles and anthranilates for the synthesis of indoloquinazolinones
inferred← citeshttps://doi.org/10.1039/d3qo00961kopenalex-snapshot
Enantioselective synthesis of tryptanthrin derivatives enabled by an asymmetric aza-Friedel–Crafts reaction
inferred← citeshttps://doi.org/10.1039/d3qo02029kopenalex-snapshot
Stereoselective skeletal modification of tryptanthrins to install chiral piperidine-2-ones enabled by Brønsted acid catalysis
inferred← citeshttps://doi.org/10.1039/d3qo02125dopenalex-snapshot
Enantioselective [3 + 2] annulation of tryptanthrin-derived ketimines and 2-naphthols: access to polycyclic indolo[2,1- b ]quinazoline derivatives
inferred← citeshttps://doi.org/10.1055/a-1707-2924openalex-snapshot
Phosphonium-Mediated Synthesis of a New Class of Indoloquinazoline Derivatives Bearing a C-12 Aryloxy Ester or Spiro-γ-lactone
inferred← citeshttps://doi.org/10.1177/00368504261477972openalex-snapshot
Pyridine-mediated tandem Knoevenagel condensation-decarboxylation: Chemoselectivity, mechanistic rationale, and discovery of a novel Lead(II) fumarate coordination polymer
inferred← citeshttps://doi.org/10.2174/1385272824999200818181531openalex-snapshot
Recent Achievements in Nucleophilic Decarboxylative Addition Reactions
inferred← citeshttps://doi.org/10.3390/ijms24065101openalex-snapshot
Microwave-Assisted Synthesis of 3-Hydroxy-2-oxindoles and Pilot Evaluation of Their Antiglaucomic Activity
inferred← citeshttps://doi.org/10.3987/rev-18-sr(t)3openalex-snapshot
β-Amino Alcohol Organocatalysts for Asymmetric Additions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.76.802openalex-snapshot
Synthesis of Indoloquinazoline Alkaloids Using Cascade Reactions
inferred← citeshttps://doi.org/10.6023/cjoc202208036openalex-snapshot
Visible Light-Assisted Photocatalyst-Free Tandem Sulfonylation/ Cyclization for the Synthesis of Oxindoles
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