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Bismuth Nitrate-Catalyzed Versatile Michael Reactions

https://doi.org/10.1021/jo026550s
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What this work says

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

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Transition-Metal Catalysis of the Michael Reaction of 1,3-Dicarbonyl Compounds and Acceptor-Activated Alkenes
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Modern Variants of the Mannich Reaction
inferredcites →https://doi.org/10.1016/0040-4020(95)00446-fopenalex-snapshot
FeCl3-catalyzed conjugate addition of secondary amines, imidazole and pyrazole to methyl 2-acetamidoacrylate. Preparation of β-dialkylamino-αalanine and β-(N-heteroaryi)-α-alanine derivatives
inferredcites →https://doi.org/10.1016/0040-4039(88)80005-4openalex-snapshot
A simple conversion of [E]- into the isomeric [Z]-2-(1-substituted-1-alkenyl)-1,3,2-dioxaborinanes, providing a convenient stereospecific synthesis of both [E]- and [Z]-1,2-disubstituted vinyl bromides
inferredcites →https://doi.org/10.1016/s0040-4020(01)97970-0openalex-snapshot
Stereochemistry of aminocarbonyl compounds—X
inferredcites →https://doi.org/10.1016/s0040-4020(97)00325-6openalex-snapshot
Stereoselective synthesis of 2-aryloxy esters: An asymmetric approach to fluoxetine, tomoxetine and nisoxetine
inferredcites →https://doi.org/10.1016/s0040-4020(98)00791-1openalex-snapshot
Mukaiyama aldol and Michael reactions catalyzed by lanthanide iodides
inferredcites →https://doi.org/10.1016/s0040-4020(99)00358-0openalex-snapshot
Nickel(II)-catalyzed Michael additions. Formation of quaternary centers and diastereoselective addition of enantiopure N -acetoacetyl-4-benzyloxazolidin-2-one
inferredcites →https://doi.org/10.1016/s0040-4039(00)01126-6openalex-snapshot
Unprecedented stereoselectivity in the Staudinger reaction with polycyclic aromatic imines
inferredcites →https://doi.org/10.1016/s0040-4039(00)01397-6openalex-snapshot
Surface-mediated highly efficient regioselective nitration of aromatic compounds by bismuth nitrate
inferredcites →https://doi.org/10.1016/s0040-4039(00)86116-xopenalex-snapshot
Reactions on solid supports part IV: Reactions of αβ-unsaturated carbonyl compounds with indoles using clay as catalyst
inferredcites →https://doi.org/10.1016/s0040-4039(00)99297-9openalex-snapshot
Catalysis of the specific michael addition : The example of acrylate acceptors
inferredcites →https://doi.org/10.1016/s0040-4039(01)01697-5openalex-snapshot
Addition of pyrroles to electron deficient olefins employing InCl3
inferredcites →https://doi.org/10.1016/s0040-4039(02)02236-0openalex-snapshot
A new entry to N-unsubstituted β-lactams through a solid-phase approach
inferredcites →https://doi.org/10.1016/s0040-4039(98)01555-xopenalex-snapshot
A facile reduction of aromatic nitro compounds to aromatic amines by samarium and iodine
inferredcites →https://doi.org/10.1016/s0040-4039(98)02587-8openalex-snapshot
Rigid aminoalcohol backbone as a highly defined chiral template for the preparation of optically active tertiary α-hydroxyl acids
inferredcites →https://doi.org/10.1016/s0957-4166(97)00534-xopenalex-snapshot
New δ-aminoalcohol for the enantioselective addition of dialkylzincs to aldehydes
inferredcites →https://doi.org/10.1016/s0960-894x(98)00520-4openalex-snapshot
Polycyclic aromatic compounds as anticancer agents: Synthesis and biological evaluation of some chrysene derivatives
inferredcites →https://doi.org/10.1016/s0968-0896(00)00213-3openalex-snapshot
Polycyclic aromatic compounds as anticancer agents: synthesis and biological evaluation of dibenzofluorene derivatives
inferredcites →https://doi.org/10.1021/ja00387a060openalex-snapshot
Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric induction
inferredcites →https://doi.org/10.1021/ja01568a041openalex-snapshot
The Reaction of Substituted Indoles with Methyl Vinyl Ketone. New Synthesis of 2-Methylcarbazole
inferredcites →https://doi.org/10.1021/ja960766sopenalex-snapshot
A Novel Chiral Super-Lewis Acidic Catalyst for Enantioselective Synthesis
inferredcites →https://doi.org/10.1021/ja980520iopenalex-snapshot
Chiral Lewis Acid Catalysis in Conjugate Additions of O-Benzylhydroxylamine to Unsaturated Amides. Enantioselective Synthesis of β-Amino Acid Precursors
inferredcites →https://doi.org/10.1021/jm00013a020openalex-snapshot
[(Alkylamino)methyl]acrylophenones: Potent and Selective Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase
inferredcites →https://doi.org/10.1021/jo00097a039openalex-snapshot
Chemo- and Diastereoselective Reduction of .beta.-Enamino Esters: A Convenient Synthesis of Both cis- and trans-.gamma.-Amino Alcohols and .beta.-Amino Esters
inferredcites →https://doi.org/10.1021/jo00294a026openalex-snapshot
Highly stereoselective syntheses involving N-alkyl-4,4,7.alpha.-trimethyl-trans-octahydro-1,3-benzoxazine intermediates. 2.
inferredcites →https://doi.org/10.1021/jo0057497openalex-snapshot
Novel Sequential Process from N -Methoxyamides and Vinyl Grignard Reagents: New Synthesis of β-Aminoketones
inferredcites →https://doi.org/10.1021/jo01022a023openalex-snapshot
The Synthesis of β-Amino Mercaptans and β-Amino Thiosulfates via Ethylenimine Intermediates1
inferredcites →https://doi.org/10.1021/jo0108764openalex-snapshot
Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica Gel
inferredcites →https://doi.org/10.1021/jo016180sopenalex-snapshot
A Simple and Efficient Chemoselective Method for the Catalytic Deprotection of Acetals and Ketals Using Bismuth Triflate
inferredcites →https://doi.org/10.1021/jo0163243openalex-snapshot
Sequential One-Pot InBr3-Catalyzed 1,4- then 1,2-Nucleophilic Addition to Enones
inferredcites →https://doi.org/10.1021/jo025606fopenalex-snapshot
Reaction of Allylzinc Reagents and Zinc Enolates of Ketones with α-Amidoalkylphenyl Sulfones
inferredcites →https://doi.org/10.1021/ol006500eopenalex-snapshot
N-Benzylhydroxylamine Addition to β-Aryl Enoates. Enantioselective Synthesis of β-Aryl-β-amino Acid Precursors
inferredcites →https://doi.org/10.1021/ol0256163openalex-snapshot
Transition Metal Salts-Catalyzed Aza-Michael Reactions of Enones with Carbamates
inferredcites →https://doi.org/10.1021/ol9911122openalex-snapshot
Direct Synthesis of β-Aminoketones from Amides via Novel Sequential Nucleophilic Substitution/Michael Reaction
inferredcites →https://doi.org/10.1039/a803880eopenalex-snapshot
Brevicompanines A and B: new plant growth regulators produced by the fungus, Penicillium brevicompactum
inferredcites →https://doi.org/10.1039/b002833iopenalex-snapshot
Indium-mediated facile synthesis of 3-unsubstituted β-lactams
inferredcites →https://doi.org/10.1039/p19910002435openalex-snapshot
Stereoselective synthesis of sperabillins and related compounds
inferredcites →https://doi.org/10.1039/p19960002823openalex-snapshot
Asymmetric titanium-catalysed Michael addition of O-benzylhydroxylamine to αβ-unsaturated carbonyl compounds: synthesis of β-amino acid precursors
inferredcites →https://doi.org/10.1055/s-1995-5059openalex-snapshot
An Asymmetric Synthesis of N-Protected β-Amino Aldehydes and β-Amino Ketones
inferredcites →https://doi.org/10.1055/s-2001-18068openalex-snapshot
InCl3-Catalysed Conjugate Addition of Indoles with Electron-Deficient Olefins
inferredcites →https://doi.org/10.1080/00397910008086894openalex-snapshot
Sodium Bismuthate Mediated Oxidation of Allylic and Benzylic Alcohols
inferredcites →https://doi.org/10.1081/scc-120004840openalex-snapshot
BISMUTH NITRATE-MEDIATED DEPROTECTION OF OXIMES
inferredcites →https://doi.org/10.1139/cjc-76-9-1256openalex-snapshot
The ultra high pressure conjugate addition of indoles to electron-deficient olefins
inferredcites →https://doi.org/10.1358/dof.1997.022.09.423212openalex-snapshot
Atorvastatin Calcium
inferredcites →https://doi.org/10.3184/030823401103169199openalex-snapshot
Synthesis of Tricyclic β-Lactams via Palladium Acetate-Induced Heck Reaction
inferredcites →https://doi.org/10.3987/com-00-9019openalex-snapshot
Indium-mediated Facile Synthesis of 3-Unsubstituted Ferrocenyl b-Lactams
inferredcites →https://doi.org/10.3998/ark.5550190.0002.804openalex-snapshot
Montmorillonite impregnated with bismuth nitrate: A versatile reagent for the synthesis of nitro compounds of biological significance

What points at this work

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

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Cobalt(Ii) Catalyzed Michael-Type Hydroarylamination of Activated Olefins
inferred← citeshttps://doi.org/10.1002/047084289x.rn01215.pub2openalex-snapshot
(1R,1′R,2S,2′S)-2,2′-Bis(1,1-dimethylethyl)-2,2′,3,3′-tetrahydro-1,1′-bi-1H-isophosphindole and (1S,1′S,2R,2′R)-2,2′-Bis(1,1-dimethylethyl)-2,2′,3,3′-tetrahydro-1,1′-bi-1H-isophosphindole
inferred← citeshttps://doi.org/10.1002/047084289x.rn01657openalex-snapshot
Zinc(II) Perchlorate Hexahydrate
inferred← citeshttps://doi.org/10.1002/047084289x.rn01981openalex-snapshot
Bismuth(III) Nitrate Pentahydrate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos01293.pub2openalex-snapshot
Bismuth( III ) nitrate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos01293.pub3openalex-snapshot
Bismuth( III ) Nitrate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos01293.pub4openalex-snapshot
Bismuth( III ) nitrate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos01293.pub5openalex-snapshot
Bismuth( III ) nitrate
inferred← citeshttps://doi.org/10.1002/9781118662083.cot05-003openalex-snapshot
Formation of Amines from Alkenes, Dienes, and Alkynes
inferred← citeshttps://doi.org/10.1002/9781118662083.cot08-015openalex-snapshot
Formation of Aldehydes and Ketones by 1,4‐Addition to α,β‐Unsaturated Carbonyl Compounds and Derivatives
inferred← citeshttps://doi.org/10.1002/9783527619450.ch5openalex-snapshot
C‐H Transformation at Arenes
inferred← citeshttps://doi.org/10.1002/9783527637737.ch5openalex-snapshot
Five‐Membered Heterocycles: Indole and Related Systems
inferred← citeshttps://doi.org/10.1002/adsc.200404348openalex-snapshot
Micellar Solution of Sodium Dodecyl Sulfate (SDS) Catalyzes Facile Michael Addition of Amines and Thiols to α,β‐Unsaturated Ketones in Water under Neutral Conditions
inferred← citeshttps://doi.org/10.1002/adsc.200404361openalex-snapshot
Cu(acac)2 Immobilized in Ionic Liquids: A Recoverable and Reusable Catalytic System for Aza‐Michael 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.201100155openalex-snapshot
Bismuth(III) Triflate‐Based Catalytic Direct Opening of Oleanolic Hydroxy‐γ‐lactones to Afford 12‐Oxo‐28‐carboxylic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201300493openalex-snapshot
Iodine‐Catalyzed Selective Synthesis of 2‐Sulfanylphenols via Oxidative Aromatization of Cyclohexanones and Disulfides
inferred← citeshttps://doi.org/10.1002/adsc.201500502openalex-snapshot
Easy Access to a Library of Alkylindoles: Reductive Alkylation of Indoles with Carbonyl Compounds and Hydrosilanes under Indium Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.201901037openalex-snapshot
Alkylation of Indoles with α,β‐Unsaturated Ketones using Alumina in Hexanes
inferred← citeshttps://doi.org/10.1002/ajoc.201700609openalex-snapshot
Thia‐Michael Addition: An Emerging Strategy in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/ajoc.201800087openalex-snapshot
Sequential Ytterbium(III) Triflate Catalyzed One‐Pot Three‐Component Thia‐Michael Addition
inferred← citeshttps://doi.org/10.1002/ajoc.202000264openalex-snapshot
Ruthenium(II)‐catalyzed Monohydroalkylation of α,β‐Unsaturated Ketones with N‐Acyl Pyrroles using a C−H Activation Strategy
inferred← citeshttps://doi.org/10.1002/ajoc.202200440openalex-snapshot
A Simple and General Nickel‐Catalyzed Michael‐Type Hydroamination of Activated Olefins Using Arylamines
inferred← citeshttps://doi.org/10.1002/ange.200301679openalex-snapshot
Neue katalytische Methoden in der stereoselektiven Friedel‐Crafts‐Alkylierung
inferred← citeshttps://doi.org/10.1002/ange.201005296openalex-snapshot
Lewis Acid Catalyzed Intramolecular Direct Ene Reaction of Indoles
inferred← citeshttps://doi.org/10.1002/anie.200301679openalex-snapshot
New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
inferred← citeshttps://doi.org/10.1002/anie.201005296openalex-snapshot
Lewis Acid Catalyzed Intramolecular Direct Ene Reaction of Indoles
inferred← citeshttps://doi.org/10.1002/aoc.3171openalex-snapshot
Aminopropylated PEG as a novel, eco‐friendly and biodegradable basic catalyst for bis‐Michael addition to α,β‐unsaturated ketones under solvent‐free conditions
inferred← citeshttps://doi.org/10.1002/asia.200700410openalex-snapshot
Synthesis and Characterization of Silica@Copper Core–Shell Nanoparticles: Application for Conjugate Addition Reactions
inferred← citeshttps://doi.org/10.1002/asia.201402363openalex-snapshot
One‐Pot Consecutive Catalysis by Integrating Organometallic Catalysis with Organocatalysis
inferred← citeshttps://doi.org/10.1002/asia.201403312openalex-snapshot
Synthesis of Indole Terpenoid Mimics through a Functionality‐Tolerated Eu(fod)3‐Catalyzed Conjugate Addition
inferred← citeshttps://doi.org/10.1002/cctc.201402309openalex-snapshot
Selective N‐Alkylation of Indoles with α,β‐Unsaturated Compounds Catalyzed by a Monomeric Phosphate
inferred← citeshttps://doi.org/10.1002/chem.200305407openalex-snapshot
Evidence That Protons Can Be the Active Catalysts in Lewis Acid Mediated Hetero‐Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/chem.200500823openalex-snapshot
Multiple Component Approaches to C‐Glycosyl β‐Amino Acids by Complementary One‐Pot Mannich‐Type and Reformatsky‐Type Reactions
inferred← citeshttps://doi.org/10.1002/chem.200600415openalex-snapshot
Intramolecular Hetero‐Michael Addition of β‐Hydroxyenones for the Preparation of Highly Substituted Tetrahydropyranones
inferred← citeshttps://doi.org/10.1002/chem.200903508openalex-snapshot
A Three‐Component Reaction Based on a Remote‐Group‐Directed Dynamic Kinetic Aza‐Michael Addition: Stereoselective Synthesis of Imidazolidin‐4‐ones
inferred← citeshttps://doi.org/10.1002/chem.201100654openalex-snapshot
Regioselective Synthesis of β‐Aryl‐ and β‐Amino‐Substituted Aliphatic Esters by Rhodium‐Catalyzed Tandem Double‐Bond Migration/Conjugate Addition
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Bismuth Nitrate Catalyzed Versatile Michael Reactions.
inferred← citeshttps://doi.org/10.1002/cjoc.200790328openalex-snapshot
Conjugate Addition of Indoles to α,β‐Unsaturated Ketones (Chalcones) Catalyzed by KHSO4 under Ultrasonic Conditions
inferred← citeshttps://doi.org/10.1002/cjoc.200890238openalex-snapshot
Synthesis of β‐Amino Acids via Catalyst‐ and Solvent‐Free Aza‐Michael Reaction
inferred← citeshttps://doi.org/10.1002/cjoc.200890260openalex-snapshot
Solvent‐free Thia‐Michael Addition Reactions Using 3‐[Bis(alkylthio)methylene]pentane‐2,4‐diones as Efficient and Odorless Thiol Equivalents
inferred← citeshttps://doi.org/10.1002/cjoc.201180484openalex-snapshot
Potassium tert‐Butoxide Catalyzed Synthesis and Characterization of Novel 3‐Aryl‐3‐(phenylthio)‐1‐(thiophen‐3‐yl)propan‐1‐one Derivatives
inferred← citeshttps://doi.org/10.1002/cjoc.201190011openalex-snapshot
Highly Efficient InBr3 Catalyzed Michael Addition of Indoles to α,β‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/ejoc.200500400openalex-snapshot
A Highly Efficient Synthetic Protocol for Tetrahydropyranylation/Depyranylation of Alcohols and Phenols
inferred← citeshttps://doi.org/10.1002/ejoc.200600006openalex-snapshot
Perchloric Acid Impregnated on Silica Gel (HClO4/SiO2): A Versatile Catalyst for Michael Addition of Thiols to the Electron‐Deficient Alkenes
inferred← citeshttps://doi.org/10.1002/ejoc.200600390openalex-snapshot
An Efficient and Selective Hydroarylation of Styrenes with Electron‐Rich Arenes, Catalyzed by Bismuth(III) Chloride and Affording Markovnikov Adducts
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Borax as an Efficient Metal‐Free Catalyst for Hetero‐Michael Reactions in an Aqueous Medium
inferred← citeshttps://doi.org/10.1002/ejoc.201800780openalex-snapshot
Fe(OTf)2‐Catalyzed Thia‐Michael Addition Reaction: A Green Synthetic Approach to β‐Thioethers
inferred← citeshttps://doi.org/10.1002/hc.20352openalex-snapshot
Highly convenient one‐pot conversion of aryl acylals or aryl aldehyde bisulfites into dihydropyrimidones using BI(NO3)3⋅5H2O
inferred← citeshttps://doi.org/10.1002/hc.21112openalex-snapshot
Selected Reactions of Diethyl (E)‐1‐(bromomethyl)‐2‐cyanovinylphosphonate with Secondary and Tertiary Amines
inferred← citeshttps://doi.org/10.1002/hlca.200490139openalex-snapshot
Transition‐Metal‐Based Lewis Acid Catalysis of Aza‐Type Michael Additions of Amines to α,β‐Unsaturated Electrophiles in Water
inferred← citeshttps://doi.org/10.1002/hlca.201100202openalex-snapshot
A Novel Asymmetric Synthesis of 3‐(1 H ‐Pyrrol‐1‐yl)‐Substituted β ‐Lactams via a Bismuth Nitrate‐Catalyzed Reaction
inferred← citeshttps://doi.org/10.1002/jccs.201000180openalex-snapshot
Functionalized Ionic Liquid Promoted Aza‐Michael Addition of Aromatic Amines
inferred← citeshttps://doi.org/10.1002/jhet.4221openalex-snapshot
Aza‐Michael addition of 1, 2‐diazoles to structurally diverse enones: Efficient methods toward β‐amino ketones
inferred← citeshttps://doi.org/10.1002/jhet.5570450213openalex-snapshot
Synthesis of 3‐substituted indoles promoted by pulverization‐activation method catalyzed by Bi(NO3)3·5H2O
inferred← citeshttps://doi.org/10.1002/jhet.5570450650openalex-snapshot
N‐donor ligand as catalyst: A simple aza‐michael addition reaction in aqueous media
inferred← citeshttps://doi.org/10.1002/jhet.659openalex-snapshot
Synthesis and application of modified silica sulfuric acid as a solid acid heterogeneous catalyst in Michael addition reactions
inferred← citeshttps://doi.org/10.1002/marc.201000545openalex-snapshot
Improved Synthesis Strategy of Poly(amidoamine)s for Biomedical Applications: Catalysis by “Green” Biocompatible Earth Alkaline Metal Salts
inferred← citeshttps://doi.org/10.1002/qua.22028openalex-snapshot
Theoretical study of the Michael addition of acetylacetone to methyl vinyl ketone catalyzed by the ionic liquid 1‐butyl‐3‐methylimidazolium hydroxide
inferred← citeshttps://doi.org/10.1002/slct.201700265openalex-snapshot
Bismuth Nitrate Catalyzed One‐Pot Multicomponent Synthesis of a Novel Series of Diversely Substituted 1,8‐Dioxodecahydroacridines at Room Temperature #
inferred← citeshttps://doi.org/10.1002/slct.201902832openalex-snapshot
One‐Pot Three‐Component Synthesis of 3‐Aminoalkyl Indoles Catalyzed by Molecular Iodine
inferred← citeshttps://doi.org/10.1002/slct.201904851openalex-snapshot
Brönsted Acidic Ionic Liquids Catalysed Sequential Michael‐Like Addition of Indole with Chalcones via Claisen‐Schmidt Condensation
inferred← citeshttps://doi.org/10.1002/slct.202204860openalex-snapshot
Arene Diazonium Tetrafluoroborate Salts: Novel Lewis Acid Catalysts for Friedel‐Crafts Alkylation of Indoles with α,β‐Unsaturated Ketones
inferred← citeshttps://doi.org/10.1002/zaac.201900012openalex-snapshot
To Coordinate or not to Coordinate: The Special Role of Chalcogen Ether Functionalities in the Design of Twofold Functionalized Cyclopentadienyl Ligands [Cp,O,Ch (Ch = S, Se)]
inferred← citeshttps://doi.org/10.1007/128_2011_274openalex-snapshot
Bismuth(III) Salts as Synthetic Tools in Organic Transformations
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_28openalex-snapshot
Novel Anticancer β-Lactams
inferred← citeshttps://doi.org/10.1007/7081_2010_52openalex-snapshot
Electrophilic Substitution Reactions of Indoles
inferred← citeshttps://doi.org/10.1007/7081_2012_88openalex-snapshot
Synthesis of β-Lactams and Their Chemical Manipulations Via Microwave-Induced Reactions
inferred← citeshttps://doi.org/10.1007/s00706-007-0697-zopenalex-snapshot
Antimony(III) Sulfate Catalyzed Condensation Reaction of Indoles with Carbonyl Compounds
inferred← citeshttps://doi.org/10.1007/s00706-008-0064-8openalex-snapshot
A synthesis of diethyl alkylsulfanylmethylmalonates catalyzed by KOH in an ionic liquid
inferred← citeshttps://doi.org/10.1007/s00706-008-0886-4openalex-snapshot
Triethylammonium acetate (TEAA): a recyclable inexpensive ionic liquid promotes the chemoselective aza- and thia-Michael reactions
inferred← citeshttps://doi.org/10.1007/s00706-008-0917-1openalex-snapshot
Green protocol for conjugate addition of amines to p-quinones accelerated by water
inferred← citeshttps://doi.org/10.1007/s00706-011-0550-2openalex-snapshot
Cesium fluoride catalyzed Aza-Michael addition reaction in aqueous media
inferred← citeshttps://doi.org/10.1007/s00706-012-0729-1openalex-snapshot
K3PO4-catalyzed one-pot synthesis of β-amino ketones
inferred← citeshttps://doi.org/10.1007/s00706-016-1752-4openalex-snapshot
A green and convenient approach for the one-pot solvent-free synthesis of coumarins and β-amino carbonyl compounds using Lewis acid grafted sulfonated carbon@titania composite
inferred← citeshttps://doi.org/10.1007/s00894-023-05623-3openalex-snapshot
Evidences of noncovalent interactions between indole and dichloromethane under different solvent conditions
inferred← citeshttps://doi.org/10.1007/s10562-008-9646-7openalex-snapshot
An Efficient Protocol for Aza-Michael Addition Reactions Under Solvent-Free Condition Employing Sulfated Zirconia Catalyst
inferred← citeshttps://doi.org/10.1007/s10562-009-0157-yopenalex-snapshot
Phosphate Impregnated Titania: An Efficient Reusable Heterogeneous Catalyst for Aza-Michael Reactions Under Solvent-Free Condition
inferred← citeshttps://doi.org/10.1007/s10562-016-1743-4openalex-snapshot
Synthesis, Characterization and Catalytic Application of MCM 41 Supported Phenanthrolinium Dibromide Catalyst for Aza-Michael Addition Reaction in Aqueous Medium
inferred← citeshttps://doi.org/10.1007/s10562-018-2490-5openalex-snapshot
Synthesis and Catalytic Application of Mixed Valence Iron (FeII/FeIII)-Based OMS-MIL-100(Fe) as an Efficient Green Catalyst for the aza-Michael Reaction
inferred← citeshttps://doi.org/10.1007/s10562-020-03459-7openalex-snapshot
Heterogeneous Aza-Michael Addition Reaction by the Copper-Based Metal–Organic Framework (CuBTC)
inferred← citeshttps://doi.org/10.1007/s10870-013-0432-zopenalex-snapshot
Synthesis, Structural, and UV Studies of Two Uracil Derivatives, Methyl 3-(5-Fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propanoate and Methyl 3-(5-Chloro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)propanoate
inferred← citeshttps://doi.org/10.1007/s10904-021-02006-0openalex-snapshot
Catalytic Application of Ceric Ammonium Nitrate-Stabilized Maghemite Nanoparticles (CAN-γ-Fe2O3) for Ultrasound Assisted Synthesis of β-Amino Derivatives
inferred← citeshttps://doi.org/10.1007/s11030-009-9184-2openalex-snapshot
The Michael addition of indoles and pyrrole to α-, β-unsaturated ketones and double-conjugate 1,4-addition of indoles to symmetric enones promoted by pulverization-activation method and Thia-Michael addition catalyzed by wet cyanuric chloride
inferred← citeshttps://doi.org/10.1007/s11164-013-1139-7openalex-snapshot
Molecular iodine catalyzed coupling reactions of indole with 1,3-dicarbonyl compounds
inferred← citeshttps://doi.org/10.1007/s11164-013-1172-6openalex-snapshot
Rapid three-component synthesis of pyrimidine and pyrimidinone derivatives in the presence of Bi(NO3)3·5H2O as a mild and highly efficient catalyst
inferred← citeshttps://doi.org/10.1007/s11164-014-1703-9openalex-snapshot
Microwave-assisted Michael addition of 2-amino pyridine to chalcones under catalyst-free conditions
inferred← citeshttps://doi.org/10.1007/s11164-015-2208-xopenalex-snapshot
Synthesis, antioxidant and anticancer screenings of berberine–indole conjugates
inferred← citeshttps://doi.org/10.1007/s11164-025-05743-wopenalex-snapshot
Crushed 3 Å, 4 Å, and 5 Å molecular sieves: a green heterogeneous catalyst for solvent-free aza-Michael additions via microwave, ultrasound, and mechanochemical activation
inferred← citeshttps://doi.org/10.1007/s11434-010-3147-yopenalex-snapshot
Highly efficient procedure for the conjugate addition of amines to electron deficient alkenes catalyzed by novel ionic liquid
inferred← citeshttps://doi.org/10.1007/s12039-013-0513-8openalex-snapshot
Two expedient ‘one-pot’ methods for synthesis of β-aryl-β-mercaptoketones over anhydrous potassium carbonate or amberlyst-15 catalyst
inferred← citeshttps://doi.org/10.1007/s12633-014-9245-8openalex-snapshot
Aza-Michael Addition of γ-Aminopropylsilatranes to Substituted N-Phenylmaleimides: Design and Synthesis of a Heterocyclic Amine Receptor and Their Preliminary Antimicrobial Studies
inferred← citeshttps://doi.org/10.1007/s42452-020-2281-7openalex-snapshot
Water hyacinth ash: an efficient green catalyst for the synthesis of β-amino carbonyl/nitrile compounds by aza-Michael reaction at room temperature
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00118-7openalex-snapshot
Antimony and Bismuth
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00401-8openalex-snapshot
4.01 Stabilized Nucleophiles with Electron Deficient Alkenes, Alkynes, Allenes
inferred← citeshttps://doi.org/10.1016/b978-0-443-18941-8.00012-2openalex-snapshot
Five-membered N-heterocycles–Part I
inferred← citeshttps://doi.org/10.1016/bs.apoc.2020.07.002openalex-snapshot
A brief insight into the physicochemical properties of room-temperature acidic ionic liquids and their catalytic applications in C C bond formation reactions
inferred← citeshttps://doi.org/10.1016/j.apcata.2011.08.015openalex-snapshot
Superbasic sodium stannate as catalyst for dehydrogenation, Michael addition and transesterification reactions
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.02.045openalex-snapshot
Metal–organic framework MOF-199 as an efficient heterogeneous catalyst for the aza-Michael reaction
inferred← citeshttps://doi.org/10.1016/j.apcata.2014.05.004openalex-snapshot
Bifunctional acid–base ionic liquid for the one-pot synthesis of fine chemicals: Thioethers, 2H-chromenes and 2H-quinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.01.020openalex-snapshot
Synthesis of dual-action parthenolide prodrugs as potent anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.10.010openalex-snapshot
Design, and facile synthesis of 1,3 diaryl-3-(arylamino)propan-1-one derivatives as the potential alpha-amylase inhibitors and antioxidants
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.03.044openalex-snapshot
Stereocontrolled synthesis of anticancer β-lactams via the Staudinger reaction
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.10.003openalex-snapshot
Indium(III) chloride catalyzed three-component coupling reaction: A novel synthesis of 2-substituted aryl(indolyl)kojic acid derivatives as potent antifungal and antibacterial agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.08.075openalex-snapshot
Iodine-catalyzed conjugate addition of indoles onto en-1,4-dione: A novel synthesis of 3-(1-(1H-indol-3-yl)-2-oxo-2-phenylethyl)indolin-2-ones as antibacterial and antifungal agents
inferred← citeshttps://doi.org/10.1016/j.catcom.2006.02.001openalex-snapshot
Bi(TFA)3 immobilized in [nbpy]FeCl4: An efficient catalyst system for the one-pot synthesis of 4,6-diarylpyrimidin-2(1H)-ones
inferred← citeshttps://doi.org/10.1016/j.catcom.2006.07.019openalex-snapshot
ZrCl4-catalyzed aza-Michael addition of carbamates to enones: Synthesis of Cbz-protected β-amino ketones
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.10.011openalex-snapshot
Ammonium chloride-catalyzed carbon–sulfur bond formation in water
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.11.002openalex-snapshot
Y(NO3)3· 6H2O catalyzed aza-Michael addition of aromatic/hetero-aromatic amines under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.catcom.2008.07.019openalex-snapshot
Bismuth(III) nitrate pentahydrate: a stoichiometric reagent for microwave induced mild and highly efficient aerial oxidation of aromatic aldehydes under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.cclet.2010.11.007openalex-snapshot
Tributylphosphine-catalyzed reaction of ethanethiol with alkynyl ketones
inferred← citeshttps://doi.org/10.1016/j.cclet.2011.05.015openalex-snapshot
A mild and highly efficient one-pot three-component reaction for carbon–sulfur bond formation catalyzed by potassium tert-butoxide
inferred← citeshttps://doi.org/10.1016/j.cclet.2011.06.006openalex-snapshot
Sulfamic acid as a cost-effective and recyclable solid acid catalyst for Friedel–Crafts alkylation of indole with α,β-unsaturated carbonyl compound and benzyl alcohol
inferred← citeshttps://doi.org/10.1016/j.cclet.2012.04.008openalex-snapshot
BF3·Et2O promoted conjugate addition of ethanethiol to electron-deficient alkynes
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.01.032openalex-snapshot
A simple, efficient and green procedure for Michael addition catalyzed by [C4dabco]OH ionic liquid
inferred← citeshttps://doi.org/10.1016/j.crci.2011.03.002openalex-snapshot
Ultrasound assisted synthesis of Cs2.5H0.5PW12O40: An efficient nano-catalyst for preparation of β-amino ketones via aza-Michael addition reactions
inferred← citeshttps://doi.org/10.1016/j.crci.2011.09.006openalex-snapshot
Lithium tetrafluoroborate catalyzed highly efficient inter- and intramolecular aza-Michael addition with aromatic amines
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.06.010openalex-snapshot
Bismuth nitrate-induced novel nitration of estradiol: An entry to new anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ica.2016.02.019openalex-snapshot
Synthesis and characterization of a magnetically separable novel FeO@L-DOPA@Cu nanocatalyst (L-DOPA = L-3,4-dihydroxyphenyylalanine): Asymmetric aza-Michael addition reaction
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.07.134openalex-snapshot
“Smart” chemistry and its application in peroxidase immobilization using different support materials
inferred← citeshttps://doi.org/10.1016/j.jksus.2022.102475openalex-snapshot
Catalytic multicomponent synthesis, biological evaluation, molecular docking and in silico ADMET studies of some novel 3-alkyl indoles
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.03.030openalex-snapshot
Ultrasound-irradiated Michael addition of amines to ferrocenylenones under solvent-free and catalyst-free conditions at room temperature
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.06.014openalex-snapshot
Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides
inferred← citeshttps://doi.org/10.1016/j.jscs.2024.101916openalex-snapshot
Silica supported Schiff-based palladium nanocatalyst for n-alkylation at room temperature
inferred← citeshttps://doi.org/10.1016/j.micromeso.2012.08.015openalex-snapshot
Ordered organo-inorganic hybrid mesoporous solid acid catalysts (Zr–TMS–TFA) for Michael addition of indoles with α,β-unsaturated carbonyl compounds under environmentally benign solvent free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.02.017openalex-snapshot
Metal nitrates catalysed O-glucosylation using acetyl glucal in organic solvents and ionic liquids: A comparative investigation
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.06.061openalex-snapshot
A recyclable protocol for aza-Michael addition of amines to α,β-unsaturated compounds using Cu-Al hydrotalcite
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.11.025openalex-snapshot
ZrOCl2·8H2O as a highly efficient and the moisture tolerant Lewis acid catalyst for Michael addition of amines and indoles to α, β-unsaturated ketones under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.01.004openalex-snapshot
Silica gel catalyzed highly selective CS bond formation via Michael addition of thiols to α,β-unsaturated ketones under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.04.028openalex-snapshot
Hetero-Michael addition of benzenethiol to cycloalkenones using cation-exchanged faujasites: Simultaneous acid–base bifunctional catalysis
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.08.021openalex-snapshot
A novel environmentally friendly process for carbon–sulfur bond formation catalyzed by montmorillonite clays
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.08.082openalex-snapshot
Amberlyst-15: An efficient reusable heterogeneous catalyst for aza-Michael reactions under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.09.005openalex-snapshot
Rapid N-tert-butoxycarbonylation of amines using Bi(NO3)3·5H2O as a mild and highly efficient catalyst under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.10.021openalex-snapshot
Polyaniline supported indium chloride: A reusable catalyst for organic transformations in water
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.01.007openalex-snapshot
Amberlyst-15: A mild, efficient and reusable heterogeneous catalyst for Michael addition of pyrroles to α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.01.014openalex-snapshot
Boric acid catalyzed thia-Michael reactions in water or alcohols
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.04.037openalex-snapshot
Organic synthesis in water: Green protocol for the conjugate addition of thiols to p-quinones
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.07.053openalex-snapshot
Green and mild protocol for hetero-Michael addition of sulfur and nitrogen nucleophiles in ionic liquid
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.10.004openalex-snapshot
Phosphomolybdic acid-supported silica gel as efficient and cost-effective solid acid for the benzylation of indoles with benzylic alcohols
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.11.015openalex-snapshot
Mg–Al hydrotalcites as efficient catalysts for aza-Michael addition reaction: A green protocol
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.11.023openalex-snapshot
Polystyrene-supported CuI–imidazole complex catalyst for aza-Michael reaction of imidazoles with α,β-unsaturated compounds
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.06.031openalex-snapshot
Room temperature solvent free aza-Michael reactions over nano-cage mesoporous materials
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.10.016openalex-snapshot
Synthesis, Elucidation, Hirshfeld surface analysis, and DFT calculations of 4-chloro-N-[2-(2-1H-indol-3-yl-acetylamino)-phenyl]-benzamide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127244openalex-snapshot
Design-based synthesis, molecular docking analysis of an anti-inflammatory drug, and geometrical optimization and interaction energy studies of an indole acetamide derivative
inferred← citeshttps://doi.org/10.1016/j.mtchem.2021.100667openalex-snapshot
Studying photocatalytic dye degradation with bismuth nitrate–derived catalysts using paper microzones method
inferred← citeshttps://doi.org/10.1016/j.rechem.2021.100158openalex-snapshot
Hypotheses for synthesis of novel chiral beta-amino-beta-lactams through amidines
inferred← citeshttps://doi.org/10.1016/j.tet.2004.03.052openalex-snapshot
Catalysis by ionic liquid: a simple, green and efficient procedure for the Michael addition of thiols and thiophosphate to conjugated alkenes in ionic liquid, [pmIm]Br
inferred← citeshttps://doi.org/10.1016/j.tet.2004.05.087openalex-snapshot
Zirconium triflate-catalyzed reactions of indole, 1-methylindole, and pyrrole with α,β-unsaturated ketone
inferred← citeshttps://doi.org/10.1016/j.tet.2005.01.017openalex-snapshot
A new approach for the synthesis of 2-substituted indole derivatives via Michael type adducts
inferred← citeshttps://doi.org/10.1016/j.tet.2005.07.095openalex-snapshot
Conjugate addition of indoles to α,β-unsaturated ketones using Cu(OTf)2 immobilized in ionic liquids
inferred← citeshttps://doi.org/10.1016/j.tet.2005.09.117openalex-snapshot
[HP(HNCH2CH2)3N]NO3: an efficient homogeneous and solid-supported promoter for aza and thia-Michael reactions and for Strecker reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.030openalex-snapshot
Convergent synthesis of PAMAM dendrimers using click chemistry of azide-functionalized PAMAM dendrons
inferred← citeshttps://doi.org/10.1016/j.tet.2006.09.026openalex-snapshot
1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans
inferred← citeshttps://doi.org/10.1016/j.tet.2006.09.041openalex-snapshot
Transition metal-catalyzed formation of CF3-substituted α,β-unsaturated alkene and the synthesis of α-trifluoromethyl substituted β-amino ester
inferred← citeshttps://doi.org/10.1016/j.tet.2006.09.052openalex-snapshot
The ionic liquid ethyltri-n-butylphosphonium tosylate as solvent for the acid-catalysed hetero-Michael reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2006.10.056openalex-snapshot
Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2006.10.077openalex-snapshot
Ionic liquid as catalyst and solvent: the remarkable effect of a basic ionic liquid, [bmIm]OH on Michael addition and alkylation of active methylene compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2006.11.037openalex-snapshot
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-promoted efficient and versatile aza-Michael addition
inferred← citeshttps://doi.org/10.1016/j.tet.2006.11.050openalex-snapshot
Scope and limitations of HClO4–SiO2 as an extremely efficient, inexpensive, and reusable catalyst for chemoselective carbon–sulfur bond formation
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.018openalex-snapshot
Ceric ammonium nitrate (CAN) as a green and highly efficient promoter for the 1,4-addition of thiols and benzeneselenol to α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.091openalex-snapshot
Catalytic conjugate addition of heterocyclic compounds to α,β-unsaturated carbonyl compounds by hafnium salts and scandium salts
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.088openalex-snapshot
Tributylphosphine, excellent organocatalyst for conjugate additions of non-nucleophilic N-containing compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.108openalex-snapshot
Michael additions of dihydropyrimidines and 2-amino-1,3,4-thiadiazoles to α,β-ethylenic compounds: using polyethylene glycols as a green reaction media
inferred← citeshttps://doi.org/10.1016/j.tet.2007.11.064openalex-snapshot
Fluoride ion-catalyzed conjugate addition for easy synthesis of 3-sulfanylpropionic acid from thiol and α,β-unsaturated carboxylic acid
inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.054openalex-snapshot
Features and applications of reactions of α,β-unsaturated N-acylbenzotriazoles with amino compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2009.01.071openalex-snapshot
A convenient synthesis of functionalized isoxazolines and related 5-hydroxyisoxazolidine-4-carboxylates
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.079openalex-snapshot
A facile generation of C–S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.05.010openalex-snapshot
Three components synthesis of homoallylic amines catalyzed by bismuth(III) nitrate pentahydrate
inferred← citeshttps://doi.org/10.1016/j.tet.2009.05.011openalex-snapshot
Stereocontrolled conjugate additions to dihydroindolizinone systems. Synthesis of enantiopure polysubstituted tetrahydropyrrolo[2,1-a]isoquinolones
inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.012openalex-snapshot
Catalytic carbon–sulfur bond formation by amphoteric vanadyl triflate: exploring with thia-Michael addition, thioacetalization, and transthioacetalization reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.001openalex-snapshot
Rongalite® and base-promoted cleavage of disulfides and subsequent Michael addition to α,β-unsaturated ketones/esters: an odorless synthesis of β-sulfido carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2010.05.054openalex-snapshot
An effective aza-Michael addition of aromatic amines to electron-deficient alkenes in alkaline Al2O3
inferred← citeshttps://doi.org/10.1016/j.tet.2010.08.017openalex-snapshot
Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of β-alkoxyketones by the oxa-Michael addition reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.082openalex-snapshot
Green, efficient and practical Michael addition of arylamines to α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.tet.2012.01.078openalex-snapshot
Stereospecific novel glycosylation of hydroxy ?-lactams via iodine-catalyzed reaction: a new method for optical resolution
inferred← citeshttps://doi.org/10.1016/j.tet.2012.04.070openalex-snapshot
Asymmetric synthesis of β-aryl-β-trifluoromethyl-β-aminoarones via Mannich-type reactions of ketone enolates with chiral aryl CF3-substituted N-tert-butanesulfinyl ketimines
inferred← citeshttps://doi.org/10.1016/j.tet.2012.06.009openalex-snapshot
Novel synthesis of 3-pyrrole substituted ?-lactams via microwave-induced bismuth nitrate-catalyzed reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2012.12.037openalex-snapshot
Chemo/regioselective Aza-Michael additions of amines to conjugate alkenes catalyzed by polystyrene-supported AlCl3
inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.070openalex-snapshot
Synthesis of new fluorescent building blocks via the microwave-assisted annulation reaction of 1,1,2-trimethyl-1H-benzo[e]indole with acrylic acid and its derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2019.02.041openalex-snapshot
Iodine-catalyzed coupling of β-hydroxyketones with aromatic amines to form β-aminoketones and Benzo[h]quinolones
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132482openalex-snapshot
Understanding water mediated proton migration in conversion of π-bond in olefinic carbon atoms into C–N bond to form β-amino adducts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.12.093openalex-snapshot
A mild, efficient and environmentally friendly method for the regio- and chemoselective synthesis of enaminones using Bi(TFA)3 as a reusable catalyst in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.04.053openalex-snapshot
Highly efficient phosphine-catalyzed aza-Michael reactions of α,β-unsaturated compounds with carbamates in the presence of TMSCl
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.08.060openalex-snapshot
Rhodium-catalyzed addition of alcohols to terminal enones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.11.156openalex-snapshot
One-pot synthesis of N-substituted (3-oxobutanyl)carbamates from primary amines using modified zeolite Hβ at room temperature
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.01.051openalex-snapshot
Copper(II) tetrafluoroborate as a novel and highly efficient catalyst for Michael addition of mercaptans to α,β-unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.02.103openalex-snapshot
A straightforward highly efficient Paal–Knorr synthesis of pyrroles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.02.153openalex-snapshot
Regioselective N- and C2-electrophilic substitution of 3-substituted indoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.03.112openalex-snapshot
Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.05.099openalex-snapshot
Iodine-catalyzed Michael addition of mercaptans to α,β-unsaturated ketones under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.05.108openalex-snapshot
Cu-nanoparticles: a chemoselective catalyst for the aza-Michael reactions of N-alkyl- and N-arylpiperazines with acrylonitrile
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.07.117openalex-snapshot
Bismuth(III) nitrate pentahydrate—a mild and inexpensive reagent for synthesis of coumarins under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.09.082openalex-snapshot
A simple and green procedure for the conjugate addition of thiols to conjugated alkenes employing polyethylene glycol (PEG) as an efficient recyclable medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.09.167openalex-snapshot
Boric acid: a novel and safe catalyst for aza-Michael reactions in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.10.037openalex-snapshot
Elongation of β-hydroxyenones by cross-metathesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.11.058openalex-snapshot
CAN and iodine-catalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.080openalex-snapshot
Iodine catalyzed conjugate addition of mercaptans to α,β-unsaturated carboxylic acids under solvent-free condition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.01.124openalex-snapshot
β-Cyclodextrin promoted aza-Michael addition of amines to conjugated alkenes in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.02.125openalex-snapshot
Synthesis of novel β-functionalized α-oximinoketones via hetero-Michael addition of alcohols and mercaptans to enones
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