On the public citation graph

Chemo- and Diastereoselective Reduction of .beta.-Enamino Esters: A Convenient Synthesis of Both cis- and trans-.gamma.-Amino Alcohols and .beta.-Amino Esters

https://doi.org/10.1021/jo00097a039
0 signed · 201 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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.4765444openalex-extracted
Cobalt(Ii) Catalyzed Michael-Type Hydroarylamination of Activated Olefins
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199902)1999:2<437::aid-ejoc437>3.0.co;2-vopenalex-snapshot
Synthesis of Enantiopure β- and γ-Amino Alcohols from Homochiral α- and β-Aminoacylsilanes as Stable Synthetic Equivalents of α- and β-Amino Aldehydes
inferred← citeshttps://doi.org/10.1002/(sici)1099-0801(199709)11:5<317::aid-bmc706>3.0.co;2-mopenalex-snapshot
Direct HPLC separation of ?-aminoester enantiomers on totally synthetic chiral stationary phases
inferred← citeshttps://doi.org/10.1002/9781118662083.cot05-010openalex-snapshot
Formation of Amines from Aldehydes, Ketones, and Derivatives
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.200505268openalex-snapshot
A General and Efficient Method for the Preparation of β‐Enamino Ketones and Esters Catalyzed by Indium Tribromide
inferred← citeshttps://doi.org/10.1002/adsc.200800368openalex-snapshot
p‐Toluenesulfonylmethyl Isocyanide (TosMIC) and Indium Manifold Strategy to Access β‐Keto‐(E)‐enamino Esters from 1,3‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.200900736openalex-snapshot
A Novel Strategy for the Construction of Functionalized 1,5‐ Benzodiazepines via a Tandem Conjugated Addition/Cyclization Process
inferred← citeshttps://doi.org/10.1002/ajoc.201900351openalex-snapshot
Oxidant‐Controlled Divergent Syntheses of Pyrazoles and Pyrroles by Copper(I)‐Catalyzed Oxidative Coupling of β‐Enamino Esters
inferred← citeshttps://doi.org/10.1002/ange.200705300openalex-snapshot
Organocatalytic Asymmetric Three‐Component Cyclization of Cinnamaldehydes and Primary Amines with 1,3‐Dicarbonyl Compounds: Straightforward Access to Enantiomerically Enriched Dihydropyridines
inferred← citeshttps://doi.org/10.1002/anie.200705300openalex-snapshot
Organocatalytic Asymmetric Three‐Component Cyclization of Cinnamaldehydes and Primary Amines with 1,3‐Dicarbonyl Compounds: Straightforward Access to Enantiomerically Enriched Dihydropyridines
inferred← citeshttps://doi.org/10.1002/aoc.5068openalex-snapshot
Some Novel Dinuclear phenylboronates of biologically potent β‐enaminoesters: Synthesis, Spectroscopic characterization, antimicrobial activity and their antiandrogenic effect
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/chem.201204594openalex-snapshot
A β‐Enaminone‐Initiated Multicomponent Domino Reaction for the Synthesis of Indoloquinolizines and Benzoquinolizines from Acyclic Precursors
inferred← citeshttps://doi.org/10.1002/chem.201402607openalex-snapshot
Fully Diastereoselective Synthesis of Polysubstituted, Functionalized Piperidines and Decahydroquinolines Based on Multicomponent Reactions Catalyzed by Cerium(IV) Ammonium Nitrate
inferred← citeshttps://doi.org/10.1002/chem.201601766openalex-snapshot
Resonance‐Assisted Hydrogen Bonding as a Driving Force in Synthesis and a Synthon in the Design of Materials
inferred← citeshttps://doi.org/10.1002/chem.201801046openalex-snapshot
Diastereoselective Synthesis of Highly Substituted, Amino‐ and Pyrrolidino‐Tetrahydrofurans as Lead‐Like Molecular Scaffolds
inferred← citeshttps://doi.org/10.1002/chin.199510087openalex-snapshot
ChemInform Abstract: Chemo‐ and Diastereoselective Reduction of β‐Enamino Esters: A Convenient Synthesis of Both cis‐ and trans‐γ‐Amino Alcohols and β‐Amino Esters.
inferred← citeshttps://doi.org/10.1002/chir.20812openalex-snapshot
Borane‐mediated asymmetric reduction of acetophenone by enantiopure aminonaphthols and aminoalcohols as catalytic source
inferred← citeshttps://doi.org/10.1002/cjoc.200990226openalex-snapshot
Sulfamic Acid as a Green and Reusable Catalyst for the Preparation of β‐Enaminones
inferred← citeshttps://doi.org/10.1002/dta.1712openalex-snapshot
Antimycobacterial evaluation of novel [4,5‐dihydro‐1H‐pyrazole‐1‐carbonyl]pyridine derivatives synthesized by microwave‐mediated Michael addition
inferred← citeshttps://doi.org/10.1002/ejoc.200500702openalex-snapshot
One‐Pot Addition/Reduction Procedure for the Synthesis of ‐Amino Alcohols from ‐Enamino Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.200600999openalex-snapshot
A Basic Ionic Liquid as Catalyst and Reaction Medium: A Rapid and Simple Procedure for Aza‐Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.200700667openalex-snapshot
Synthesis of New Trisubstituted 4‐Aminopiperidines as PAF‐Receptor Antagonists
inferred← citeshttps://doi.org/10.1002/ejoc.201500760openalex-snapshot
A Single Lipase‐Catalysed One‐Pot Protocol Combining Aminolysis Resolution and Aza‐Michael Addition: An Easy and Efficient Way to Synthesise β‐Amino Acid Esters
inferred← citeshttps://doi.org/10.1002/hc.20477openalex-snapshot
An efficient chemo‐ and stereoselective synthesis of enaminones and enaminoesters using (bromodimethyl)sulfonium bromide under solvent‐free conditions
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/jbt.23548openalex-snapshot
Syntheses and characterization of novel antimony (III) and bismuth (III) derivatives containing β‐enamino ester along with antimicrobial evaluation, DFT calculation, and cytotoxic study
inferred← citeshttps://doi.org/10.1002/jccs.200800032openalex-snapshot
Enamination of β‐Dicarbonyl Compounds with Amines
inferred← citeshttps://doi.org/10.1002/jhet.5570440635openalex-snapshot
Substituent effects in the ring‐chain tautomerism of 4‐alkyl‐2‐aryl substituted oxazolidines and tetrahydro‐1,3‐oxazines
inferred← citeshttps://doi.org/10.1002/jlac.1995199507163openalex-snapshot
On the preparation of β‐amino acids from α‐amino acids using the Arndt‐Eistert reaction: Scope, limitations and stereoselectivity. Application to carbohydrate peptidation. Stereoselective α‐alkylations of some β‐amino acids
inferred← citeshttps://doi.org/10.1002/slct.201802742openalex-snapshot
Nitroalkane‐Mediated Multicomponent Synthesis of β‐Enaminones
inferred← citeshttps://doi.org/10.1007/10551320_13openalex-snapshot
2 Hydrogen-1 NMR. References
inferred← citeshttps://doi.org/10.1007/10551320_14openalex-snapshot
2 Hydrogen-NMR. Coupling constant. References
inferred← citeshttps://doi.org/10.1007/10551320_2openalex-snapshot
2 Hydrogen-1 NMR. Introduction and Chemical shift. Substance no. 1ff
inferred← citeshttps://doi.org/10.1007/10551320_4openalex-snapshot
2 Hydrogen-1 NMR. Chemical shift. Substance no. 1844ff
inferred← citeshttps://doi.org/10.1007/10551320_6openalex-snapshot
2 Hydrogen-NMR. Coupling constant. Substance no. 1ff
inferred← citeshttps://doi.org/10.1007/10551320_7openalex-snapshot
2 Hydrogen-NMR. Coupling constant. Substance no. 1577ff
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_1443openalex-snapshot
Nuclear magnetic resonance data of C7H15NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_1474openalex-snapshot
Nuclear magnetic resonance data of C7H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_1776openalex-snapshot
Nuclear magnetic resonance data of C8H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2030openalex-snapshot
Nuclear magnetic resonance data of C9H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2195openalex-snapshot
Nuclear magnetic resonance data of C10H15NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2298openalex-snapshot
Nuclear magnetic resonance data of C10H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2337openalex-snapshot
Nuclear magnetic resonance data of C10H21NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2448openalex-snapshot
Nuclear magnetic resonance data of C11H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2449openalex-snapshot
Nuclear magnetic resonance data of C11H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2450openalex-snapshot
Nuclear magnetic resonance data of C11H17NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2506openalex-snapshot
Nuclear magnetic resonance data of C11H23NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2535openalex-snapshot
Nuclear magnetic resonance data of C12H13NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2564openalex-snapshot
Nuclear magnetic resonance data of C12H16BrNO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2581openalex-snapshot
Nuclear magnetic resonance data of C12H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2582openalex-snapshot
Nuclear magnetic resonance data of C12H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2583openalex-snapshot
Nuclear magnetic resonance data of C12H17NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2603openalex-snapshot
Nuclear magnetic resonance data of C12H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2604openalex-snapshot
Nuclear magnetic resonance data of C12H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2650openalex-snapshot
Nuclear magnetic resonance data of C12H23NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2731openalex-snapshot
Nuclear magnetic resonance data of C13H17NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2754openalex-snapshot
Nuclear magnetic resonance data of C13H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2755openalex-snapshot
Nuclear magnetic resonance data of C13H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2756openalex-snapshot
Nuclear magnetic resonance data of C13H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2757openalex-snapshot
Nuclear magnetic resonance data of C13H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2758openalex-snapshot
Nuclear magnetic resonance data of C13H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2759openalex-snapshot
Nuclear magnetic resonance data of C13H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2760openalex-snapshot
Nuclear magnetic resonance data of C13H19NO 2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2802openalex-snapshot
Nuclear magnetic resonance data of C13H25NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2856openalex-snapshot
Nuclear magnetic resonance data of C14H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2873openalex-snapshot
Nuclear magnetic resonance data of C14H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2874openalex-snapshot
Nuclear magnetic resonance data of C14H19NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2877openalex-snapshot
Nuclear magnetic resonance data of C14H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2878openalex-snapshot
Nuclear magnetic resonance data of C14H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2901openalex-snapshot
Nuclear magnetic resonance data of C14H21NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2903openalex-snapshot
Nuclear magnetic resonance data of C14H21NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_2962openalex-snapshot
Nuclear magnetic resonance data of C15H17NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3004openalex-snapshot
Nuclear magnetic resonance data of C15H21NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3005openalex-snapshot
Nuclear magnetic resonance data of C15H21NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3006openalex-snapshot
Nuclear magnetic resonance data of C15H21NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3007openalex-snapshot
Nuclear magnetic resonance data of C15H21NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3121openalex-snapshot
Nuclear magnetic resonance data of C16H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3137openalex-snapshot
Nuclear magnetic resonance data of C16H23NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_3193openalex-snapshot
Nuclear magnetic resonance data of C17H19NO2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_624openalex-snapshot
Nuclear magnetic resonance data of C4H11NO
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_881openalex-snapshot
Nuclear magnetic resonance data of C5H13NO
inferred← citeshttps://doi.org/10.1007/bf03245892openalex-snapshot
Cyanuric chloride catalysed rapid conversion of β-ketoesters into β-enaminoesters under mild and solvent-free conditions
inferred← citeshttps://doi.org/10.1007/bf03245934openalex-snapshot
Enantioselective conjugate addition to α,β-unsaturated esters and amides mediated by lithium perchlorate
inferred← citeshttps://doi.org/10.1007/s00726-011-1097-6openalex-snapshot
New 1,3-amino alcohols derived from enantiopure bridgehead β-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acids
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/s10563-013-9159-2openalex-snapshot
Copper Based Nanoparticles-Catalyzed Organic Transformations
inferred← citeshttps://doi.org/10.1007/s10600-025-04844-7openalex-snapshot
Three-Component Synthesis of Enaminones Based on Homoveratrylamine and Carbonyl Compounds
inferred← citeshttps://doi.org/10.1007/s11164-015-1950-4openalex-snapshot
[ADPQ][CH3COO]: efficient and recyclable catalyst for aza-Michael addition of α, β-unsaturated compounds and amines under solvent-free conditions
inferred← citeshttps://doi.org/10.1007/s11164-018-3454-5openalex-snapshot
β-Enaminones over recyclable nano-CoFe2O4: a highly efficient solvent-free green protocol
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/10.1016/0040-4020(95)00253-5openalex-snapshot
Some observations regarding the stereochemical course of iminium ion reductions: An example of the size difference between sodium cyanoborohydride and sodium triacetoxyborohydride
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00476-oopenalex-snapshot
A versatile route to β-enamino esters by acylation of lithium enamines with diethyl carbonate or benzyl chloroformate
inferred← citeshttps://doi.org/10.1016/0040-4020(95)01097-1openalex-snapshot
Simple synthesis of 2H-1,3-oxazines and their stereoselective transformation into 1,3-aminoalcohols and azetidines
inferred← citeshttps://doi.org/10.1016/0040-4020(95)01100-5openalex-snapshot
A new method for preparation of 3,6-dihydro-2H-1,3-oxazines and explorations of their use in stereoselective synthesis of 1,3-amino alcohol derivatives
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02258-9openalex-snapshot
Studies towards the synthesis of guanidine alkaloids; synthesis of a tricyclic guanidine from succinimide
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.11.048openalex-snapshot
5,6-Dihydro-1H-pyridin-2-ones as potent inhibitors of HCV NS5B polymerase
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.03.035openalex-snapshot
γ-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists
inferred← citeshttps://doi.org/10.1016/j.jics.2023.101119openalex-snapshot
Nanocatalyst driven synthesis of β-enaminones: A novel step towards the development of pharmaceutical precursors
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.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.2005.11.045openalex-snapshot
Highly efficient, mild and chemo- and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.04.065openalex-snapshot
Sc(OTf)3 catalyzed highly rapid and efficient synthesis of β-enamino compounds 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.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.molstruc.2013.04.029openalex-snapshot
Vibrational assignment and crystal structure of 3-amino-1-phenyl-2-buten-1-one
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.2006.03.109openalex-snapshot
Biocatalysis as a profound tool in the preparation of highly enantiopure β-amino acids
inferred← citeshttps://doi.org/10.1016/j.tet.2006.07.044openalex-snapshot
Regio- and stereoselective double alkylation of β-enamino esters with organolithium reagents followed by one-pot reduction: convenient method for the synthesis of tertiary γ-amino alcohols
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.2009.01.081openalex-snapshot
Studies on the Eschenmoser coupling reaction and insights on its mechanism. Application in the synthesis of Norallosedamine and other alkaloids
inferred← citeshttps://doi.org/10.1016/j.tet.2009.07.011openalex-snapshot
Ring opening of cyclic N,O-acetals with allyltrimethylsilane under Lewis acidic conditions
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.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.tetasy.2006.04.009openalex-snapshot
Stereoselective synthesis of enantiopure γ-aminoalcohols by reduction of chiral β-enaminoketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.04.016openalex-snapshot
Stereoselective synthesis of vicinal aminodiols, diamines and diaminols by the use of enantiopure aldehydes in the three-component aromatic Mannich-type reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.11.029openalex-snapshot
Efficient synthesis of (1R,2S) and (1S,2R)-2-aminocyclopentanecarboxylic acid ethyl ester derivatives in enantiomerically pure form
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.07.046openalex-snapshot
Efficient and practical asymmetric synthesis of 1-tert-butyl 3-methyl (3R,4R)-4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine-1,3-dicarboxylate, a useful intermediate for the synthesis of nociceptin antagonists
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.08.007openalex-snapshot
Novel stereoselective synthesis of 2,3-dihydro-1H-benzo[f]chromen-3-amine derivatives through a one-pot three-component reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.08.025openalex-snapshot
Stereoselective synthesis of new vicinal diaminoalkyl naphthols by three component Mannich type reaction of α,β-unsaturated aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.02.159openalex-snapshot
Direct synthesis of N-substituted, functionalized aspartic acids using alkali maleates and amines
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.2006.10.142openalex-snapshot
Significant rate acceleration of the aza-Michael reaction in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.059openalex-snapshot
Nanocrystalline copper(II) oxide catalyzed aza-Michael reaction and insertion of α-diazo compounds into N–H bonds of amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.051openalex-snapshot
Vanadium(IV) acetylacetonate catalyzed stereoselective synthesis of β-enaminoesters and β-enaminones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.11.037openalex-snapshot
Preparation and reactivity of [2-(3-methyl-4-nitro-isoxazol-5-yl)-vinyl]-amines
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2011.06.011openalex-snapshot
Ultrasound promoted the synthesis of N-propargylic β-enaminones
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)01056-5openalex-snapshot
A new and expeditious strategy for the synthesis of β-amino acids from Δ2-oxazolines
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00730-5openalex-snapshot
Synthesis of substituted piperidines, decahydroquinolines and octahydroindolizines by radical rearrangement reactions of 2-alkylideneaziridines
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00482-1openalex-snapshot
Synthesis of enantiomerically pure cis and trans 2-aminocyclopentanecarboxylic acids. Use of proline replacements in potential HIV-protease inhibitors
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10333-7openalex-snapshot
Stereoselective synthesis of 5-alkyliden-6-aminotetrahydro-2-pyranones through an unexpected isomerization of the hydroxytetrahydro-2-pyridinones obtained by the selective reduction of acylated enaminones
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01904-9openalex-snapshot
One-pot highly stereoselective reduction of β-keto amides to syn -γ-aminols
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00172-7openalex-snapshot
Stereoselective synthesis of β-aryl-β-amino esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01545-9openalex-snapshot
Stereoselective reduction of enaminones to syn γ-aminoalcohols
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00420-9openalex-snapshot
A concise and stereoselective synthesis of (+/−)-erythro-methylphenidate
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01894-2openalex-snapshot
A new route to α-hetero β-enamino esters using a mild and convenient solvent-free process assisted by focused microwave irradiation
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02469-1openalex-snapshot
A new and mild synthesis of β-amino acids from masked β-enamino acid derivatives
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60085-9openalex-snapshot
Synthesis, Stereochemistry and Transformations of Cyclopentane-, Cyclohexane-, Cycloheptane-, and Cyclooctane-Fused 1,3-Oxazines, 1,3-Thiazines, and Pyrimidines
inferred← citeshttps://doi.org/10.1016/s0957-4166(00)00198-1openalex-snapshot
Application of a new chiral stationary phase containing the glycopeptide antibiotic A-40,926 in the direct chromatographic resolution of β-amino acids
inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80028-9openalex-snapshot
The Chemistry of 2-Aminocyclopentanecarboxylic Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01393openalex-snapshot
Chiral Holmium Complex-Catalyzed Synthesis of Hydrocarbazole from Siloxyvinylindole and Its Application to the Enantioselective Total Synthesis of (−)-Minovincine
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00988openalex-snapshot
Gold-Catalyzed Hydroamination of Propargylic Alcohols: Controlling Divergent Catalytic Reaction Pathways To Access 1,3-Amino Alcohols, 3-Hydroxyketones, or 3-Aminoketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03846openalex-snapshot
Trisulfur-Radical-Anion-Triggered C(sp 2 )–H Amination of Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1021/cr000456zopenalex-snapshot
The Chemistry of 2-Aminocycloalkanecarboxylic Acids
inferred← citeshttps://doi.org/10.1021/ie070080gopenalex-snapshot
Aza-Michael Addition of Imidazoles to α,β-Unsaturated Compounds and Synthesis of β-Amino Alcohols via Nucleophilic Ring Opening of Epoxides Using Copper(II) Acetylacetonate (Cu(acac)2) Immobilized in Ionic Liquids
inferred← citeshttps://doi.org/10.1021/ja028090qopenalex-snapshot
Development of a New Lewis Acid-Catalyzed [3,3]-Sigmatropic Rearrangement: The Allenoate-Claisen Rearrangement
inferred← citeshttps://doi.org/10.1021/ja401034gopenalex-snapshot
Palladium-Catalyzed Intermolecular Dehydrogenative Aminohalogenation of Alkenes under Molecular Oxygen: An Approach to Brominated Enamines
inferred← citeshttps://doi.org/10.1021/jo000080popenalex-snapshot
A Convenient New Route to Piperidines, Pyrrolizidines, Indolizidines, and Quinolizidines by Cyclization of Acetylenic Sulfones with β- and γ-Chloroamines. Enantioselective Total Synthesis of Indolizidines(−)-167B,(−)-209D,(−)-209B, and(−)-207A
inferred← citeshttps://doi.org/10.1021/jo001662+openalex-snapshot
Preparation of Heterocycle-Masked β-Enamino Acids
inferred← citeshttps://doi.org/10.1021/jo010279hopenalex-snapshot
An Efficient Route to Either Enantiomer oftrans-2-Aminocyclopentanecarboxylic Acid
inferred← citeshttps://doi.org/10.1021/jo0108764openalex-snapshot
Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica Gel
inferred← citeshttps://doi.org/10.1021/jo026550sopenalex-snapshot
Bismuth Nitrate-Catalyzed Versatile Michael Reactions
inferred← citeshttps://doi.org/10.1021/jo051207jopenalex-snapshot
(S,S)-(+)-Pseudoephedrine as Chiral Auxiliary in Asymmetric Aza-Michael Reactions. Unexpected Selectivity Change when Manipulating the Structure of the Auxiliary
inferred← citeshttps://doi.org/10.1021/jo960107yopenalex-snapshot
Stereoselective Reduction of Enantiopure β-Enamino Esters by Hydride: A Convenient Synthesis of Both Enantiopure β-Amino Esters
inferred← citeshttps://doi.org/10.1021/jo961037yopenalex-snapshot
An Efficient and Simple Entry toN-Substituted β-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines
inferred← citeshttps://doi.org/10.1021/jo9809480openalex-snapshot
Synthesis and Reactivity of New β-Enamino Acid Derivatives: A Simple and General Approach to β-Enamino Esters and Thioesters
inferred← citeshttps://doi.org/10.1021/ol034827kopenalex-snapshot
Diastereoselective Synthesis of Fluorinated, Seven-Membered β-Amino Acid Derivatives via Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1021/ol1006086openalex-snapshot
Highly Enantioselective Relay Catalysis in the Three-Component Reaction for Direct Construction of Structurally Complex Heterocycles
inferred← citeshttps://doi.org/10.1021/ol302052copenalex-snapshot
A Unique Pathway for the 3-Aminobutyrate Starter Unit from l -Glutamate through β-Glutamate during Biosynthesis of the 24-Membered Macrolactam Antibiotic, Incednine
inferred← citeshttps://doi.org/10.1021/ol801738dopenalex-snapshot
Two-Step Stereocontrolled Synthesis of Densely Functionalized Cyclic β-Aminoesters Containing Four Stereocenters, Based on a New Cerium(IV) Ammonium Nitrate Catalyzed Sequential Three-Component Reaction
inferred← citeshttps://doi.org/10.1021/ol990774oopenalex-snapshot
First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters
inferred← citeshttps://doi.org/10.1021/op050202lopenalex-snapshot
Stereoselective Process for a CCR3 Antagonist
inferred← citeshttps://doi.org/10.1021/op060107sopenalex-snapshot
The Synthetic Versatility of Acyloxyborohydrides
inferred← citeshttps://doi.org/10.1039/9781849739634-00178openalex-snapshot
3.1.15. Michael Addition Reaction Followed by Elimination Under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1039/b803249aopenalex-snapshot
A revision for the synthesis of β-enaminones in solvent free conditions: efficacy of different supported heteropoly acids as active and reusable catalysts
inferred← citeshttps://doi.org/10.1039/c0ob00230eopenalex-snapshot
Diastereoselective syntheses of 3-aryl-5-(arylalkyl)-6-methyl-1-(1-phenylethyl)thioxotetrahydropyrimidin-4(1H)-ones: A stereochemical perspective from endo and exocyclic chiral centres
inferred← citeshttps://doi.org/10.1039/c0ob00965bopenalex-snapshot
An efficient biomaterial supported bifunctional organocatalyst (ES-SO3− C5H5NH+) for the synthesis of β-amino carbonyls
inferred← citeshttps://doi.org/10.1039/c2cc16997eopenalex-snapshot
Highly stereoselective synthesis of cis-β-enaminones mediated by diethyl azodicarboxylate
inferred← citeshttps://doi.org/10.1039/c2cc36129aopenalex-snapshot
Novel transformation of α,β-unsaturated aldehydes and ketones into γ-amino alcohols or 1,3-oxazines via a 4 or 5 step, one-pot sequence
inferred← citeshttps://doi.org/10.1039/c3cc46760kopenalex-snapshot
Expanding dynamic kinetic protocols: transaminase-catalyzed synthesis of α-substituted β-amino ester derivatives
inferred← citeshttps://doi.org/10.1039/c3ra23484copenalex-snapshot
Microwave assisted solvent and catalyst free method for novel classes of β-enaminoester and acridinedione synthesis
inferred← citeshttps://doi.org/10.1039/c5nj02437dopenalex-snapshot
Waste corn-cob cellulose supported bio-heterogeneous copper nanoparticles for aza-Michael reactions
inferred← citeshttps://doi.org/10.1039/c9gc01098jopenalex-snapshot
Electrochemical synthesis of enaminones via a decarboxylative coupling reaction
inferred← citeshttps://doi.org/10.1039/co9960300243openalex-snapshot
Carboxylic acids and esters
inferred← citeshttps://doi.org/10.1055/s-0036-1589080openalex-snapshot
Chiral Phosphinyl Enamines and Their Asymmetric Reduction through Group-Assisted Purification Chemistry Leading to Enantiopure β-Amino Esters/Amides
inferred← citeshttps://doi.org/10.1080/00397910701860968openalex-snapshot
K7[PW11CoO40]: Efficient and Ecofriendly Catalyst for the Enamination of β-Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1080/00397910902906594openalex-snapshot
Stereoselective Synthesis of β -Amino Ketones via Direct Mannich-Type Reaction Catalyzed with
inferred← citeshttps://doi.org/10.1080/00397911.2011.589020openalex-snapshot
Selective Reduction ofortho-Acylated β-Enaminones of Homoveratryamine and Their Cyclization to 1,2,3,4-Tetrahydroisoquinolines with β-Enaminone Moiety
inferred← citeshttps://doi.org/10.1080/00397911.2024.2414410openalex-snapshot
Cobalt(II) catalyzed Michael-type hydroamination of activated olefins
inferred← citeshttps://doi.org/10.1080/00397911003797775openalex-snapshot
Synthesis of Enaminones in Aqueous Media Using Catalytic Dilute HCl
inferred← citeshttps://doi.org/10.1080/10406638.2022.2118329openalex-snapshot
Microwave Assisted, H3PW12O40 Mediated Green Synthesis, Crystal Structure, in-Vitro Anti-Inflammatory and Anti-Oxidant Investigation of Enaminoketones
inferred← citeshttps://doi.org/10.1080/10426507.2010.492365openalex-snapshot
Silica Sulfuric Acid–Mediated Synthesis ofβ-Enaminones andβ-Enaminoesters Under Microwave Irradiation
inferred← citeshttps://doi.org/10.1081/scc-100105666openalex-snapshot
AN IMPROVED SYNTHESIS OF ENANTIOPURE β-AMINO ACIDS
inferred← citeshttps://doi.org/10.1107/s160053680800891xopenalex-snapshot
(Z)-Methyl 3-(4-ethoxyanilino)but-2-enoate
inferred← citeshttps://doi.org/10.1107/s1600536808016504openalex-snapshot
(Z)-3-[1-(4-Methoxyanilino)ethylidene]-4,5-dihydrofuran-2(3H)-one
inferred← citeshttps://doi.org/10.1134/s0023158411030207openalex-snapshot
Complex containing a Lewis acid and Brønsted acid for the catalytic reactions of aza-Michael addition
inferred← citeshttps://doi.org/10.1155/2013/473968openalex-snapshot
One‐Pot Solvent‐Free Three‐Component Synthesis of Conjugated Enaminones Containing Three Alkyl Carboxylate Groups
inferred← citeshttps://doi.org/10.1246/cl.2003.988openalex-snapshot
Aza-Michael Reactions in Ionic Liquids. A Facile Synthesis of β-Amino Compounds
inferred← citeshttps://doi.org/10.15826/chimtech/2017.4.2.029openalex-snapshot
Conjugated Addition of Amines to Electron Deficient Alkenes: A Green Approach
inferred← citeshttps://doi.org/10.2174/1570178618666210610155744openalex-snapshot
Oxa-Michael Addition Reactions of 3-hydroxy-2-azetidinones: Synthesis of 1, 3, 4-Trisubstituted-2-Azetidinones
inferred← citeshttps://doi.org/10.2174/2213335601666140610201546openalex-snapshot
aza-Michael Addition of Primary Amines by Lipases and Microwave Irradiation: A Green Protocol for the Synthesis of Propanenitrile Derivatives
inferred← citeshttps://doi.org/10.23850/22565035.721openalex-snapshot
Síntesis de ligantes Imino-Amida como modelos de ligantes orgánicos asociados a actividad factor tolerante a la glucosa
inferred← citeshttps://doi.org/10.26434/chemrxiv.12925238openalex-snapshot
O-Mesityl(sulfonyl)hydroxylamine: A Novel Reagent for Reduction of Electron Deficient α,β-Unsaturated Carbonyl Derivatives
inferred← citeshttps://doi.org/10.26434/chemrxiv.12925238.v1openalex-snapshot
O-Mesityl(sulfonyl)hydroxylamine: A Novel Reagent for Reduction of Electron Deficient α,β-Unsaturated Carbonyl Derivatives
inferred← citeshttps://doi.org/10.26434/chemrxiv.12925238.v2openalex-snapshot
O-Mesityl(sulfonyl)hydroxylamine: A Novel Reagent for Reduction of Electron Deficient α,β-Unsaturated Carbonyl Derivatives
inferred← citeshttps://doi.org/10.3184/030823405774663237openalex-snapshot
VCl 3 Catalysed Efficient Synthesis of β-enamine Esters and Ketones from β-keto Esters
inferred← citeshttps://doi.org/10.3390/molecules17010151openalex-snapshot
Synthesis of cis- and trans-3-Aminocyclohexanols by Reduction of β-Enaminoketones
inferred← citeshttps://doi.org/10.3762/bjoc.17.173openalex-snapshot
Recent advances in organocatalytic asymmetric aza-Michael reactions of amines and amides
showing the first 200 of 201 · page through all 201
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.