On the public citation graph
Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids
0 signed · 623 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.197801761openalex-snapshot
Production and Utilization of Amino Acids
inferredcites →https://doi.org/10.1002/anie.199300013openalex-snapshot
Marine Metabolites and Metal Ion Chelation: The Facts and the Fantasies
inferredcites →https://doi.org/10.1002/anie.199400151openalex-snapshot
Chemistry and Biology of Taxol
inferredcites →https://doi.org/10.1002/anie.199504551openalex-snapshot
Enantioselective Synthesis of β‐Amino Acids: TMS‐SAMP as a Chiral Ammonia Equivalent for the Aza Analogous Michael Addition to α,β‐Unsaturated Esters
inferredcites →https://doi.org/10.1002/hlca.19910740414openalex-snapshot
Versatile Stereoselective Synthesis of Completely Protected Trifunctional α‐Methylated α‐Amino Acids Starting from Alanine
inferredcites →https://doi.org/10.1007/978-3-642-82805-8openalex-snapshot
Modern Synthetic Methods 1986
inferredcites →https://doi.org/10.1007/bf01933994openalex-snapshot
The use of benzylpenicillinacylase fromEscherichia coli in the resolution of some racemicβ-,γ-,δ- andɛ-amino-acids
inferredcites →https://doi.org/10.1016/0014-5793(87)81308-xopenalex-snapshot
The chemistry and biochemistry of the amino acids
inferredcites →https://doi.org/10.1016/0040-4020(93)80005-eopenalex-snapshot
Self-reproduction of chirality. Asymmetric synthesis of β-alkyl-β-amino acids from enantiomerically pure dihydropyrimidinones
inferredcites →https://doi.org/10.1016/0040-4039(93)85112-aopenalex-snapshot
Microginin, an angiotensin-converting enzyme inhibitor from the blue-green alga Microcystis aeruginosa
inferredcites →https://doi.org/10.1016/0040-4039(94)88477-3openalex-snapshot
Onchidin: a cytotoxic depsipeptide with C2 symmetry from a marine mollusc
inferredcites →https://doi.org/10.1016/s0040-4020(01)80840-1openalex-snapshot
Recent developments in the stereoselective synthesis of α-aminoacids
inferredcites →https://doi.org/10.1016/s0040-4020(01)85527-7openalex-snapshot
Recent stereoselective synthetic approaches to β-amino acids
inferredcites →https://doi.org/10.1016/s0040-4020(01)86036-1openalex-snapshot
Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(01)87007-1openalex-snapshot
Synthesis and stereochemical behaviour of 8-alkyl-3-(1-phenylethyl)-7-oxa-1,3-diazabicyclo-[3.2.1]-octane-4,6-diones directed towards the synthesis of α-substituted β-amino acids
inferredcites →https://doi.org/10.1016/s0040-4039(00)73317-xopenalex-snapshot
Michael-type addition of phthalimide salts to chiral α,β-unsaturated imides
inferredcites →https://doi.org/10.1016/s0040-4039(00)76775-xopenalex-snapshot
Approaches toward the total syntheses of astins A, B, and C
inferredcites →https://doi.org/10.1016/s0040-4039(00)79067-8openalex-snapshot
Highly diastereoselective alkylation of 6-methylperihydropyrimidin-4-ones directed towards the synthesis of α-substituted β-amino acids
inferredcites →https://doi.org/10.1016/s0040-4039(00)84645-6openalex-snapshot
Jasplakinolide, a cyclodepsipeptide from the marine sponge, SP.
inferredcites →https://doi.org/10.1016/s0040-4039(00)91716-7openalex-snapshot
The synthesis of potent marcocyclic renin inhibitors
inferredcites →https://doi.org/10.1016/s0040-4039(00)91777-5openalex-snapshot
Isolation and Structure of Asterin, a new halogenated cyclic penta-peptide from Aster tataricus
inferredcites →https://doi.org/10.1016/s0040-4039(01)93104-1openalex-snapshot
Selective N-dealkylation of tertiary amines with vinyl chloroformate: An improved synthesis of naloxone
inferredcites →https://doi.org/10.1016/s0957-4166(00)80074-9openalex-snapshot
Metal-assisted aldol condensation of chiral 6-methyl perihydropyrimidin-4-ones
inferredcites →https://doi.org/10.1016/s0957-4166(00)80251-7openalex-snapshot
The asymmetric Michael addition reactions using chiral imines
inferredcites →https://doi.org/10.1016/s0957-4166(00)80511-xopenalex-snapshot
Preparation and assignment of configuration of 1-benzoyl- (2S)-tert-butyl-3-methyl-perhydropyrimidin-4-one. Useful starting material for the enantioselective synthesis of α-substituted β-amino acids
inferredcites →https://doi.org/10.1016/s0957-4166(00)82354-xopenalex-snapshot
Asymmetric synthesis of R-β-amino butanoic acid and S-β-tyrosine: Homochiral lithium amide equivalents for Michael additions to α,β-unsaturated esters.
inferredcites →https://doi.org/10.1016/s0957-4166(00)86173-xopenalex-snapshot
Asymmetric synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid: The unknown amino acid component of microginin
inferredcites →https://doi.org/10.1016/s0957-4166(00)86275-8openalex-snapshot
Origins of the high stereoselectivity in the conjugate addition of lithium(α-methylbenzyl)benzylamide to t-butyl cinnamate
inferredcites →https://doi.org/10.1016/s0960-8524(99)00145-5openalex-snapshot
Biotransformations in organic synthesis
inferredcites →https://doi.org/10.1021/ar00029a007openalex-snapshot
A dozen years of retro-inverso peptidomimetics
inferredcites →https://doi.org/10.1021/cr00097a003openalex-snapshot
The ester enolate-imine condensation route to .beta.-lactams
inferredcites →https://doi.org/10.1021/ja00031a039openalex-snapshot
Enantiomerically pure dihydropyrimidinones as reagents and auxiliaries for asymmetric synthesis
inferredcites →https://doi.org/10.1021/ja00096a020openalex-snapshot
Microsclerodermins A and B. Antifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp.
inferredcites →https://doi.org/10.1021/ja00271a062openalex-snapshot
Jaspamide, a modified peptide from a Jaspis sponge, with insecticidal and antifungal activity
inferredcites →https://doi.org/10.1021/ja00285a051openalex-snapshot
Enantioselective synthesis of .beta.-amino esters through high pressure-induced addition of amines to .alpha.,.beta.-ethylenic esters
inferredcites →https://doi.org/10.1021/jm00391a030openalex-snapshot
Chemistry of emeriamine and its analogs and their inhibitory activity in long-chain fatty acid oxidation
inferredcites →https://doi.org/10.1021/jo00004a005openalex-snapshot
Self-reproduction of chirality. Asymmetric synthesis of .beta.-aryl-.beta.-amino acids from enantiomerically pure dihydropyrimidinones
inferredcites →https://doi.org/10.1021/jo00007a053openalex-snapshot
Asymmetric synthesis of .beta.-amino acids. 1. Highly diastereoselective addition of a racemic .beta.-alanine enolate derivative to electrophiles
inferredcites →https://doi.org/10.1021/jo00030a010openalex-snapshot
A new route to the synthesis of amino acids through the mercury cyclization of chiral amidals
inferredcites →https://doi.org/10.1021/jo00034a037openalex-snapshot
Enantioselective synthesis of .beta.-amino acids. 2. Preparation of the like stereoisomers of 2-methyl- and 2-benzyl-3-aminobutanoic acid
inferredcites →https://doi.org/10.1021/jo00046a046openalex-snapshot
Keramamide F, a new thiazole-containing peptide from the Okinawan marine sponge Theonella sp
inferredcites →https://doi.org/10.1021/jo00064a011openalex-snapshot
Synthesis of .alpha.-substituted .alpha.-amino acids via cationic intermediates
inferredcites →https://doi.org/10.1021/jo00073a017openalex-snapshot
Lewis acid-promoted 1,4-addition to chiral imide derivatives in the synthesis of .beta.-amino acids
inferredcites →https://doi.org/10.1021/jo00074a016openalex-snapshot
Asymmetric synthesis of .alpha.-alkyl-.alpha. amino acids from chromium-carbene-complex-derived .beta.-lactams
inferredcites →https://doi.org/10.1021/jo00082a025openalex-snapshot
Asymmetric synthesis of erythro and threo .alpha.-substituted .beta.-amino esters
inferredcites →https://doi.org/10.1021/jo00103a020openalex-snapshot
Highly Diastereoselective Alkylation of Perhydropyrimidin-4-ones Directed toward the Synthesis of .alpha.-Substituted .beta.-Amino Acids. 2.
inferredcites →https://doi.org/10.1021/jo00106a027openalex-snapshot
A Three Component Coupling Approach to a Chiral 1.beta.-Methylcarbapenem Key Intermediate
inferredcites →https://doi.org/10.1021/jo00176a004openalex-snapshot
Structure of majusculamide C, a cyclic depsipeptide from Lyngbya majuscula
inferredcites →https://doi.org/10.1021/jo00241a033openalex-snapshot
Scytonemin A, a novel calcium antagonist from a blue-green alga
inferredcites →https://doi.org/10.1021/jo00364a041openalex-snapshot
Asymmetric Michael reactions of 3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepine with methyl crotonate
inferredcites →https://doi.org/10.1038/373264a0openalex-snapshot
Penicillin acylase has a single-amino-acid catalytic centre
inferredcites →https://doi.org/10.1039/c39930001660openalex-snapshot
Asymmetric synthesis of the β-lactam framework via a three-component coupling reaction
inferredcites →https://doi.org/10.1039/cs9932200183openalex-snapshot
Biosynthetic incorporation of non-natural amino acids into proteins
inferredcites →https://doi.org/10.1039/p19930001375openalex-snapshot
Asymmetric synthesis of homochiral syn- and anti-3-phenylisoserine derivatives: a practical strategy for the synthesis of the taxol C-13 side chain
inferredcites →https://doi.org/10.1039/p19940001129openalex-snapshot
Asymmetric synthesis of anti-α-alkyl-β-amino acids
inferredcites →https://doi.org/10.1039/p19940001141openalex-snapshot
Asymmetric synthesis of syn-α-alkyl-β-amino acids
inferredcites →https://doi.org/10.1042/bj2680249openalex-snapshot
Emerging approaches in the molecular design of receptor-selective peptide ligands: conformational, topographical and dynamic considerations
inferredcites →https://doi.org/10.1055/s-1993-22447openalex-snapshot
An Enzymatic Entry to Enantiopure β-Amino Acids
inferredcites →https://doi.org/10.1055/s-1993-22587openalex-snapshot
Asymmetric Synthesis of Allophenylnorstatine
inferredcites →https://doi.org/10.1055/s-1994-22760openalex-snapshot
A Succinct Asymmetric Synthesis of (2S,3R)-2-Methyl-3-aminopentanoic Acid Hydrochloride
inferredcites →https://doi.org/10.1055/s-1994-25688openalex-snapshot
Diastereo- and Enantioselective Synthesis of α- Substituted β-Amino Acid Esters by Tandem Michael-addition / α-Alkylation with TMS-SAMP as Chiral Equivalent of Ammonia
inferredcites →https://doi.org/10.1212/wnl.37.6.1094-aopenalex-snapshot
Basic Mechanisms of the Epilepsies
inferredcites →https://doi.org/10.1246/cl.1973.1319openalex-snapshot
THE MOLECULAR STRUCTURE OF CYCLOCHLOROTINE, A TOXIC CHLORINE-CONTAINING CYCLIC PENTAPEPTIDE
inferredcites →https://doi.org/10.1248/cpb.40.2251openalex-snapshot
Kynostatin (KNI-227 and -272, highly potent anti-HIV agents: conformationally constrained tripeptide inhibitors of HIV protease containing allophenylnorstatine.
inferredcites →https://doi.org/10.15227/orgsyn.073.0201openalex-snapshot
ENANTIOMERICALLY PURE b-AMINO ACIDS FROM 2-tert-BUTYL-1-CARBOMETHOXY-2,3-DIHYDRO-4(1H)-PYRIMIDINONE: (R)-3-AMINO-3-(p-METHOXYPHENYL)PROPIONIC ACID
inferredcites →https://doi.org/10.3987/com-88-s33openalex-snapshot
Isolation and Structure of the Cell Growth Inhibitory Depsipeptides Dolastatins 11 and 12
inferredcites →https://doi.org/10.3987/com-91-5930openalex-snapshot
Use of Chiral Amidals in the Synthesis of 6-Methylperihydropyrimidin-4-ones, Protected Form of b-Amino Acids
inferredcites →https://doi.org/10.7164/antibiotics.29.97openalex-snapshot
Bestatin, an inhibitor of aminopeptidase B, produced by actinomycetes.
inferredcites →https://doi.org/10.7164/antibiotics.41.530openalex-snapshot
Synthesis of 1-N-(D-threo- and racemic erythro-3-amino-2-hydroxybutanoyl)-2',3'-dideoxykanamycin A.
inferredcites →https://doi.org/10.7326/0003-4819-72-6-969_2openalex-snapshot
Basic Mechanisms of the Epilepsies.
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(199901)1999:1<155::aid-ejoc155>3.0.co;2-aopenalex-snapshot
A New Diastereoselective Synthesis ofanti-α-Alkyl α-Hydroxy β-Amino Acids
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199909)1999:9<2433::aid-ejoc2433>3.0.co;2-xopenalex-snapshot
The Synthesis of Novel Cyclic β-Amino Acids as Intermediates for the Preparation of Bicyclic β-Lactams
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980420)110:8<1096::aid-ange1096>3.0.co;2-zopenalex-snapshot
Moderne Varianten der Mannich-Reaktion
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000403)112:7<1379::aid-ange1379>3.0.co;2-9openalex-snapshot
Enantioselectiveβ-Amino Acid Synthesis Based on Catalyzed Asymmetric Acyl Halide – Aldehyde Cyclocondensation Reactions
inferred← citeshttps://doi.org/10.1002/(sici)1521-3773(20000403)39:7<1323::aid-anie1323>3.0.co;2-xopenalex-snapshot
Enantioselective -Amino Acid Synthesis Based on Catalyzed Asymmetric Acyl Halide – Aldehyde Cyclocondensation Reactions
inferred← citeshttps://doi.org/10.1002/1099-0690(200007)2000:13<2489::aid-ejoc2489>3.0.co;2-7openalex-snapshot
Synthesis of the Phenylserine−Leucine Dipeptide Fragment Present in the Antibiotic Lysobactin from an Aziridine-2-imide Precursor
inferred← citeshttps://doi.org/10.1002/1439-7633(20010601)2:6<445::aid-cbic445>3.0.co;2-ropenalex-snapshot
The Outstanding Biological Stability ofβ- andγ-Peptides toward Proteolytic Enzymes: An In Vitro Investigation with Fifteen Peptidases
inferred← citeshttps://doi.org/10.1002/1521-3757(20011203)113:23<4507::aid-ange4507>3.0.co;2-2openalex-snapshot
Neues über die enantioselektive Synthese vonβ-Lactamen: Entwicklung der ersten katalytischen Ansätze
inferred← citeshttps://doi.org/10.1002/1615-9314(20020701)25:10/11<648::aid-jssc648>3.0.co;2-dopenalex-snapshot
Liquid chromatographic direct resolution of β-amino acids on a chiral crown ether stationary phase
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0345openalex-snapshot
Aspects of the Synthesis, Structure and Reactivity of Lithium Enolates
inferred← citeshttps://doi.org/10.1002/9781118517413.ch2openalex-snapshot
Introduction to Unnatural Foldamers
inferred← citeshttps://doi.org/10.1002/9781119640929.ch4openalex-snapshot
Chemoenzymatic Synthesis of Pharmacologically Active Compounds Containing Chiral 1,2‐Amino Alcohol Moiety
inferred← citeshttps://doi.org/10.1002/9783527619382.ch24openalex-snapshot
Enantioselective Hydrogenation: Phospholane Ligands
inferred← citeshttps://doi.org/10.1002/9783527623839.ch15openalex-snapshot
Nitrilase‐ and Nitrile Hydratase‐Catalyzed Enantioselective Preparation of Non‐Proteinogenic Amino Acids
inferred← citeshttps://doi.org/10.1002/9783527631766.ch7openalex-snapshot
Recent Developments in the Synthesis of β‐Amino Acids
inferred← citeshttps://doi.org/10.1002/9783527631827.ch6openalex-snapshot
Medicinal Chemistry of α‐Hydroxy‐β‐Amino Acids
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.200600593openalex-snapshot
Efficient Heterogeneously Palladium‐Catalysed Heck Arylation of Acrolein Diethyl Acetal. Selective Synthesis of Cinnamaldehydes or 3‐Arylpropionic Esters
inferred← citeshttps://doi.org/10.1002/adsc.200800328openalex-snapshot
Glycerol as An Efficient Promoting Medium for Organic Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200900084openalex-snapshot
Copper(I)‐Catalyzed Asymmetric Addition of Terminal Alkynes to β‐Imino Esters: An Efficient and Direct Method in the Synthesis of Chiral β3‐Alkynyl β2,2‐Dimethyl Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.200900189openalex-snapshot
The Use of Samarium Enolates, A Novel Alternative in the Addition Reactions to Imines. Synthesis of 3‐Amino Esters, Amides and Enantiopure 3,4‐Diamino Esters
inferred← citeshttps://doi.org/10.1002/adsc.200900534openalex-snapshot
The Addition Reaction of Samarium Enolates and 2‐Haloenolates Derived from Esters, and Amides to Imines. Totally Stereoselective Synthesis of Enantiopure 3,4‐Diamino Esters or Amides
inferred← citeshttps://doi.org/10.1002/adsc.201300135openalex-snapshot
Organocatalytic Asymmetric Mannich Reactions of 5H‐Oxazol‐4‐ones: Highly Enantio‐ and Diastereoselective Synthesis of Chiral α‐Alkylisoserine Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201500519openalex-snapshot
Metal‐Free Synthesis of Chlorinated β‐Amino Ketones via an Unexpected Reaction of Imines with Arylacetylenes in 1,1,1,3,3,3‐Hexafluoro‐2‐propanol
inferred← citeshttps://doi.org/10.1002/adsc.201501061openalex-snapshot
Chiral Lewis Base‐Catalyzed, Enantioselective Reduction of Unprotected β‐Enamino Esters with Trichlorosilane
inferred← citeshttps://doi.org/10.1002/adsc.201600026openalex-snapshot
An Enantioselective Three‐Component Sulfa‐Michael/Aldol Cascade Reaction and its Application to the Synthesis of Thioaryl Substituted (−)‐Bestatin Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.202300666openalex-snapshot
Advances in Catalytic Asymmetric Construction of Quaternary Stereogenic Centers by Conjugate Addition to β,β‐Disubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/advs.202403470openalex-snapshot
Enantioselective Aminosilylation of Alkenes by Palladium/Ming‐Phos‐Catalyzed Tandem Narasaka–Heck/Silylation Reaction
inferred← citeshttps://doi.org/10.1002/ange.19971092324openalex-snapshot
Ein effizientes Verfahren zur asymmetrischen Aminohydroxylierung
inferred← citeshttps://doi.org/10.1002/ange.200390211openalex-snapshot
Herstellung und asymmetrische Hydrierung β‐arylsubstituierter β‐Acylaminoacrylate
inferred← citeshttps://doi.org/10.1002/ange.200603188openalex-snapshot
Prolin‐katalysierte Mannich‐Reaktion von Aldehyden mit N‐Boc‐Iminen
inferred← citeshttps://doi.org/10.1002/ange.200604389openalex-snapshot
Efficient Trapping of Oxonium Ylides with Imines: A Highly Diastereoselective Three‐Component Reaction for the Synthesis of β‐Amino‐α‐hydroxyesters with Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.200705310openalex-snapshot
Catalytic Synthesis of β3‐Amino Acid Derivatives from α‐Amino Acids
inferred← citeshttps://doi.org/10.1002/ange.201209142openalex-snapshot
Copper‐Catalyzed Intermolecular Aminocyanation and Diamination of Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201310983openalex-snapshot
Intramolecular Aminocyanation of Alkenes by NCN Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.201901591openalex-snapshot
The Generation of Difluoroketenimine and Its Application in the Synthesis of α,α‐Difluoro‐β‐amino Amides
inferred← citeshttps://doi.org/10.1002/ange.202014686openalex-snapshot
Triazenyl Alkynes as Versatile Building Blocks in Multicomponent Reactions: Diastereoselective Synthesis of β‐Amino Amides
inferred← citeshttps://doi.org/10.1002/ange.202305042openalex-snapshot
Nickel‐Catalyzed Kinetic Resolution of Racemic Unactivated Alkenes via Enantio‐, Diastereo‐, and Regioselective Hydroamination
inferred← citeshttps://doi.org/10.1002/ange.202514155openalex-snapshot
Asymmetric Radical Coupling to Form β2,2,3‐Amino Acid Esters by Synergistic Chiral Phosphoric Acid and Photocatalysis
inferred← citeshttps://doi.org/10.1002/anie.199726371openalex-snapshot
A Highly Efficient Aminohydroxylation Process
inferred← citeshttps://doi.org/10.1002/anie.200390242openalex-snapshot
Preparation and Asymmetric Hydrogenation of β‐Aryl‐Substituted β‐Acylaminoacrylates
inferred← citeshttps://doi.org/10.1002/anie.200603188openalex-snapshot
Proline‐Catalyzed Mannich Reaction of Aldehydes with N‐Boc‐Imines
inferred← citeshttps://doi.org/10.1002/anie.200604389openalex-snapshot
Efficient Trapping of Oxonium Ylides with Imines: A Highly Diastereoselective Three‐Component Reaction for the Synthesis of β‐Amino‐α‐hydroxyesters with Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.200705310openalex-snapshot
Catalytic Synthesis of β3‐Amino Acid Derivatives from α‐Amino Acids
inferred← citeshttps://doi.org/10.1002/anie.201209142openalex-snapshot
Copper‐Catalyzed Intermolecular Aminocyanation and Diamination of Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201310983openalex-snapshot
Intramolecular Aminocyanation of Alkenes by NCN Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.201901591openalex-snapshot
The Generation of Difluoroketenimine and Its Application in the Synthesis of α,α‐Difluoro‐β‐amino Amides
inferred← citeshttps://doi.org/10.1002/anie.202014686openalex-snapshot
Triazenyl Alkynes as Versatile Building Blocks in Multicomponent Reactions: Diastereoselective Synthesis of β‐Amino Amides
inferred← citeshttps://doi.org/10.1002/anie.202305042openalex-snapshot
Nickel‐Catalyzed Kinetic Resolution of Racemic Unactivated Alkenes via Enantio‐, Diastereo‐, and Regioselective Hydroamination
inferred← citeshttps://doi.org/10.1002/anie.202514155openalex-snapshot
Asymmetric Radical Coupling to Form β 2,2,3 ‐Amino Acid Esters by Synergistic Chiral Phosphoric Acid and Photocatalysis
inferred← citeshttps://doi.org/10.1002/aoc.3457openalex-snapshot
Lanthanum immobilized on chitosan: a highly efficient heterogeneous catalyst for facile synthesis of novel (α,β‐unsaturated) β‐aminoketones
inferred← citeshttps://doi.org/10.1002/asia.201200575openalex-snapshot
Total Synthesis of (−)‐Kopsinine by an Asymmetric One‐Pot [N+2+3] Cyclization
inferred← citeshttps://doi.org/10.1002/asia.201300102openalex-snapshot
Chiral Calcium Iodide for Asymmetric Mannich‐type Reactions of Malonates with Imines Providing β‐Aminocarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/bip.20088openalex-snapshot
β2‐amino acids—syntheses, occurrence in natural products, and components of β‐peptides1,2
inferred← citeshttps://doi.org/10.1002/bkcs.11019openalex-snapshot
A Catalyst‐free Addition Reaction of Zinc Amide Enolates to N‐Sulfonyl Imines
inferred← citeshttps://doi.org/10.1002/bmc.237openalex-snapshot
Liquid chromatographic separation of the enantiomers of β‐amino acids on a ligand exchange chiral stationary phase
inferred← citeshttps://doi.org/10.1002/cbdv.200490087openalex-snapshot
The World of β‐ and γ‐Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components
inferred← citeshttps://doi.org/10.1002/cbdv.202502861openalex-snapshot
Design, Synthesis, and Anti‐Inflammatory Activity of Functionalized 1,2,4,5‐Tetrasubstituted‐Pyrimidinone
inferred← citeshttps://doi.org/10.1002/cbic.200300827openalex-snapshot
Probing the Proteolytic Stability of β‐Peptides Containing α‐Fluoro‐ and α‐Hydroxy‐β‐Amino Acids
inferred← citeshttps://doi.org/10.1002/cctc.201200135openalex-snapshot
Advances and Applications in Organocatalytic Asymmetric aza‐Michael Addition
inferred← citeshttps://doi.org/10.1002/cctc.201601208openalex-snapshot
Asymmetric Catalytic Syntheses of Pharmaceutically Important β ‐Amino‐ α ‐Hydroxyl Esters by Enantioselective Aminolysis of Methyl Phenylglycidate
inferred← citeshttps://doi.org/10.1002/cctc.201900575openalex-snapshot
Enantioselective Copper(II)/Box‐Catalyzed Synthesis of Chiral β3‐Tryptophan Derivatives
inferred← citeshttps://doi.org/10.1002/cctc.202100503openalex-snapshot
Improving Catalytic Activity and Reversing Enantio‐Specificity of ω‐Transaminase by Semi‐Rational Engineering en Route to Chiral Bulky β‐Amino Esters
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.200700594openalex-snapshot
Asymmetric Hydrogenation of α‐Primary and Secondary Amino Ketones: Efficient Asymmetric Syntheses of (−)‐Arbutamine and (−)‐Denopamine
inferred← citeshttps://doi.org/10.1002/chem.200900884openalex-snapshot
Chemoselective Synthesis of Substituted Imines, Secondary Amines, and β‐Amino Carbonyl Compounds from Nitroaromatics through Cascade Reactions on Gold Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201003265openalex-snapshot
Synthesis of 1,2‐Amino Alcohols by Sigmatropic Rearrangements of 3‐(N‐Tosylamino)allylic Alcohol Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201304509openalex-snapshot
Gold/Acid‐Co‐catalyzed Direct Microwave‐Assisted Synthesis of Fused Azaheterocycles from Propargylic Hydroperoxides
inferred← citeshttps://doi.org/10.1002/chem.201402519openalex-snapshot
Synthesis and Analysis of the Conformational Preferences of 5‐Aminomethyloxazolidine‐2,4‐dione Scaffolds: First Examples of β 2 ‐ and β 2, 2 ‐Homo‐Freidinger Lactam Analogues
inferred← citeshttps://doi.org/10.1002/chem.201604606openalex-snapshot
Catalytic Enantioselective Aza‐Reformatsky Reaction with Cyclic Imines
inferred← citeshttps://doi.org/10.1002/chem.201700464openalex-snapshot
β2, 2‐Amino Acid N‐Carboxyanhydrides Relying on Sequential Enantioselective C(4)‐Functionalization of Pyrrolidin‐2,3‐diones and Regioselective Baeyer–Villiger Oxidation
inferred← citeshttps://doi.org/10.1002/chem.201902009openalex-snapshot
Asymmetric Synthesis of β2‐Aryl Amino Acids through Pd‐Catalyzed Enantiospecific and Regioselective Ring‐Opening Suzuki–Miyaura Arylation of Aziridine‐2‐carboxylates
inferred← citeshttps://doi.org/10.1002/chin.199648292openalex-snapshot
ChemInform Abstract: Asymmetric Synthesis of β‐Amino Acids and α‐Substituted . beta.‐Amino Acids
inferred← citeshttps://doi.org/10.1002/chin.200302254openalex-snapshot
The Asymmetric Synthesis of Unnatural α‐Amino Acids as Building Blocks for Complex Molecule Synthesis
inferred← citeshttps://doi.org/10.1002/chir.20442openalex-snapshot
Liquid chromatographic direct resolution of β‐amino acids on a doubly tethered chiral stationary phase containing NH amide linkage based on (+)‐(18‐crown‐6)‐ 2,3,11,12‐tetracarboxylic acid
inferred← citeshttps://doi.org/10.1002/chir.20909openalex-snapshot
Asymmetric reduction of β‐ketoesters and chiral β‐iminoesters: Impact of a α‐quaternary stereocenter
inferred← citeshttps://doi.org/10.1002/chir.21986openalex-snapshot
Chiral cinchona alkaloid‐derived thiourea catalyst for enantioselective synthesis of novel β‐amino esters by mannich reaction
inferred← citeshttps://doi.org/10.1002/chir.22484openalex-snapshot
Development of HPLC Chiral Stationary Phases Based on (+)‐(18‐Crown‐6)‐2,3,11,12‐tetracarboxylic Acid and Their Applications
inferred← citeshttps://doi.org/10.1002/chir.23304openalex-snapshot
A review on Arthrobacter sp. lipase: A versatile biocatalyst for the kinetic resolution to access enantiomerically pure/enriched compounds
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.200990064openalex-snapshot
Aza‐Michael Addition of Isatin and Phthalimide to Symmetrical Fumaric Esters in Ionic Liquid Media
inferred← citeshttps://doi.org/10.1002/cssc.202001561openalex-snapshot
Highly Efficient Synthesis of Amino Acids by Amination of Bio‐Derived Hydroxy Acids with Ammonia over Ru Supported on N‐Doped Carbon Nanotubes
inferred← citeshttps://doi.org/10.1002/cssc.202201241openalex-snapshot
Visible Light‐Induced Unactivated δ‐C(sp3)−H Amination of Alcohols Catalyzed by Iron
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.200390210openalex-snapshot
Asymmetric Synthesis of Protected β‐Substituted and β,β‐Disubstituted β‐Amino Acids Bearing Branched Hydroxyalkyl Side Chains and of Protected 1,3‐Amino Alcohols with Three Contiguous Stereogenic Centers from Allylic Sulfoximines and Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.200400392openalex-snapshot
A Convenient New Synthesis of 3‐Substituted β‐Lactams Formally Derived from 1‐(Aminomethyl)cyclopropanecarboxylic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.200500297openalex-snapshot
Synthesis of 3‐ and 4‐Hydroxy‐2‐aminocyclohexanecarboxylic Acids by Iodocyclization
inferred← citeshttps://doi.org/10.1002/ejoc.200500386openalex-snapshot
Synthesis of Glycidol‐ and Sugar‐Derived Bicyclic β‐ and γ/δ‐Amino Acids for Peptidomimetic Design
inferred← citeshttps://doi.org/10.1002/ejoc.200500838openalex-snapshot
A New Three‐Component Cascade Reaction to Yield 3‐Spirocyclopropanatedβ‐Lactams
inferred← citeshttps://doi.org/10.1002/ejoc.200600691openalex-snapshot
Borax as an Efficient Metal‐Free Catalyst for Hetero‐Michael Reactions in an Aqueous Medium
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.200900870openalex-snapshot
Dehydro‐β‐amino Acid Containing Peptides as Promising Sequences for Drug Development
inferred← citeshttps://doi.org/10.1002/ejoc.201000852openalex-snapshot
Functionalization of (2S)‐Isopropyl‐5‐iodo‐2,3‐dihydro‐4(H)‐pyrimidin‐4‐ones by a Suzuki–Miyaura Cross‐Coupling Reaction Using Aryltrifluoroborate Salts: Convenient Enantioselective Preparation of α‐Substituted β‐Amino Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201000984openalex-snapshot
Direct Access to Cumbersome Aminated Quaternary Centers by Hyperbaric Aza‐Michael Additions
inferred← citeshttps://doi.org/10.1002/ejoc.201001693openalex-snapshot
Ring‐Opening of Epoxides in Water
inferred← citeshttps://doi.org/10.1002/ejoc.201100493openalex-snapshot
Foldamers Based on Oxazolidin‐2‐ones
inferred← citeshttps://doi.org/10.1002/ejoc.201101624openalex-snapshot
Promiscuous Behavior of Rhizomucor miehei Lipase in the Synthesis of N‐Substituted β‐Amino Esters
inferred← citeshttps://doi.org/10.1002/ejoc.201201055openalex-snapshot
Carica papaya Lipase Catalysed Resolution of β‐Amino Esters for the Highly Enantioselective Synthesis of (S)‐Dapoxetine
inferred← citeshttps://doi.org/10.1002/ejoc.201300971openalex-snapshot
Construction of Enantioenriched Cyclic Compounds by Asymmetric Allylic Alkylation and Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/ejoc.201301775openalex-snapshot
Highly Diastereoselective Reaction of α‐Diazoesters with Aryl Alcohols and Isatin Imines: Rapid Access to Oxindole‐Derived α‐Alkoxy‐β‐amino Acid Derivatives with Two Adjacent Quaternary Carbon Centers
inferred← citeshttps://doi.org/10.1002/ejoc.201301823openalex-snapshot
Organocatalytic Mannich Reactions on a Carbapenem Core – Synthesis of Mannich Bases and Bicyclic Diazanonanes
inferred← citeshttps://doi.org/10.1002/ejoc.201301834openalex-snapshot
trans‐Hexahydrobenzoxazolidinones in the Enantioselective Synthesis of β2‐Amino Acids Containing Proteinogenic Side Chains
inferred← citeshttps://doi.org/10.1002/ejoc.201402221openalex-snapshot
Exploring the Reactivity of Chiral Glycidic Amides for Their Applications in Synthesis of Bioactive Compounds
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/ejoc.201600448openalex-snapshot
Controlling Cyclopeptide Backbone Conformation with β/α‐Hybrid Peptide–Heterocycle Scaffolds
inferred← citeshttps://doi.org/10.1002/ejoc.201701279openalex-snapshot
Catalytic Asymmetric Reactions Involving the Seven‐Membered Cyclic Imine Moieties Present in Dibenzo[b,f][1,4]oxazepines
inferred← citeshttps://doi.org/10.1002/ejoc.201801139openalex-snapshot
Diastereoselective Radical Couplings Enable the Asymmetric Synthesis of anti‐β‐Amino‐α‐hydroxy Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202000823openalex-snapshot
Consecutive Three‐Component Coupling‐Addition Synthesis of β‐Amino Enoates and 3‐Hydroxypyrazoles via Ethyl 3‐Arylpropiolates
inferred← citeshttps://doi.org/10.1002/ejoc.202300463openalex-snapshot
Construction of β ‐Phenylalanine Derivatives through Pd‐Catalyzed, C(sp 2 )−H ( ortho ) Functionalization
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.200290004openalex-snapshot
Enantioselective Synthesis of β‐Amino Acids, Part 13
inferred← citeshttps://doi.org/10.1002/hlca.200490073openalex-snapshot
Diastereoselective Electrophilic Amination of Chiral 1‐Benzoyl‐2,3,5,6‐tetrahydro‐3‐methyl‐2‐(1‐methylethyl)pyrimidin‐4(1H)‐one for the Asymmetric Syntheses of α‐Substituted α,β‐Diaminopropanoic Acids
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.200490234openalex-snapshot
Improved Protocol for the Three‐Component Biginelli Reactions and Biginelli‐Like Mannich Reactions of Carbamates, Aldehydes, and Ketones
inferred← citeshttps://doi.org/10.1002/hlca.200490280openalex-snapshot
Preparation of Protected β2‐ and β3‐Homocysteine, β2‐ and β3‐Homohistidine, and β2‐Homoserine for Solid‐Phase Syntheses
inferred← citeshttps://doi.org/10.1002/hlca.201200449openalex-snapshot
Microwave‐Assisted Synthesis of β‐Lactams and Cyclo‐β‐dipeptides
inferred← citeshttps://doi.org/10.1002/ijch.201700011openalex-snapshot
Fundamental Developments of Chiral Phase Chromatography in Connection with Enantioselective Synthesis of β‐Amino Acids
inferred← citeshttps://doi.org/10.1002/jccs.200000014openalex-snapshot
Theoretical Study Of β2,3‐Peptide Models
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/jctb.6203openalex-snapshot
Lipase‐catalyzed aza‐Michael addition of amines to acrylates in supercritical carbon dioxide
inferred← citeshttps://doi.org/10.1002/jhet.2963openalex-snapshot
Regioselective Mono‐aza‐Michael Additions of Divinyl Ketones with Benzotriazole and Other N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/jhet.5570450454openalex-snapshot
Convenient preparations of 2‐alkyl‐5‐oxopyrrolidine‐3‐carboxylic acids
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.70058openalex-snapshot
Recent Advances in the Chemistry of Morita–Baylis–Hillman ( MBH ) Carbonates: A Review
inferred← citeshttps://doi.org/10.1002/jhet.976openalex-snapshot
Antiselective Three‐Component Mannich Reactions in Thiopyran‐4‐one System
inferred← citeshttps://doi.org/10.1002/poc.493openalex-snapshot
Thermal and hyperbaric addition of N,N‐ and N,O‐ binucleophiles on cycloalkylidenic bromo esters
inferred← citeshttps://doi.org/10.1002/pola.22710openalex-snapshot
Synthesis of chiral micelles and nanoparticles from amino acid based monomers using RAFT polymerization
inferred← citeshttps://doi.org/10.1002/psc.1052openalex-snapshot
A divergent approach to the preparation of cysteine and serine analogs
inferred← citeshttps://doi.org/10.1002/psc.1272openalex-snapshot
VCD studies on cyclic peptides assembled from L ‐α‐amino acids and a trans‐2‐aminocyclopentane‐ or trans‐2‐aminocyclohexane carboxylic acid
inferred← citeshttps://doi.org/10.1002/slct.201601486openalex-snapshot
An Auxiliary‐Mediated Alkylation Approach Towards the Synthesis of β‐Amino Carbonyl Derivatives
inferred← citeshttps://doi.org/10.1002/slct.74579openalex-snapshot
A Practicable Aza‐Michael Addition of Aniline and Acrylonitrile Using Dual Functions of Deep Eutectic Solvent (DES): Facile Synthesis of β ‐Aminonitrile Compounds
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_2009_11openalex-snapshot
β-Lactam Ring Opening: A Useful Entry to Amino Acids and Relevant Nitrogen-Containing Compounds
inferred← citeshttps://doi.org/10.1007/978-94-007-1712-1_7openalex-snapshot
Water as Reaction Medium in the Synthetic Processes Involving Epoxides
inferred← citeshttps://doi.org/10.1007/bf01388175openalex-snapshot
From?-lactams to?- and?-amino acid derived peptides
inferred← citeshttps://doi.org/10.1007/bf02446523openalex-snapshot
The use of β-amino acids in the design of protease and peptidase inhibitors
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/bf03246110openalex-snapshot
Some applications of zirconium(IV) tetrachloride (ZrCl4) and zirconium(IV) oxydichloride octahydrate (ZrOCl2.8H2O) as catalysts or reagents in organic synthesis
inferred← citeshttps://doi.org/10.1007/bf03247223openalex-snapshot
Hydrated ferric perchlorate, Fe(ClO4)3.XH2O in organic synthesis. A short review
inferred← citeshttps://doi.org/10.1007/s00216-008-2564-0openalex-snapshot
Enantioseparation of nonproteinogenic amino acids
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/s00706-011-0570-yopenalex-snapshot
Ecofriendly and efficient procedure for hetero-Michael addition reactions with an acidic ionic liquid as catalyst and reaction medium
inferred← citeshttps://doi.org/10.1007/s00726-015-2152-5openalex-snapshot
Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters
inferred← citeshttps://doi.org/10.1007/s00726-017-2439-9openalex-snapshot
Highly functionalized cyclic β-amino acid moieties as promising scaffolds in peptide research and drug design
inferred← citeshttps://doi.org/10.1007/s10311-013-0400-zopenalex-snapshot
Fast and efficient synthesis of N-substituted β-aminobutyric acids by grinding at room temperature
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/s10563-013-9159-2openalex-snapshot
Copper Based Nanoparticles-Catalyzed Organic Transformations
inferred← citeshttps://doi.org/10.1007/s10593-011-0774-4openalex-snapshot
Biologically active cyclic polypeptides with fragments of β-amino acid derivatives isolated from marine organisms (review)
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/s11164-015-2260-6openalex-snapshot
A review on green Lewis acids: zirconium(IV) oxydichloride octahydrate (ZrOCl2·8H2O) and zirconium(IV) tetrachloride (ZrCl4) in organic chemistry
inferred← citeshttps://doi.org/10.1007/s11224-012-0017-zopenalex-snapshot
Solvent-free synthesis and crystal structures of s-cis and s-trans N,N′-bis(2-hydroxycyclohexyl)ethane-1,2-diamine
inferred← citeshttps://doi.org/10.1007/s11224-021-01735-9openalex-snapshot
Michael addition of ethyl anthranilate and phenyl monothioanthranilate to acetylenic esters: experimental and theoretical results
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/b978-0-08-097774-4.00611-2openalex-snapshot
Enantioselective Hydrogenation of CC and CX Bonds
inferred← citeshttps://doi.org/10.1016/j.aca.2008.03.052openalex-snapshot
Liquid chromatographic resolution of β-amino acids on CSPs based on optically active (3,3′-diphenyl-1,1′-binaphthyl)-20-crown-6
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.12.039openalex-snapshot
Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity
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.2007.11.002openalex-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.ccr.2007.09.013openalex-snapshot
Synthesis of β-aminoacid derivatives via enantioselective hydrogenation of β-substituted-β-(acylamino)acrylates
inferred← citeshttps://doi.org/10.1016/j.checat.2023.100873openalex-snapshot
Arylamine synthesis enabled by a photocatalytic skeletal-editing dehydrogenative aromatization strategy
inferred← citeshttps://doi.org/10.1016/j.chroma.2003.08.070openalex-snapshot
Direct and indirect high-performance liquid chromatographic enantioseparation of β-amino acids
inferred← citeshttps://doi.org/10.1016/j.chroma.2007.09.054openalex-snapshot
High-performance liquid chromatographic enantioseparation of β-3-homo-amino acid stereoisomers on a (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid-based chiral stationary phase
inferred← citeshttps://doi.org/10.1016/j.chroma.2016.07.049openalex-snapshot
Liquid chromatographic enantioseparations on crown ether-based chiral stationary phases
inferred← citeshttps://doi.org/10.1016/j.crci.2010.03.005openalex-snapshot
A practical and efficient green synthesis of β-aminophosphoryl compounds via the aza-Michael reaction in water
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.inoche.2010.02.009openalex-snapshot
Crystallographic and computational investigation of nitrate salts of nickel(II) ethylenediamine complexes
inferred← citeshttps://doi.org/10.1016/j.jmgm.2017.02.008openalex-snapshot
Toward an ab initio potential energy surface for paclitaxel: A C-13 isoserine side chain conformational study
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.2014.06.028openalex-snapshot
Cobalt-catalyzed hydrogenation of β-enamino esters using an internal mixture of bidentate and monodentate ligands
inferred← citeshttps://doi.org/10.1016/j.jpba.2020.113149openalex-snapshot
Impurity profiling of l-aspartic acid and glycine using high-performance liquid chromatography coupled with charged aerosol and ultraviolet detection
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.2006.08.082openalex-snapshot
Amberlyst-15: An efficient reusable heterogeneous catalyst for aza-Michael reactions under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.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.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.molcatb.2003.10.010openalex-snapshot
Biotransformation of β-amino nitriles: the role of the N-protecting group
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129858openalex-snapshot
Synthesis, crystallographic characterization and Hirshfeld surface analysis of metal complexes of conformationally constrained β-amino acid, 2-(1-aminocyclohexyl)acetic acid with CoII, NiII, CuII and ZnII ions
inferred← citeshttps://doi.org/10.1016/j.procbio.2012.07.026openalex-snapshot
New biocatalytic route for the production of enantioenriched β-alanine derivatives starting from 5- and 6-monosubstituted dihydrouracils
inferred← citeshttps://doi.org/10.1016/j.rechem.2020.100036openalex-snapshot
NH4Cl Catalyzed synthesis of β-amino Esters
inferred← citeshttps://doi.org/10.1016/j.tet.2003.11.012openalex-snapshot
LiClO4 Accelerated Michael addition of amines to α,β-unsaturated olefins under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2004.02.052openalex-snapshot
An electrochemical interpretation of the mechanism of the chemical decarboxylation of 6-carboxyperhydropyrimidin-4-ones
inferred← citeshttps://doi.org/10.1016/j.tet.2004.03.084openalex-snapshot
Truncated diastereoselective Passerini reaction, a rapid construction of polysubstituted oxazole and peptides having an α-hydroxy-β-amino acid component
inferred← citeshttps://doi.org/10.1016/j.tet.2005.02.057openalex-snapshot
Synthesis and microbial transformation of β-amino nitriles
inferred← citeshttps://doi.org/10.1016/j.tet.2005.04.054openalex-snapshot
Concise and diastereoselective approach to syn- and anti-N-tosyl-α-hydroxy β-amino acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2005.06.094openalex-snapshot
Preparation of both enantiomers of β2-(3,4-dihydroxybenzyl)-β-alanine, higher homologues of Dopa
inferred← citeshttps://doi.org/10.1016/j.tet.2006.03.070openalex-snapshot
Tandem aza-Michael additions under high pressure: a shortcut to the azanorbornyl skeleton
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.2006.06.040openalex-snapshot
Chiral ligand-controlled asymmetric conjugate amination of enoates with lithium mesitylmethyl(trimethylsilyl)amide
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.2007.11.021openalex-snapshot
Efficient synthesis of 3-hydroxymethylated cis- and trans-cyclobutane β-amino acids using an intramolecular photocycloaddition strategy
inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.024openalex-snapshot
Synthesis of β2-homophenylalanine derivatives by Negishi cross-coupling reactions
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.2008.06.053openalex-snapshot
New approach to exclusive formation of both enantiomers of β-amino acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2009.05.037openalex-snapshot
Catalytic enantioselective conjugate addition of aromatic amines to fumarate derivatives: asymmetric synthesis of aspartic acid derivatives
showing the first 200 of 552 · page through all 552
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.