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A Practical Synthesis of the Platelet Fibrinogen Antagonist, Elarofiban
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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2‐Skatylquinuclidine. A convenient synthesis of a 2‐aroylquinuclidine
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Synthetic oxytocics. I: 3‐(piperidyl‐(N)‐methyl‐)indoles and related compounds
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Principles of Peptide Synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)76775-xopenalex-snapshot
Approaches toward the total syntheses of astins A, B, and C
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An efficient stereoselective synthesis of methyl (S)-3-amino-3-(3-pyridyl)propanoate
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Piperidine Derivatives. XII. Local Anesthetics Derived from Reduction Products of Beta-Acetylpyridine
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Chemistry of emeriamine and its analogs and their inhibitory activity in long-chain fatty acid oxidation
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Potent, Orally Active GPIIb/IIIa Antagonists Containing a Nipecotic Acid Subunit. Structure−Activity Studies Leading to the Discovery of RWJ-53308
inferredcites →https://doi.org/10.1021/jo00050a007openalex-snapshot
Asymmetric synthesis of sulfinimines: applications to the synthesis of nonracemic .beta.-amino acids and .alpha.-hydroxyl .beta.-amino acids
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An alternate synthesis of deethylvincadifformine
inferredcites →https://doi.org/10.1021/op990192mopenalex-snapshot
An Expedient Method for Resolution of 3-Amino-3-(3‘-pyridyl)propionic Acid and Related Compounds
inferredcites →https://doi.org/10.1128/aac.32.8.1154openalex-snapshot
New class of antifungal agents: jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis species
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Design and Development of Efficient Synthetic Strategies for Novel B-Lactamase Enhancer: WCK 5153 Effective Against Gram-Negative Pathogens
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Design and Development of Efficient Synthetic Strategies for Novel B-Lactam Enhancer Wck 5153 Effective Against Gram-Negative Pathogens
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Chiral Lewis Base‐Catalyzed, Enantioselective Reduction of Unprotected β‐Enamino Esters with Trichlorosilane
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Chemoselektivität und die eigentümlichen Reaktivitäten funktioneller Gruppen
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Chemoselectivity and the Curious Reactivity Preferences of Functional Groups
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Practical Tactics in Resolution of Racemates via Diastereomeric Salt Formation
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Metal Analyses in Environmental and Pharmaceutical Samples by Capillary Electrophoresis with Methyl 3-Amino-3-(pyridin-3-yl)propanoate Dihydrochloride as a New Ion-Pairing Reagent
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Design and development of an efficient convergent synthetic strategy for novel β-lactam enhancer zidebactam (WCK 5107)
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Resolution of α/β-amino acids by enantioselective penicillin G acylase from Achromobacter sp.
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Design and development of efficient synthetic strategies for novel β-lactam enhancer WCK 5153 effective against gram-negative pathogens
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Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution
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Highly Efficient Synthesis of β-Amino Acid Derivatives via Asymmetric Hydrogenation of Unprotected Enamines
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Highly Efficient Iridium-Catalyzed Asymmetric Hydrogenation of Unprotected β-Enamine Esters
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Development of an Efficient Synthesis for a Nipecotate-Containing Immunopotentiator
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Practical, Catalytic Enantioselective Hydrogenation to Synthesize N-Unprotected β-Amino Esters
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Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals
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Protecting-group-free synthesis as an opportunity for invention
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Fe-catalysed Kumada-type alkyl–alkyl cross-coupling. Evidence for the intermediacy of Fe(i) complexes
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