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Kinetics of Anionic Ring-Opening Polymerization of Variously Substituted β-Lactams: Homopolymerization and Copolymerization
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Molecular weight distribution of polyamides obtained in anionic polymerization of methyl-substituted ?-lactams and aminolysis of theirN-benzoyl lactams
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β‐Lactams, Their Polymerization and Use as Raw Materials for Fibers
inferredcites →https://doi.org/10.1002/bip.20391openalex-snapshot
Helices and other secondary structures of β‐ and γ‐peptides
inferredcites →https://doi.org/10.1002/masy.19860060104openalex-snapshot
Reactivity of lactams in anionic polymerization
inferredcites →https://doi.org/10.1002/masy.19900320110openalex-snapshot
Effect of reaction medium on ionic lactam polymerization
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Copolymerization. I. Kinetics and some experimental considerations of a general theory
inferredcites →https://doi.org/10.1002/pol.1950.120050210openalex-snapshot
Linear method for determining monomer reactivity ratios in copolymerization
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Analysis of the linear methods for determining copolymerization reactivity ratios. IV. A comprehensive and critical reexamination of carbocationic copolymerization data
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Free‐radical copolymerization of styrene with butyl acrylate. II. Elemental kinetic copolymerization step predictions from homopolymerization data
inferredcites →https://doi.org/10.1002/polc.5070740126openalex-snapshot
An unusual kinetics of anionic polymerization of four‐membered lactams
inferredcites →https://doi.org/10.1007/978-1-4615-4183-7openalex-snapshot
Copolymerization : toward a systematic approach
inferredcites →https://doi.org/10.1016/j.jmb.2008.03.047openalex-snapshot
Dual Mechanism of Bacterial Lethality for a Cationic Sequence-Random Copolymer that Mimics Host-Defense Antimicrobial Peptides
inferredcites →https://doi.org/10.1016/j.polymer.2005.11.003openalex-snapshot
Polymerization of lactams, 96☆ anionic copolymerization of ε-caprolactam with ω-laurolactam
inferredcites →https://doi.org/10.1016/j.polymer.2008.04.059openalex-snapshot
Kinetic study of atom transfer radical homo- and copolymerization of styrene and methyl methacrylate initiated with trichloromethyl-terminated poly(vinyl acetate) macroinitiator
inferredcites →https://doi.org/10.1016/s0032-3861(96)00566-6openalex-snapshot
Polyamides from lactams via anionic ring-opening polymerization: 1. Chemistry and some recent findings
inferredcites →https://doi.org/10.1016/s0079-6700(00)00018-6openalex-snapshot
Ring-opening polymerization of lactams. Living anionic polymerization and its applications
inferredcites →https://doi.org/10.1021/cr000045iopenalex-snapshot
β-Peptides: From Structure to Function
inferredcites →https://doi.org/10.1021/cr00054a001openalex-snapshot
Effect of conformational change on reactivity in organic chemistry. Evaluations, applications, and extensions of Curtin-Hammett Winstein-Holness kinetics
inferredcites →https://doi.org/10.1021/ja0110022openalex-snapshot
Controlled Polymerization of β-Lactams Using Metal−Amido Complexes: Synthesis of Block Copoly(β-peptides)
inferredcites →https://doi.org/10.1021/ja01237a052openalex-snapshot
Copolymerization. I. A Basis for Comparing the Behavior of Monomers in Copolymerization; The Copolymerization of Styrene and Methyl Methacrylate
inferredcites →https://doi.org/10.1021/ja077288dopenalex-snapshot
Mimicry of Antimicrobial Host-Defense Peptides by Random Copolymers
inferredcites →https://doi.org/10.1021/ja8069192openalex-snapshot
Access to Poly-β-Peptides with Functionalized Side Chains and End Groups via Controlled Ring-Opening Polymerization of β-Lactams
inferredcites →https://doi.org/10.1021/ja901613gopenalex-snapshot
Structure−activity Relationships among Random Nylon-3 Copolymers That Mimic Antibacterial Host-Defense Peptides
inferredcites →https://doi.org/10.1021/ja9050636openalex-snapshot
Nylon-3 Copolymers that Generate Cell-Adhesive Surfaces Identified by Library Screening
inferredcites →https://doi.org/10.1021/ma60050a009openalex-snapshot
Synthesis and Polymerization of Substituted β-Propiolactams
inferredcites →https://doi.org/10.1080/00222337508068644openalex-snapshot
Analysis of the Linear Methods for Determining Copolymerization Reactivity Ratios. I. A New Improved Linear Graphic Method
inferredcites →https://doi.org/10.1080/00222337608060768openalex-snapshot
Analysis of Linear Methods for Determining Copolymerization Reactivity Ratios. III. Linear Graphic Method for Evaluating Data Obtained at High Conversion Levels
inferredcites →https://doi.org/10.1098/rspa.1950.0022openalex-snapshot
Studies in copolymerization II. A discussion of the validity of the results and some theoretical implications
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The mechanism and kinetics of the heterogeneous polymerization of vinyl monomers III. The benzoyl peroxide catalyzed copolymerization of vinyl and vinylidene chlorides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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In Situ Generation of Magnesium‐ and Calcium‐Based Grignard Reagents for Amide Synthesis
inferred← citeshttps://doi.org/10.1002/pen.25171openalex-snapshot
Anionic copolymerization of nylon 6/12: A comprehensive review
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Cyclic Monomers: Epoxides, Lactide, Lactones, Lactams, Cyclic Silicon-Containing Monomers, Cyclic Carbonates, and Others
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00161-xopenalex-snapshot
Other Fused Azetidines, Azetines and Azetes
inferred← citeshttps://doi.org/10.1016/b978-0-444-53349-4.00109-6openalex-snapshot
Ring-Opening Polymerization of Cyclic Amides (Lactams)
inferred← citeshttps://doi.org/10.1016/j.jpba.2023.115773openalex-snapshot
A strategic approach towards mass balance investigations in pharmaceutical drug substance release testing: A peculiar out of specification case study encountered during API manufacture
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One-Shot Synthesis of Peptide Amphiphiles with Applications in Directed Graphenic Assembly
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00510openalex-snapshot
Guidelines for β-Lactam Synthesis: Glycal Protecting Groups Dictate Stereoelectronics and [2+2] Cycloaddition Kinetics
inferred← citeshttps://doi.org/10.1021/acsami.8b01117openalex-snapshot
Surface Modified with a Host Defense Peptide-Mimicking β-Peptide Polymer Kills Bacteria on Contact with High Efficacy
inferred← citeshttps://doi.org/10.1021/acsapm.6c03383openalex-snapshot
Ring-Strain-Driven One-Shot Synthesis of Glycosylated Cationic Block β-Peptides with Improved In Vivo Pharmacokinetics and Biodistribution
inferred← citeshttps://doi.org/10.1021/acsmacrolett.0c00227openalex-snapshot
Dewar Heterocycles as Versatile Monomers for Ring-Opening Metathesis Polymerization
inferred← citeshttps://doi.org/10.1021/bm2013058openalex-snapshot
C-Terminal Functionalization of Nylon-3 Polymers: Effects of C-Terminal Groups on Antibacterial and Hemolytic Activities
inferred← citeshttps://doi.org/10.1021/ja305900ropenalex-snapshot
Poly-amido-saccharides: Synthesis via Anionic Polymerization of a β-Lactam Sugar Monomer
inferred← citeshttps://doi.org/10.1021/ja500367uopenalex-snapshot
Tuning the Biological Activity Profile of Antibacterial Polymers via Subunit Substitution Pattern
inferred← citeshttps://doi.org/10.1021/ja507576aopenalex-snapshot
Ternary Nylon-3 Copolymers as Host-Defense Peptide Mimics: Beyond Hydrophobic and Cationic Subunits
inferred← citeshttps://doi.org/10.1021/mz400239ropenalex-snapshot
Effects of Cyclic vs Acyclic Hydrophobic Subunits on the Chemical Structure and Biological Properties of Nylon-3 Copolymers
inferred← citeshttps://doi.org/10.1021/mz400394ropenalex-snapshot
Synthetic Enantiopure Carbohydrate Polymers That Are Highly Soluble in Water and Noncytotoxic
inferred← citeshttps://doi.org/10.1039/c1py00334hopenalex-snapshot
Nylon 3 synthesized by ring opening polymerization with a metal-free catalyst
inferred← citeshttps://doi.org/10.1039/c2cc33854hopenalex-snapshot
β-Peptide coatings by surface-initiated polymerization
inferred← citeshttps://doi.org/10.1039/c3sc52777hopenalex-snapshot
Synthesis of bioinspired carbohydrate amphiphiles that promote and inhibit biofilms
inferred← citeshttps://doi.org/10.1039/d0sc03647aopenalex-snapshot
Pd-catalyzed stereoselective tandem ring-opening amination/cyclization of vinyl γ-lactones: access to caprolactam diversity
inferred← citeshttps://doi.org/10.1039/d1cs00930copenalex-snapshot
Beyond nylon 6: polyamides via ring opening polymerization of designer lactam monomers for biomedical applications
inferred← citeshttps://doi.org/10.3390/polym10040357openalex-snapshot
Polymers and Related Composites via Anionic Ring-Opening Polymerization of Lactams: Recent Developments and Future Trends
inferred← citeshttps://doi.org/10.70675/5b12d169z9bdez40a7zbec7za0e9d69bacc0openalex-snapshot
Polyethers and polyamide-3 synthesis by monomer activated anionic polymerization
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