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Relative reactivity and structures of benzoyltrimethylhydrazine and 1-benzoyl-2-methylpyrazolidine

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inferred← citeshttps://doi.org/10.2139/ssrn.4753791openalex-extracted
Theoretical Structure Determination of a Class of Heterocyclic Compounds: The Pyrazolidines
inferred← citeshttps://doi.org/10.1002/ange.201407801openalex-snapshot
Direct Spectroscopic Evidence of Hyperconjugation Unveils the Conformational Landscape of Hydrazides
inferred← citeshttps://doi.org/10.1002/ange.201609395openalex-snapshot
Peptide N‐Amination Supports β‐Sheet Conformations
inferred← citeshttps://doi.org/10.1002/anie.201407801openalex-snapshot
Direct Spectroscopic Evidence of Hyperconjugation Unveils the Conformational Landscape of Hydrazides
inferred← citeshttps://doi.org/10.1002/anie.201609395openalex-snapshot
Peptide N‐Amination Supports β‐Sheet Conformations
inferred← citeshttps://doi.org/10.1002/chin.198145204openalex-snapshot
ChemInform Abstract: RELATIVE REACTIVITY AND STRUCTURES OF BENZOYLTRIMETHYLHYDRAZINE AND 1‐BENZOYL‐2‐METHYLPYRAZOLIDINE
inferred← citeshttps://doi.org/10.1002/ejoc.200300416openalex-snapshot
N‐Acylhydrazines: Future Perspectives Offered by New Syntheses and Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.201300567openalex-snapshot
Conformational Behavior of 1:1 [α/α‐Hydrazino]mer, 1:1 [α/Aza‐β3‐amino]mer and 1:1 [Aza‐β3‐amino/α]mer Series: Three Series of Foldamers
inferred← citeshttps://doi.org/10.1002/hlca.200790237openalex-snapshot
Controlled Release of Volatile Aldehydes and Ketones from Dynamic Mixtures Generated by Reversible Hydrazone Formation
inferred← citeshttps://doi.org/10.1002/pep2.70008openalex-snapshot
Incorporation of Azapeptoid Residues Into Collagen
inferred← citeshttps://doi.org/10.1002/poc.807openalex-snapshot
Tetrahedral intermediates in reactions of carboxylic acid derivatives with nucleophiles
inferred← citeshttps://doi.org/10.1002/slct.72987openalex-snapshot
Effect of α‐Hydrazino Acids on the Performance of H‐Pro–Pro‐Xaa Catalysts in the Conjugate Addition of Aldehydes to Nitroolefins
inferred← citeshttps://doi.org/10.1007/bf01168555openalex-snapshot
Crystal and molecular structure of dimethylpyrazolo [1,2-a]pyrazolo[1,2-b]benzotriazole-3,4-dicarboxylate, C15H13N3O4
inferred← citeshttps://doi.org/10.1007/s11172-010-0018-2openalex-snapshot
Insertion of carbon disulfide and the nitrile group into the diaziridine ring of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes in ionic liquids catalyzed by BF3 · Et2O
inferred← citeshttps://doi.org/10.1007/s11172-010-0259-0openalex-snapshot
Reaction of 1-arylmethylidenepyrazolidin-1-azomethine imines with aryl ketenes
inferred← citeshttps://doi.org/10.1016/b978-008096519-2.00072-2openalex-snapshot
Pyrazoles and their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/b978-008096519-2.00133-8openalex-snapshot
Volume 5 References
inferred← citeshttps://doi.org/10.1016/bs.mie.2021.04.013openalex-snapshot
Synthesis and conformation of backbone N-aminated peptides
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.05.025openalex-snapshot
Tri-substituted acylhydrazines as tertiary amide bioisosteres: HCV NS5B polymerase inhibitors
inferred← citeshttps://doi.org/10.1016/j.cplett.2024.141293openalex-snapshot
Theoretical structure determination of a class of heterocyclic compounds: The pyrazolidines
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)00633-1openalex-snapshot
Fischer-type alkyl(hydrazino)carbene complexes: new synthetic potential in comparison with aminocarbene complexes
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91316-4openalex-snapshot
N-methoxy-n-methylamides as effective acylating agents
inferred← citeshttps://doi.org/10.1021/acs.accounts.4c00024openalex-snapshot
Beyond N-Alkylation: Synthesis, Structure, and Function of N-Amino Peptides
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03384openalex-snapshot
δ-Azaproline and Its Oxidized Variants
inferred← citeshttps://doi.org/10.1021/acsomega.4c00804openalex-snapshot
α-Hydrazino Acid Insertion Governs Peptide Organization in Solution by Local Structure Ordering
inferred← citeshttps://doi.org/10.1021/jacs.0c08427openalex-snapshot
Mechanism of an Organocatalytic Cope Rearrangement Involving Iminium Intermediates: Elucidating the Role of Catalyst Ring Size
inferred← citeshttps://doi.org/10.1021/jo201390bopenalex-snapshot
Z/E Isomerism in Nα-Nα-Disubstituted Hydrazides and the Amidoxy Bond: Application to the Conformational Analysis of Pseudopeptides Built of Hydrazinoacids and α-Aminoxyacids
inferred← citeshttps://doi.org/10.1039/d1cc04533dopenalex-snapshot
n N → π* Ar interactions stabilize the E -ac isomers of arylhydrazides and facilitate their S N Ar autocyclizations
inferred← citeshttps://doi.org/10.1080/00958979808027144openalex-snapshot
COPPER(II) COORDINATION COMPOUNDS: CLASSIFICATION AND ANALYSIS OF CRYSTALLOGRAPHIC AND STRUCTURAL DATA III. DIMERIC COMPOUNDS
inferred← citeshttps://doi.org/10.25135/acg.oc.16.17.00.012openalex-snapshot
Preparation and biological evaluation of novel acylhydrazide derivatives of 2,3-dichloronaphthoquinone
inferred← citeshttps://doi.org/10.3390/molecules27030787openalex-snapshot
Different Schiff Bases—Structure, Importance and Classification
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