Matches in SemOpenAlex for { <https://semopenalex.org/work/W410950918> ?p ?o ?g. }
Showing items 1 to 63 of
63
with 100 items per page.
- W410950918 abstract "1. Introduction.- 1.1. Ring-Chain Isomeric Interconversions. General Considerations.- 1.2. Tautomerism or Isomerism? System Mobility and Equilibrium Position.- 1.3. Methods of Investigation of Ring-Chain Addition Tautomerism.- 1.3.1. Chemical Methods.- 1.3.2. Visible and UV Spectroscopy.- 1.3.3. IR Spectroscopy.- 1.3.4. Nuclear Magnetic Resonance.- 1.3.5. Mass Spectrometry.- 1.3.6. X-Ray Diffraction Analysis.- 1.3.7. Polarography.- 1.3.8. Other Physical Methods.- References.- 2. Intramolecular Reversible Addition Reactions to the C=O Group.- 2.1. Aldehydo and Keto-carboxylic Acids and Their Derivatives Modified at the Carboxylic Group.- 2.1.1. Aldehydo- and Keto-carboxylic Acids.- 2.1.2. Acyl Chlorides.- 2.1.3. Amides, Hydrazides, and Amidines.- 2.1.4. Esters.- 2.1.5. Mixed Anhydrides.- 2.2. Hydroxy Aldehydes and Ketones and Related Compounds.- 2.2.1. Derivatives Containing a Hydroxy Group at Carbon (C-OH).- 2.2.2. Derivatives Containing a Hydroxy Group at Nitrogen (N-OH).- 2.3. Amino Aldehydes and Ketones and Related Compounds.- 2.3.1. Covalent Hydration of Nitrogen-Containing Heterocycles.- 2.3.2. Derivatives Containing Amino Groups at sp3-, Aromatic, and sp2-Carbon Atoms.- 2.3.3. Urea and Thiourea Derivatives.- 2.3.4. Dithiocarbamates.- 2.3.5. Sulfonamides and Sulfinamides.- 2.3.6. Pyridones.- 2.3.7. 1,3-Diazaheterocycles.- 2.3.8. Triazenes.- 2.3.9. Miscellaneous.- 2.4. Intramolecular Migration of O-, N-, and S-Acyl Groups.- 2.5. Oxa-, Aza-, and Thiacyclols.- 2.6. Mercapto Aldehydes and Ketones and Related Compounds.- 2.7. Intramolecular Addition of C-H Groups.- References.- 3. Intramolecular Reversible Addition Reactions to the C=N Group.- 3.1. OH-Derivatives of Imines, Hydrazones, Oximes, and Nitrones.- 3.1.1. N-(Hydroxyalkyl) and N-(hydroxyaryl) imines.- 3.1.2. N-Hydroxyalkylhydrazones.- 3.1.3. Hydroxyalkyl and Hydroxyiminoalkyl Nitrones.- 3.1.4. Imines, Hydrazones, and Oximes of Hydroxyaldehydes and Hydroxyketones.- 3.1.5. Imines of Ketocarboxylic Acids.- 3.1.6. Fused Systems.- 3.2. N-H-Derivatives of Imines, Hydrazones, Oximes, and Nitrones.- 3.2.1. N-Aminoalkylimines.- 3.2.2. N-Aminoalkyl and N-Aminoacyl Hydrazones and Related Compounds.- 3.2.3. 2-Benzimidoyl-benzamides and -benzenesulfonamides.- 3.2.4. N-(2- and 3-Hydroxyiminoalkyl)nitrones.- 3.2.5. Fused Systems.- 3.3. S-H-Derivatives of Imines and Hydrazones.- 3.4. Miscellaneous.- References.- 4. Intramolecular Reversible Addition Reactions to Other Groups.- 4.1. Addition to the C?N Group.- 4.2. Addition to C=C and C?C Groups.- 4.3. Addition to the P=O Group.- 4.4. Addition to the P=N Group.- 4.5. Addition to the S=O Group.- 4.6. Addition to the Se=O Group.- 4.7. Addition to the I=O Group.- References.- 5. Generalizations Concerning the Influence of Structural and External Factors on the Relative Stability of Ring and Chain Isomers.- 5.1. Structural Influences.- 5.1.1. Electronic Effects of Substituents at Interacting Groups.- 5.1.2. Steric Effects of Substituents at Interacting Groups.- 5.1.3. Structure of the Connecting Link.- 5.1.4. Steric Effects of the Substituents at the Connecting Link.- 5.1.5. Intramolecular Hydrogen Bonds.- 5.2. Influence of External Factors.- References." @default.
- W410950918 created "2016-06-24" @default.
- W410950918 creator A5008465073 @default.
- W410950918 creator A5019880202 @default.
- W410950918 creator A5082158198 @default.
- W410950918 date "1985-01-01" @default.
- W410950918 modified "2023-09-24" @default.
- W410950918 title "Ring-chain tautomerism" @default.
- W410950918 hasPublicationYear "1985" @default.
- W410950918 type Work @default.
- W410950918 sameAs 410950918 @default.
- W410950918 citedByCount "12" @default.
- W410950918 countsByYear W4109509182013 @default.
- W410950918 countsByYear W4109509182017 @default.
- W410950918 crossrefType "book" @default.
- W410950918 hasAuthorship W410950918A5008465073 @default.
- W410950918 hasAuthorship W410950918A5019880202 @default.
- W410950918 hasAuthorship W410950918A5082158198 @default.
- W410950918 hasConcept C111233374 @default.
- W410950918 hasConcept C155647269 @default.
- W410950918 hasConcept C178790620 @default.
- W410950918 hasConcept C185592680 @default.
- W410950918 hasConcept C2779074116 @default.
- W410950918 hasConcept C2780378348 @default.
- W410950918 hasConcept C2780538656 @default.
- W410950918 hasConcept C71240020 @default.
- W410950918 hasConcept C75079739 @default.
- W410950918 hasConceptScore W410950918C111233374 @default.
- W410950918 hasConceptScore W410950918C155647269 @default.
- W410950918 hasConceptScore W410950918C178790620 @default.
- W410950918 hasConceptScore W410950918C185592680 @default.
- W410950918 hasConceptScore W410950918C2779074116 @default.
- W410950918 hasConceptScore W410950918C2780378348 @default.
- W410950918 hasConceptScore W410950918C2780538656 @default.
- W410950918 hasConceptScore W410950918C71240020 @default.
- W410950918 hasConceptScore W410950918C75079739 @default.
- W410950918 hasLocation W4109509181 @default.
- W410950918 hasOpenAccess W410950918 @default.
- W410950918 hasPrimaryLocation W4109509181 @default.
- W410950918 hasRelatedWork W1516740401 @default.
- W410950918 hasRelatedWork W2012160801 @default.
- W410950918 hasRelatedWork W2019418638 @default.
- W410950918 hasRelatedWork W2021026407 @default.
- W410950918 hasRelatedWork W2023271753 @default.
- W410950918 hasRelatedWork W2024189207 @default.
- W410950918 hasRelatedWork W2081165312 @default.
- W410950918 hasRelatedWork W2143981217 @default.
- W410950918 hasRelatedWork W2774031884 @default.
- W410950918 hasRelatedWork W2949202158 @default.
- W410950918 hasRelatedWork W2949351979 @default.
- W410950918 hasRelatedWork W2950223278 @default.
- W410950918 hasRelatedWork W2950439631 @default.
- W410950918 hasRelatedWork W2950770885 @default.
- W410950918 hasRelatedWork W2950851664 @default.
- W410950918 hasRelatedWork W2952037671 @default.
- W410950918 hasRelatedWork W2952794741 @default.
- W410950918 hasRelatedWork W2953068705 @default.
- W410950918 hasRelatedWork W2953072161 @default.
- W410950918 hasRelatedWork W2170049101 @default.
- W410950918 isParatext "false" @default.
- W410950918 isRetracted "false" @default.
- W410950918 magId "410950918" @default.
- W410950918 workType "book" @default.