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Open Access
Orthoamide, LXIII [1]. Tris(dichlormethyl)amin, ein neues breit anwendbares Formylierungsmittel für Aromaten / Orthoamides, LXIII [1]. Tris(dichloromethyl)amine, a New Formylating Reagent for Aromatic Compounds of Wide Scope
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Willi Kantlehner
, Ralf Kreß
Published/Copyright:
June 2, 2014
Received: 2006-1-25
Published Online: 2014-6-2
Published in Print: 2006-4-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
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- Two-Carbon Ring Enlargement of Five-, Six-, and Seven-Membered 1-Aza-2-vinylcycloalk-2-enes with Dimethyl Acetylenedicarboxylate and Subsequent Thermal Isomerization Reactions
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- Synthesis of 5-Methoxy-4-benzyloxazoles from Tyrosine and m-Tyrosine under Bischler-Napieralski Conditions
- Palladium-Catalyzed Coupling Reaction of 3-Bromo Benzo[b]furan, -thiophene and -selenophene 2-Carboxaldehyde. Preparation of Tetracyclic Heteroaromatic Derivatives
- Introduction of Substituents on the 2-Oxo-piperazine Skeleton by [3+2] Cycloaddition and Subsequent Transformation
- Syntheses and Properties of Cycloamidines Based on 4H-Imidazoles
- Orthoamide, LXIII [1]. Tris(dichlormethyl)amin, ein neues breit anwendbares Formylierungsmittel für Aromaten / Orthoamides, LXIII [1]. Tris(dichloromethyl)amine, a New Formylating Reagent for Aromatic Compounds of Wide Scope
- Synthesis of N,N’-Linked Isothiazolium Salts via Intramolecular Cyclocondensation of Hydrazonium Salts
- Bromocyclization of Unsaturated Oximes. Synthesis of Five-Membered Cyclic Nitrones (Pyrroline N-Oxides)
- Two-Step Synthetic Approach to 6-Substituted Pyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones from 6-Amino-, 6-Alkylamino-, and 6-Arylamino-1,3-dimethyluracils
Keywords for this article
Tris(dichloromethyl)amine;
Aromatic Aldehydes;
Formylation;
Electrophilic Aromatic Substitution
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BY-NC-ND 3.0
Articles in the same Issue
- Synthesis and Properties of Thiamethoxam and Related Compounds
- Monocyclische und spirocyclische Boronium-Verbindungen: Altes und Neues von einer bisher weitgehend unbeachteten Stoffklasse / Monocyclic and Spirocyclic Boronium Compounds – Old and New Aspects of a Hitherto Rather Disregarded Class of Substances
- Physical, Chemical, and Technological Property Correlation with Chemical Structure: The Potential of QSPR
- Two-Carbon Ring Enlargement of Five-, Six-, and Seven-Membered 1-Aza-2-vinylcycloalk-2-enes with Dimethyl Acetylenedicarboxylate and Subsequent Thermal Isomerization Reactions
- Syntheses and Properties of Di- and Tricationic Hetarenium-Substituted Pyrimidines
- Nucleoside Analogues from Push-Pull Functionalized Branched-Chain Pyranosides
- Synthesis and Transformations of Ethyl 3-Formyl-1H-indole-2-carboxylate. Preparation of Aplysinopsin and β-Carboline Thiohydantoin Analogues
- Synthesis of 5-Methoxy-4-benzyloxazoles from Tyrosine and m-Tyrosine under Bischler-Napieralski Conditions
- Palladium-Catalyzed Coupling Reaction of 3-Bromo Benzo[b]furan, -thiophene and -selenophene 2-Carboxaldehyde. Preparation of Tetracyclic Heteroaromatic Derivatives
- Introduction of Substituents on the 2-Oxo-piperazine Skeleton by [3+2] Cycloaddition and Subsequent Transformation
- Syntheses and Properties of Cycloamidines Based on 4H-Imidazoles
- Orthoamide, LXIII [1]. Tris(dichlormethyl)amin, ein neues breit anwendbares Formylierungsmittel für Aromaten / Orthoamides, LXIII [1]. Tris(dichloromethyl)amine, a New Formylating Reagent for Aromatic Compounds of Wide Scope
- Synthesis of N,N’-Linked Isothiazolium Salts via Intramolecular Cyclocondensation of Hydrazonium Salts
- Bromocyclization of Unsaturated Oximes. Synthesis of Five-Membered Cyclic Nitrones (Pyrroline N-Oxides)
- Two-Step Synthetic Approach to 6-Substituted Pyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones from 6-Amino-, 6-Alkylamino-, and 6-Arylamino-1,3-dimethyluracils