Examples of fused heterocycle nomenclature
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- German Fernandez
- NOMENCLATURE OF CONDENSED HETEROCYCLES
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LATEST NEWS
- Benzene - Problem 16
- azo coupling
- Sandmeyer and Schiemann reactions
- Claisen transposition
- birch reduction
- Side chain oxidation
- The benzylic position
- Aromatic nucleophilic substitution by addition-elimination
- Protection of activated positions
- Reduction of nitro to amino and oxidation of amino to nitro
- Synthesis of 1,2-dicarbonyl compounds
- Synthesis of 1,3-dithianes
- benzoin condensation
- acyloinic condensation
- Knoevenagel condensation
- Michael's addition
- Review of Claisen condensation
- helical molecules
- Rp and Sp notation in planes of chirality
- Ra/Sa notation on chirality axes
- R/S notation in stereogenic centers
- Elements of asymmetry leading to chiral molecules
- Elements of symmetry leading to achiral molecules
- conformational analysis
- Molecular structure
- Phosphines and phosphorus ylides
- Synthesis of 1,3-dithianes. UMPOLUNG reactions
- Thioacetals, hydrolysis and reduction to alkanes
- ylides of sulfur
- Sulphoxide removal WITHOUT
- The Thioethers
- thiols
- simulation of the infrared spectrum of propanamide
- Simulation of the infrared spectrum of 1-butanamine
- Simulation of the infrared spectrum of ethyl ethanoate
- Simulation of the infrared spectrum of ethanoyl chloride
- Simulation of the infrared spectrum of propanoic acid
- Simulation of the infrared spectrum of ethanenitrile
- Simulation of the infrared spectrum of diethyl ether
- Simulation of the infrared spectrum of ethanal
- Simulation of the infrared spectrum of 2-butanone
- Simulation of the infrared spectrum of 1-propanol
- Guareschi-Thorpe synthesis of pyridine
- Kröhnke synthesis of pyridine
- Pomerantz-Fritsch synthesis of isoquinolines
- Pictet Spengler synthesis of isoquinoline
- Bischer–Napieralski synthesis
- Friedlander quinoline synthesis
- Combes synthesis of quinolines
- Alkyl and vinyl quinolines and isoquinolines
- Nucleophilic substitution in quinoline and isoquinoline
- Nucleophilic addition to quinolines and isoquinolines
- Lithiation reaction in quinoline and isoquinoline
- Electrophilic substitution by N-oxides
- Electrophilic substitution reaction in quinoline and isoquinoline
- Reactions with nitrogen lone pair: quinoline and isoquinoline
- Reactivity of alkyl and vinyl pyridines
- Nucleophilic substitution by elimination-addition: the pyridine
- Nucleophilic substitution reactions in pyridine
- Nucleophilic addition reactions to pyridines
- pyridine lithiation
- Electrophilic substitution at position 4 of pyridine
- Synthesis of thiophene by 1,3-dipolar
- Paal–Knorr synthesis of thiophene
- Furan synthesis by 1,3-dipolar
- Feist-Benary synthesis of furan
- Paal–Knorr synthesis of furans
- Synthesis of pyrrole via 1,3-dipolar
- Hantzch synthesis of pyrrole
- Paal–Knorr synthesis of pyrrole
- furan opening
- Derivatives of pyrrole, thiophene and furan
- Cycloaddition reactions in furan
- Lithiation reaction
- Nucleophilic substitution in pyrrole, thiophene and furan
- nucleophilic addition
- Electrophilic substitution on thiophene
- Sulfonation, formylation, Mannich and acetylation of furan
- Madelung synthesis of indole
- Fisher's synthesis of indole
- Indole ring reduction
- Indole ring expansion
- Indole derivatives
- Electrophilic substitution with position 3 of the indole occupied
- Electrophilic substitution at the indole
- indole acidity
- Examples of fused heterocycle nomenclature
- Literation of the base heterocycle and numbering of the annex
- Peripheral numbering of the global heterocycle
- Rules for the choice of the base component
- General concepts of condensed heterocycle nomenclature
- General characteristics of diazines
- Cyclization of carbenes nitrenes and radicals
- Cyclization on sp carbons
- Cyclization processes by nucleophilic addition and addition-elimination at sp¹²2 carbons
- Formation of cycles through S$_N$2
- Classification of nucleophilic attacks (Baldwin's Rules)
- Reactants in cyclization reactions
- Synthesis of heterocycles by cyclization reactions
- The anomeric effect