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| Proceso genérico de Síntesis Orgánica | Proceso de tipo específico |
|---|---|
| Acetylation | Acetylchloride, acetic anhydride |
| Acylation | O-Acylation, N-Acylation, Sulfonylation, Friedel-Crafts Acylation. |
| Acid Chloride Handling | Acetyl Chloride. |
| Aldo Condensation | Benzaldehyde |
| Alkylation | N-Alkylation, O-Alkylation, S-Alkylation, Eschweilwer-Clarke react. |
| Amination | Delépine reaction, Reductive Amination. |
| Aromatic Substitution | Aromatic halogenation. |
| Bromination | Bromine. |
| Carbamoylation | Carbon dioxide. |
| Carboxylation | Chlorosulfonic acid. |
| Chloromethylation | Chlorine gas, Phosphorous Oxychloride etc. |
| Chlorosulfonation | Chlorosulfonic acid. |
| Chlorination | Hantsch 1,4 Dihydropyridines Synthesis, Fischer indole synthesis. |
| Etherification | Alkoxide or Aroxide and Alkyl Halide. |
| Esterification | Alcohol and Carboxylic Acid. |
| Elimination | Dehydration, Aromatization. |
| Diels-Alder reaction | Maleic anhydre. |
| Delepine Reaction | Hexamethylene tetramine. |
| Dehydration | Sulfuric Acid, Double-bond formation. |
| Decarboxylation | Sulfuric Acid. |
| Cyclization | Chlorine gas, Phosphorous Oxychloride etc. |
| Freidel Crafts reactions | Aluminium Trichloride. |
| Formylation | Phosphorous Oxychloride |
| Halogenation | Aromatic and Aliphatic Bromination and Chlorinations Acyl Halide formations. |
| Heterocyclic Ring Closure | Hantsch 1,4 Dihydropyridines Synthesis, Fischer Indole synthesis. |
| Hydrogenation | Hydrogen, Catalyst, Rreductive. Amination. Ethylamine. |
| Hydrolysis | Ester hydrolisis, Amide hydrolisis. |
| Iodination | Iodine, Sodium Iodine. |
| Leuckart reaction | Ammonium formate. |
| Mannich Reaction | Paraformaldehyde. |
| Metal Hydride Reductions | Sodium Aluminium Hydride, Sodium Borohydride. |
| Nitration | Nitric Acid and Sulphuric Acid Mixture. |
| Nitrogen Heterocyclics | Indoles, Pyridines, 1,4-Dihydropyridines. |
| Oxidation | Aromatization, Dehydrogenation. |
| Phase Transfer Catalysis | Benzyl Triethylammonium chloride. |
| Pirrole Chemistry | Heterocyclic Substitution. |
| Rearrangement | Baker-Ventakaraman rearrangement, Fries rearrangement Schleyer adamantization |
| Reduction | Acetylchloride, acetic anhydride |
| Reductive amination | Ketones and Aldehydes. |
| Transesterification | Methyl Esters and Higher Alcohols. |
| Saponification | Sodium Hydroxide. |
| Sulfur Chemistry | Thiol formation. Sulfoxide Formation. |
| Vilsmeier-Haack Acylation | Phosphorous oxychloride. |
| Wittig Reaction | Triphenylphosphine. |
