MOEHS

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