Auftragssynthesen

Organica beherrscht die folgenden Auftragssynthesen:

• Abramovitch- Shapiro
• Acetoacetic Ester synthesis
• Acetylation
• Acylation
• Aldehyde disproportionation
• Alder- Ene reaction
• Aldol condensation
• Algar- Flynn- Oyamada reaction
• Alkoxylation
• Alkylation
• Allan- Robinson reaction
• Amidation
• Amination
• Asymmetric synthesis
• Baker- Venkataraman reaction
• Balz- Schiemann reaction
• Bamberger rearrangement
• Bechamp reduction
• Benzilic acid rearrangement
• Benzoin condensation
• Bischler quinoxaline synthesis
• Bischler- Möhlau indole synthesis
• Bischler- Napieralski reaction
• Blanc cyclization
• Blanc reaction
• Blanc rule
• Brackeen imidazole synthesis
• Bredereck imidazole synthesis
• Bromination
• Bucherer reaction
• Buchwald- Hartwig reactions
• Cannizzaro reaction
• Carbomethilation
• Carboxylation
• Chan- Lam Coupling
• Chiral synthesis
• Chlorination
• Chloromethylation
• Chlorosulfonation
• Ciamician- Dennstedt rearrangement
• Claisen condensation
• Claisen- Schmidt reaction
• Combes quinoline synthesis
• Condensation
• Conrad- Limpach reaction
• Coumarines
• Custom synthesis
• Cyanation
• Cyclysation
• Darzens condensation
• Darzens glycidic ester condensation
• Darzens- Claisen reaction
• Darzens- Nenitzescu alkylation
• Dealkylation
• Decarboxylation
• Dehalogenation
• Dehydratisation
• Delepine reaction
• Dess- Martin oxidation
• Diazotation
• Dieckmann condensation
• Dieckmann cyclization
• Dieckmann reaction
• Doebner reaction
• Doebner- von Miller reaction
• Duff reaction
• Einhorn variation
• Einhorn- Brunner reaction
• Enantiopure chemicals
• Ene reaction
• Eschweiler- Clarke methyIation
• Esterification
• Feist- Benary furan synthesis
• Finkelstein reaction
• Fischer esterification
• Fischer indole synthesis
• Fischer- Speier esterification
• Friedel- Crafts
• Friedel- Crafts acylation
• Friedel- Crafts alkylation
• Friedel- Crafts reaction
• Friedlander quinoline synthesis
• Fries rearrangement
• Gabriel synthesis
• Gabriel- Colman rearrangement
• Gewald aminothiophene synthesis
• Gould- Jacobs reaction
• Gribble reduction
• Grignard reactions
• Grignard reagent
• Guareschi- Thorpe condensation
• Halogenation
• Hantzsch pyrrole synthesis
• Hantzsch synthesis
• Heck reaction
• Hell- Volhard- Zelinski reaction
• Henry reaction
• Heterocycles synthesis
• Hinsberg synthesis of thiophene derivatives
• Horner- Wadsworth- Emmons- Wittig
• Hunsdiecker separation
• Hydroformulation
• Hydrogenation
• Hydroxylation
• Iodonation
• Isomerisation
• Japp- Klingemann reaction
• Kamlet reaction
• Knoevenagel condensation
• Knoevenagel- Doebner condensation
• Knorr pyrazole synthesis
• Knorr pyrrole synthesis
• Knorr quinoline synthesis
• Knorr synthesis
• Kostanecki acylation
• Kostanecki reaction
• Krohnke pyridine synthesis
• Leimgruber- Batcho indole synthesis
• Leuckart reaction
• Leuckart reaction
• Leuckart(-Wallach) reaction
• Lieben haloform reaction
• Lieben iodoform reaction
• Madelung indole synthesis
• Malonic ester synthesis
• Mannich reaction
• Methylation
• Michael addition
• Michael condensation
• Michael reaction
• Morgan- Walls reaction
• Nencki reaction
• Nenitzescu indole synthesis
• Niementowski quinoline synthesis
• Nitration
• Nitrile synthesis
• Nitrosation
• Organometallic reactions
• Oxidation
• Paal- Knorr furan synthesis
• Paal- Knorr pyrrole synthesis
• Pechmann condensation
• Pellizzari reaction
• Perkin reaction (cinnamic acid synthesis)
• Pfitzinger reaction
• Pfitzner- Moffatt oxidation
• Pharmaceutical intermediates
• Pictet- Gams isoquinoline synthesis
• Pictet- Hubert reaction
• Pictet- Spengler isoquinoline synthesis
• Piloty- Robinson pyrrole synthesis
• Piloty- Robinson synthesis
• Pinner reaction
• Pomeranz- Fritsch reaction
• Pschorr arylation
• Quarternization
• Reduction
• Reductive amination
• Reissert indole synthesis
• Resolution of racemates
• Sandmeyer reaction
• Schotten- Baumann reaction
• Scintillation dyes
• Skraup reaction
• Sommelet reaction
• Steglich esterification
• Steglich reaction
• Stereoselective synthesis
• Stobbe condensation
• Sulphonation
• Suzuki coupling
• Swern oxidation
• Thiele reaction
• Thiele- Winter acetoxylation
• Thiele- Winter reaction
• Toll synthesis
• Tosylation
• Vilsmeier- Haack reaction
• Williamson ether synthesis
• Wittig indole synthesis
• Wittig olefination
• Wittig reaction
• Wittig reagents
• Wolff- Kishner reduction
• Yamamoto esterification