Suzuki, Heck and Sonogashire Couplings
Chiral Heterocyclic Transformations
Protections of Amino Acids and their Derivatives (Fmoc-, Boc-)
Liquid Phase Peptide Synthesis
Freidel-Crafts Acylation and Alkylation
Thiophosgenation and Phosgenation
Fluorination, Bromination and Iodination
Acetoacetylation and Acrylation
Amidation and Amination
Azidation, Carbonylation and Carboxylation
Cyanomethylation and Cyclization
Diketene and Ketene Reactions
Epichlorohydrin Chemistry and Epoxidation
Hydrazine Chemistry and Reactions
Hydroformylation and Hydrosilylation
Nitromethylation and Nitrosation
Olefin Metathesis
Optically Active Cyanohydrin
Para- and Ortho-Methylation
Peroxidation and Silylations
Sulfochlorination, Sulfonation and Sulfoxidation
Thiocarbonylation and Tosylation
Transamination and Transesterification
Rich experience and innovative research team:
61 project personnel, including 6 doctors, 16 masters and 49 bachlors
Advanced infrastructure and equipments:
7000 FT2 experimental plot, 35 laboratories
Equipped with many sets of analysis and testing equipment: 2 Bruker NMRs, Shimadzu LC/MS, and Shimadzu HPLCs etc.
Production capacity:
In our production base, there is QA, multi-functional laboratory, high-pressure workshop and manufacturing workshop. In multi-functional laboratory, there is 100ml to 50L glass reactor to provide products from gram degree to kilogram degree. In high-pressure workshop, there is 1L to 500L stainless steel high-pressure reactions till. In manufacturing workshop, there is reaction still in glass lining, stainless steel and lining FEFLON, ranging from 100L to 3000L, with total capacity of 52720L to meet requirements of different chemicals and reactions.
Our company has rich experience in following unit reaction: nitration, reduction, diazotization, hydrogenation, halogenations, Grignard, fluorination, cyaniding, hydrolysis, deamination, alkylate, acylation, oxidizing reaction
Key chemical technique platform:
| Aldo condensation | Baeyer -Villiger oxidation |
| Birch reduction | Claisen condensation |
| Curtius | Dieckmann cyclization |
| Diels-Alder | Doebner-Knoevenagel condensation |
| Freidel-Crafts acylation | Freidel-Crafts reaction |
| Fries rearrangement | Gabriel synthesis |
| Gomberg-Bachmann reaction | Grignard reaction |
| Heck reactions | Hoesch, Japp-Klingemann Perking |
| Hoffman degradation | Hofmann’s reaction |
| Mannich reaction | Michael addition |
| Mitsunubo reaction | Reformatsky reaction |
| Ritter reaction | Rosenmund reduction |
| Sandmeyer reaction | Schiff base reduction |
| Schotten-Baumann reaction | Skraup synthesis |
| Strecker amino acid synthesis | Sugasawa reaction |
| Suzuki & Sonogashire coupling | Suzuki reaction |
| Suzuki/Heck coupling | Swern oxidation |
| Ullman reaction | Vilsmeier-Haack reactions |
| Wilgerodt reaction | Williamson synthesis |
| Wittig reaction |
