Reaction Capabilities

1. CHLORINATION :

• Nuclear chlorination with Chlorine gas.
• Nuclear chlorination with Sulphuryl chloride.

6. REDUCTION :

• Ester, ketone, aldehyde reductions with borohydride.
• Nitroso reduction with iron / acid and polysulphide.
• Imine reduction with borohydride.
• Oxime reduction with metal acid.
• Catalytic hydrogenation using Pdlc.

2. ALCOHOL TO CHLORIDES :

• With Thionyl chloride.
• With Hydrochloric acid

7. OXIDATION :

• Alcohols to aldehydes under
  controlled condition.

3. BROMINATION :

• Nuclear bromination with Liquid bromine.
• Side chain bromination with N-Bromosuccinimide.

8. AMIDATION :

• Acid / Ester to amides.
• Amine formylation

4. CYANATION :

• Halide replacement with cyanide using Sodium cyanide.

9. HETEROCYCLE SYNTHESIS :

• Oxazoles
• Purines / Xanthines
• Pyrimidines
• Benzisoxazoles
• Oxadiazoles
• Benzothiazoles

5. ALKYLATION :

• N-Alkylation with dialkyl sulphate and alkyl halides.
• O-Alkylation with dialkyl sulphate and alkyl halides.
• S-Alkylation with alkyl halides.
• C-Alkylation with dialkyl sulphate and alkyl halides.

10. MALONIC ESTER SYNTHESIS

11. WITTIG AND RELATED REACTIONS

12. PHASE TRANSFER CATALYST + SYNTHESIS AND REACTIONS

13. QUARTERNARY HYDROXIDE SYNTHESIS

14. FISCHER OXAZOLE SYNTHESIS

15. GRIGNARD

16. VILSEMEIER HAACK

17. HYDROGENATION