Reaction Capabilities

1. CHLORINATION

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

2. ALCOHOL TO CHLORIDES

• With Thionyl chloride
• With Hydrochloric acid

3. BROMINATION

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

4. CYANATION

• Halide replacement with cyanide using Sodium cyanide

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

6. REDUCTION

• Ester, ketone, aldehyde reductions with borohydride
• Nitroso reduction with iron / acid and polysulphide
• Imine reduction with borohydride
• Oxime reduction with metal acid

7. OXIDATION

• Alcohols to aldehydes under controlled condition

8. AMIDATION

• Acid / Ester to amides
• Amine formylation

9. HETEROCYCLE SYNTHESIS

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

10. Malonic Ester synthesis.

11. Wittig and Related reactions

12. Phase transfer catalyst + - synthesis and reactions.

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