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2 – 4 October 2007 .
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25 – 27 November 2007


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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