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Industrial Biotransformations

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1.1 From the “Flower of Vinegar” to Recombinant E. Coli – The History of Microbial <strong>Biotransformations</strong><br />

HO PhCOO<br />

AcO<br />

O<br />

AcO<br />

O<br />

Br<br />

HO<br />

O<br />

O<br />

HO<br />

O 14) tosyl chloride O<br />

O<br />

cortisone acetate<br />

1) PhCOCl<br />

5) HOBr<br />

AcO<br />

HO<br />

HO<br />

PhCOO<br />

O<br />

Br<br />

2) KOH<br />

3) ∆<br />

4) Ac2O 6) CrO 3<br />

19) Ac 2O<br />

20) PBr 3<br />

OH<br />

24) CrO3, KOH<br />

O<br />

25) Ac2O O<br />

OAc<br />

HO<br />

OAc<br />

26) Br2 O<br />

Br<br />

COOCH3 7) Zn<br />

COOCH3 NH2 8) KOH O<br />

11) NaN3 O<br />

9) HOAc<br />

10) SOCl2 12) HOAc<br />

OH<br />

O<br />

COOCH 3<br />

COOCH 3<br />

HO<br />

Br<br />

27) Pyridine<br />

28) K 2CO 3<br />

29) Ac 2O<br />

18) H 2<br />

21) KOAc<br />

22) KOH<br />

23) succinic anhydride<br />

O<br />

O<br />

O<br />

15) O 3<br />

HO<br />

O<br />

OAc<br />

COOCH 3<br />

COOCH 3<br />

O<br />

O<br />

O<br />

30) CrO 3<br />

O<br />

O<br />

HO HO<br />

OAc<br />

O<br />

31) hydrolysis<br />

Fig. 1.10 Chemical synthesis of cortisone.<br />

O<br />

OH<br />

HO<br />

cortisone<br />

13) HNO 3<br />

pyridine<br />

OH<br />

16) KOH<br />

17) C 2H 2<br />

COOH<br />

7

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