The enantioselective first total synthesis of (R)-(-)-pyridindolol K2(2) together with its enantiomer (2a) has been achieved in nine steps.Pyridindolol K2 (2) was isolated from the culture broth of Streptomyces sp.K93-0711 together with pyridindolol K1 (1) and pyridindolol (3) in 1997 by Omura and co-workers. 1 Pyridindolol (3) is already known to be a β-galactosidase inhibitor, 2 and pyridindolol glucosides have also been isolated from
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Hibino et al. (2000) studied this question.
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