TRANSFORMATION OF 1,2,5,6-TETRAHYDROPYRIDINES WITH MYCELLAR FUNGI
Keywords:
piperidinediol, 1,2,5,6-tetrahydropyridine, mycellar fungi, biotransformation, hydroxylationAbstract
It has been shown that on biotransformation of a series of 1,2,5,6-tetrahydropyridines with strains of the mycellar fungi Cunninghamella verticillata VKPM F-430, Beauveria bassiana ATCC 7159, and Penicillium simplicissimum KM-16, the culture of Cunninghamella verticillata possesses the greatest transforming activity and selectivity. With the aid of the latter practically quantitative oxidation of 1,2,5,6-tetrahydropyridines occurs into the corresponding trans-diol. The structure and spatial disposition of trans-1-benzyl-3,4-dihydroxypiperidine was demonstrated by data of chromato-mass spectrometric analysis and high resolution NMR spectra and was confirmed by comparison with an authentic sample obtained by an alternate synthesis using the oxidation of 1-benzyl-1,2,5,6-tetrahydropyridine with trifluoroperacetic acid.
How to Cite
Terentiev, P. B.; Zilberstein, T. M.; Borisenko, A. A.; Shmorgunov, V. A.; Piskunkova, N. F.; Grishina, G. V. Chem. Heterocycl. Compd. 2003, 39, 885. [Khim. Geterotsikl. Soedin. 2003, 1027.]
For this article in the English edition, see DOI https://doi.org/10.1023/A:1026142220384