Issue 11, 1997

Microbiological Transformations. Part 14.1 Microbiological Transformations of Derivatives and Open-chain Analogues of 1,2,3,4-Tetrahydroisoquinoline with the Fungus Cunninghamella elegans

Abstract

Incubation of N-benzoyl- and 1-methyl-N-benzoyl-1,2,3,4-tetrahydroisoquinolines with the mycelium of the fungus Cunninghamella elegans results in both benzylic hydroxylation and the formation of phenolic products; the 2- and 3-methyl substituted analogues gave products arising from C-1 hydroxylation.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 381-381

Microbiological Transformations. Part 14.1 Microbiological Transformations of Derivatives and Open-chain Analogues of 1,2,3,4-Tetrahydroisoquinoline with the Fungus Cunninghamella elegans

L. M. Canfield and T. A. Crabb, J. Chem. Res. (S), 1997, 381 DOI: 10.1039/A701376K

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