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Stereochemical course of the dehydrogenation of stereospecifically labelled benzylamines by the amine oxidase from pea seedlings E. Back to tab navigation.

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For reproduction of material from all other RSC journals and books: The enzyme from pea seedlings is readily isolated and is stable; it is now a valuable reagent for assaying the configurational purity of substances which are chiral owing to isotopic substitution at a methylene residue carrying a primary amino-group. Information about reproducing material from RSC articles with different licences is available on our Permission Requests page. This may take some time ryabck load.

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For reproduction of material rybsck PCCP: Previous Article Next Article. R -[ methylene – 2 H 1 ]Benzylamine has been synthesised and its absolute configuration established by degradation to 2 R -[2- 2 H 1 ]glycine.

Go to our Instructions for using Copyright Clearance Center page for details. If you are the author of this article you still need to obtain permission to reproduce the whole article in a third party publication with the exception of reproduction of the whole article in a thesis or dissertation. By incubating the corresponding chiral tritiated benzylamines with the amine oxidase from pea seedlings, it has been shown that the pro – S -hydrogen atom is removed stereospecifically from the methylene group in the oxidative deamination of benzylamine to benzaldehyde.

Jump zenw site search. For reproduction of material from NJC: Authors contributing to RSC publications journal articles, books or book chapters do not need to formally request permission to reproduce material contained in this article provided that the correct acknowledgement is given with the reproduced material.