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- W4298367779 abstract "Synthetic routes to tyramine have been developed which allow stereoselective labelling with isotopic hydrogen at C-2 in configurations established by chemical correlation with [2-2H1]succinic acid of known absolute configuration. The various labelled tyramines have been converted into samples of O-methylnorbelladine [as (33)] which are used to prove that the hydroxylation step at saturated carbon in haemanthamine biosynthesis occurs (a) stereo-specifically with removal of the pro-R hydrogen atom and (b) with retention of configuration." @default.
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- W4298367779 date "1973-01-01" @default.
- W4298367779 modified "2023-09-26" @default.
- W4298367779 title "Studies of enzyme-mediated reactions. Part III. Stereoselective labelling at C-2 of tyramine: stereochemistry of hydroxylation at saturated carbon" @default.
- W4298367779 doi "https://doi.org/10.1039/p19730001609" @default.
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