The formation of 2-hydroxybut-3-enyl cyanide from (2S)-2-hydroxybut-3-enyl glucosinolate using immobilized myrosinase
1993
Leoni, O. | Felluga, F. | Palmieri, S.
Starting from (2S)-2-hydroxybut-3-enylglucosinolate (epi-progoitrin) isolated from Crambe abyssinica seeds the chiralic 2-hydroxy-3-butenyl cyanide was produced in pure form and acceptable yield, using immobilized myrosinase purified from Sinapis alba on a Nylon 6.6 membrane.
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Bibliographic information
Publisher
American Chemical Society
Other Subjects
Thioglucosidase
Language
English
Type
Journal Article; Text
2024-02-29
MODS
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