THE FORMATION OF 2-HYDROXYBUT-3-ENYL CYANIDE FROM (2S)-2-HYDROXYBUT-3-ENYL GLUCOSINOLATE USING IMMOBILIZED MYROSINASE

Authors
LEONI O FELLUGA F PALMIERI S
Citation
O. Leoni et al., THE FORMATION OF 2-HYDROXYBUT-3-ENYL CYANIDE FROM (2S)-2-HYDROXYBUT-3-ENYL GLUCOSINOLATE USING IMMOBILIZED MYROSINASE, Tetrahedron letters, 34(49), 1993, pp. 7967-7970
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
49
Year of publication
1993
Pages
7967 - 7970
Database
ISI
SICI code
0040-4039(1993)34:49<7967:TFO2CF>2.0.ZU;2-J
Abstract
Starting from (2S)-2-hydroxybut-3-enylglucosinolate (epi-progoitrin) i solated from Crambe abyssinica seeds the chiralic 2-hydroxy-3-butenyl cyanide was produced in pure form and acceptable yield, using immobili zed myrosinase purified from Sinapis alba on a Nylon 6.6 membrane.