TY - JOUR
T1 - Reaction mechanism of direct episulfidation of caryophyllene and humulene
AU - Ashitani, Tatsuya
AU - Borg-Karlson, Anna Karin
AU - Fujita, Koki
AU - Nagahama, Shizuo
PY - 2008/4/15
Y1 - 2008/4/15
N2 - Direct episulfidations of caryophyllene or humulene with elemental sulfur were examined by means of gas chromatography. Caryophyllene-6,7-episulfide was formed at an early stage in a reaction of the caryophyllene and elemental sulfur at 120°C. Caryophyllene-3,6-sulfide and polymer compounds were formed after the episulfidation. Formations of the these compounds were related to the disappearance of the caryophyllene-6,7-episulfide. Isomerization from the caryophyllene to isocaryophyllene was also observed during the reaction. In the reaction of humulene with elemental sulfur, humulene-6,7-episulfide was initially produced and then converted to humulene-9,10-episulfide. It was assumed that the polymer compound in the reaction of humulene with sulfur was related to the disappearance of the both humulene episulfides.
AB - Direct episulfidations of caryophyllene or humulene with elemental sulfur were examined by means of gas chromatography. Caryophyllene-6,7-episulfide was formed at an early stage in a reaction of the caryophyllene and elemental sulfur at 120°C. Caryophyllene-3,6-sulfide and polymer compounds were formed after the episulfidation. Formations of the these compounds were related to the disappearance of the caryophyllene-6,7-episulfide. Isomerization from the caryophyllene to isocaryophyllene was also observed during the reaction. In the reaction of humulene with elemental sulfur, humulene-6,7-episulfide was initially produced and then converted to humulene-9,10-episulfide. It was assumed that the polymer compound in the reaction of humulene with sulfur was related to the disappearance of the both humulene episulfides.
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U2 - 10.1080/14786410701591903
DO - 10.1080/14786410701591903
M3 - Article
C2 - 18415856
AN - SCOPUS:42449144620
SN - 1478-6419
VL - 22
SP - 495
EP - 498
JO - Natural Product Research
JF - Natural Product Research
IS - 6
ER -