Literature DB >> 18415856

Reaction mechanism of direct episulfidation of caryophyllene and humulene.

Tatsuya Ashitani1, Anna-Karin Borg-Karlson, Koki Fujita, Shizuo Nagahama.   

Abstract

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 degrees 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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Year:  2008        PMID: 18415856     DOI: 10.1080/14786410701591903

Source DB:  PubMed          Journal:  Nat Prod Res        ISSN: 1478-6419            Impact factor:   2.861


  1 in total

1.  Activity studies of sesquiterpene oxides and sulfides from the plant Hyptis suaveolens (Lamiaceae) and its repellency on Ixodes ricinus (Acari: Ixodidae).

Authors:  T Ashitani; S S Garboui; F Schubert; C Vongsombath; I Liblikas; K Pålsson; A-K Borg-Karlson
Journal:  Exp Appl Acarol       Date:  2015-09-18       Impact factor: 2.132

  1 in total

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