dc.contributor.author |
Arad-Yellin, R |
en |
dc.contributor.author |
Tsoucaris, G |
en |
dc.contributor.author |
Green, B |
en |
dc.date.accessioned |
2014-06-06T06:44:32Z |
|
dc.date.available |
2014-06-06T06:44:32Z |
|
dc.date.issued |
2001 |
en |
dc.identifier.uri |
http://dx.doi.org/10.1016/S0040-4039(00)02170-5 |
en |
dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1937 |
|
dc.subject |
Chemical Reaction |
en |
dc.subject |
Controlled Release |
en |
dc.subject |
Uv Irradiation |
en |
dc.title |
Reversible encapsulation of guests in modified cyclodextrins: studies with the β-cyclodextrin percinnamate·1,7-dioxaspiro[5,5]undecane system |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/S0040-4039(00)02170-5 |
en |
heal.publicationDate |
2001 |
en |
heal.abstract |
UV irradiation of a solution of the pheromone 1,7-dioxaspiro[5,5]undecane (DU) and β-cyclodextrin percinnamate (β-CD-PC) induces the formation of intramolecular cyclobutane bridges that trap the pheromone within the cyclodextrin cavity. Release of the pheromone can be achieved by bond-breaking chemical reactions, suggesting that such systems may be used for the controlled release of this or other pheromones under field conditions. |
en |
heal.journalName |
Tetrahedron Letters |
en |
dc.identifier.doi |
10.1016/S0040-4039(00)02170-5 |
en |