Reversible encapsulation of guests in modified cyclodextrins: Studies with the β-cyclodextrin percinnamate·1,7-dioxaspiro[5,5]undecane system

Rina Arad-Yellin; George Tsoucaris; Bernard S. Green

doi:10.1016/S0040-4039(00)02170-5

Reversible encapsulation of guests in modified cyclodextrins: Studies with the β-cyclodextrin percinnamate·1,7-dioxaspiro[5,5]undecane system

Rina Arad-Yellin^*, George Tsoucaris, Bernard S. Green

^*Corresponding author for this work

Faculty of Medicine

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

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.

Original language	English
Pages (from-to)	1335-1337
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	7
DOIs	https://doi.org/10.1016/S0040-4039(00)02170-5
State	Published - 12 Feb 2001

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title = "Reversible encapsulation of guests in modified cyclodextrins: Studies with the β-cyclodextrin percinnamate·1,7-dioxaspiro[5,5]undecane system",

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.",

author = "Rina Arad-Yellin and George Tsoucaris and Green, \{Bernard S.\}",

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AU - Arad-Yellin, Rina

AU - Tsoucaris, George

AU - Green, Bernard S.

PY - 2001/2/12

Y1 - 2001/2/12

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/0035847517

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Reversible encapsulation of guests in modified cyclodextrins: Studies with the β-cyclodextrin percinnamate·1,7-dioxaspiro[5,5]undecane system

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