Solid state photochemistry of ternary cyclodextrin complexes: Total selectivity in the photoreduction of nitrophenyl ethers by 1-phenylethylamine

Miquel Mir; Jorge Marquet; Eduard Cayón

doi:10.1016/S0040-4039(00)60931-0

Solid state photochemistry of ternary cyclodextrin complexes: Total selectivity in the photoreduction of nitrophenyl ethers by 1-phenylethylamine

Miquel Mir, Jorge Marquet, Eduard Cayón

Department of Chemistry

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

19 Citations (Scopus)

Abstract

The irradiation of the ternary complexes of β-cyclodextrin with several nitrophenyl ethers, and 1-phenylethylamine in the solid state, produces selective photoreduction to the corresponding nitroso derivatives. © 1992.

Original language	English
Pages (from-to)	7053-7056
Journal	Tetrahedron Letters
Volume	33
Issue number	46
DOIs	https://doi.org/10.1016/S0040-4039(00)60931-0
Publication status	Published - 10 Nov 1992

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title = "Solid state photochemistry of ternary cyclodextrin complexes: Total selectivity in the photoreduction of nitrophenyl ethers by 1-phenylethylamine",

abstract = "The irradiation of the ternary complexes of β-cyclodextrin with several nitrophenyl ethers, and 1-phenylethylamine in the solid state, produces selective photoreduction to the corresponding nitroso derivatives. {\textcopyright} 1992.",

author = "Miquel Mir and Jorge Marquet and Eduard Cay{\'o}n",

year = "1992",

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AU - Cayón, Eduard

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N2 - The irradiation of the ternary complexes of β-cyclodextrin with several nitrophenyl ethers, and 1-phenylethylamine in the solid state, produces selective photoreduction to the corresponding nitroso derivatives. © 1992.

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