The nucleophilic aromatic photosubstitution in photoaffinity labelling. A model study of a cycloheximide derivative.

A. Castelló; J. Marquet; M. Moreno-Mañas; X. Sirera

doi:10.1016/S0040-4039(00)94861-5

The nucleophilic aromatic photosubstitution in photoaffinity labelling. A model study of a cycloheximide derivative.

A. Castelló, J. Marquet, M. Moreno-Mañas, X. Sirera

Departament de Química

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The photoreactions of several 4-nitrocatechol ethers with the relatively hard nucleophile methylamine occurs at the meta position respect to the nitro group. A derivative of the antibiotic cycloheximide carrying a 4-nitrocatechol ether moiety reacts with methylamine affording an in vitro model for photoaffinity labelling. © 1985.

Idioma original	Anglès
Pàgines (de-a)	2489-2492
Revista	Tetrahedron Letters
Volum	26
Número	20
DOIs	https://doi.org/10.1016/S0040-4039(00)94861-5
Estat de la publicació	Publicada - 1 de gen. 1985

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10.1016/S0040-4039(00)94861-5

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title = "The nucleophilic aromatic photosubstitution in photoaffinity labelling. A model study of a cycloheximide derivative.",

abstract = "The photoreactions of several 4-nitrocatechol ethers with the relatively hard nucleophile methylamine occurs at the meta position respect to the nitro group. A derivative of the antibiotic cycloheximide carrying a 4-nitrocatechol ether moiety reacts with methylamine affording an in vitro model for photoaffinity labelling. {\textcopyright} 1985.",

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T1 - The nucleophilic aromatic photosubstitution in photoaffinity labelling. A model study of a cycloheximide derivative.

AU - Castelló, A.

AU - Marquet, J.

AU - Moreno-Mañas, M.

AU - Sirera, X.

PY - 1985/1/1

Y1 - 1985/1/1

N2 - The photoreactions of several 4-nitrocatechol ethers with the relatively hard nucleophile methylamine occurs at the meta position respect to the nitro group. A derivative of the antibiotic cycloheximide carrying a 4-nitrocatechol ether moiety reacts with methylamine affording an in vitro model for photoaffinity labelling. © 1985.

AB - The photoreactions of several 4-nitrocatechol ethers with the relatively hard nucleophile methylamine occurs at the meta position respect to the nitro group. A derivative of the antibiotic cycloheximide carrying a 4-nitrocatechol ether moiety reacts with methylamine affording an in vitro model for photoaffinity labelling. © 1985.

U2 - 10.1016/S0040-4039(00)94861-5

DO - 10.1016/S0040-4039(00)94861-5

M3 - Article

SN - 0040-4039

VL - 26

SP - 2489

EP - 2492

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 20

ER -

The nucleophilic aromatic photosubstitution in photoaffinity labelling. A model study of a cycloheximide derivative.

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