Photooxygenations of 1-naphthols:: an environmentally friendly access to 1,4-naphthoquinones

被引：51

作者：

Suchard, O

Kane, R

Roe, BJ

Zimmerman, E

Jung, C

Waske, PA

Mattay, J

Oelgemöller, M

机构：

[1] Univ Bielefeld, Fak Chem, D-33501 Bielefeld, Germany

[2] Dublin City Univ, Sch Chem Sci, Dublin 9, Ireland

[3] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin 9, Ireland

[4] Univ Cologne, Inst Organ Chem, D-50939 Cologne, Germany

[5] Deutsch Zentrum Luft & Raumfahrt eV, DLR, D-51147 Cologne, Germany

来源：

TETRAHEDRON | 2006年 / 62卷 / 07期

关键词：

photochemistry; photooxygenations; Green chemistry;

D O I：

10.1016/j.tet.2005.11.021

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Dye sensitized photooxygenations of 1-naphthols were investigated with soluble and solid-supported sensitizers and moderate to excellent yields of the corresponding 1,4-naphthoquinones were achieved in relatively short irradiation times. The mild and environmentally friendly reaction conditions made this application particularly attractive for 'Green Pholochemistry'. Consequently, the photooxygenation of 1,5-dihydroxynaphthalene was Studied with non-concentrated and moderately concentrated sunlight and 5-hydroxy-1,4-naphthoquinone (Juglone) was obtained in yields Lip to 71%. (c) 2005 Elsevier Ltd. All rights reserved.

引用

页码：1467 / 1473

页数：7

共 62 条

[21] SOLAR CHEMISTRY - CLASSIFICATION, CRITERIA, AND IDENTIFICATION OF RESEARCH-AND-DEVELOPMENT DEFICITS [J].