Photooxygenations of 1-naphthols: an environmentally friendly access to 1,4-naphthoquinones
Suchard, Oliver, Kane, Ronan, Roe, Bernard J., Zimmermann, Elmar, Jung, Christian, Waske, Prashant A., Mattay, Jochen, and Oelgemöller, Michael (2006) Photooxygenations of 1-naphthols: an environmentally friendly access to 1,4-naphthoquinones. Tetrahedron, 62 (7). pp. 1467-1473.
|PDF (Published Version) - Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader|
View at Publisher Website: http://dx.doi.org/10.1016/j.tet.2005.11....
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 Photochemistry’. 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 up to 71%.
|Item Type:||Article (Refereed Research - C1)|
|Keywords:||Quinones; Photochemistry; Photooxygenations; Green chemistry|
|FoR Codes:||03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030503 Organic Chemical Synthesis @ 100%|
|SEO Codes:||97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 100%|
|Deposited On:||16 Apr 2010 11:40|
|Last Modified:||29 Jul 2013 00:56|
Last 12 Months: 0
|Citation Counts with External Providers:|
Repository Staff Only: item control page