Oxidation of 1,5-naphthalenediol and its methyl ether: preparation of juglone methyl ether monoacetal

  title={Oxidation of 1,5-naphthalenediol and its methyl ether: preparation of juglone methyl ether monoacetal},
  author={D. J. Crouse and M. Wheeler and M. Goemann and P. S. Tobin and S. K. Basu and D. Wheeler},
  journal={Journal of Organic Chemistry},
15 Citations
Thallium(III) Nitrate Trihydrate
[13453-38-8] H6N3O12T1 (MW 444.47) InChI = 1S/3NO3.3H2O.Tl/c3*2-1(3)4;;;;/h;;;3*1H2;/q3*-1;;;;+3 InChIKey = ZCPIKMRXMBJLCP-UHFFFAOYSA-N (oxidizing agent; Lewis acid forExpand
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Porphyrins covalently linked to aminomethylated Merrifield polymers, by chlorosulfonation activation of the porphyrin nucleus, are able to generate singlet oxygen with an efficiency which is relatedExpand
Green photochemistry: solar-chemical synthesis of Juglone with medium concentrated sunlight
Dye sensitized photooxygenations of 1,5-dihydroxynaphthalene were investigated with soluble and solid-supported sensitizers and moderately concentrated sunlight. Moderate to good yields up to 79% ofExpand
Photooxygenations of 1-naphthols: an environmentally friendly access to 1,4-naphthoquinones
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 achievedExpand
Green photochemistry: solar photooxygenations with medium concentrated sunlight
The rose bengal sensitized photooxygenations of citronellol and 1,5-dihydroxynaphthalene were performed successfully under solar irradiation conditions, and complete conversions (>95%) were achievedExpand
Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues.
Oxygenated pterocarpans and 5-azapterocarpans are prepared utilizing Lewis acid-promoted reactions of 2-alkoxy-1,4-benzoquinones with 2H-chromenes and N-tosyl-1,2-dihydroquinolines, respectively.Expand
Synthesis of (±)-dihydroxyserrulatic acid via (arene)chromium complexes
Abstract The title compound has been synthesized with high selectivity by utilizing some characteristic properties of (arene)chromium complexes.
Psorolactones and other metabolites from psorospermum glaberrimum
The chemical reactions supporting the structure elucidation of psorolactone A (1), isolated from Psorospermum glaberrimum, are described. The new psorolactone B (5), homoferruginin B (6),Expand