✦ LIBER ✦

Duet electrosynthesis Part II: 1,4-naphthoquinone from naphthalene

✍ Scribed by S. Ito; Y. Kuroda; M. Iwata; K. Sasaki; A. Okazaki

Book ID: 104679755
Publisher: Springer
Year: 1993
Tongue: English
Weight: 629 KB
Volume: 23
Category: Article
ISSN: 0021-891X
DOI: 10.1007/bf00243337

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Electrochemical study of intramolecular

Electrochemical study of intramolecular charge transfer complexes derived from 1,4-naphthoquinone Part 1. Electroreduction

✍ Baiba Turovska; Jānis Stradiņš; Jāzeps Logins; Ivars Strazdiņš; Jānis Drēgeris 📂 Article 📅 1995 🏛 Elsevier 🌐 English ⚖ 748 KB

Electrochemical study of intramolecular

Electrochemical study of intramolecular charge transfer complexes derived from 1,4-naphthoquinone. Part 2. Electro-oxidation of 2-substituted 3-arylamino-1,4-naphthoquinone autocomplexes

✍ Baiba Turovska; Janis Stradinš; Janis Freimanis; Ivars Strazdinš; Jazeps Logins; 📂 Article 📅 1996 🏛 Elsevier 🌐 English ⚖ 535 KB

ChemInform Abstract: 1,4-Naphthoquinones

ChemInform Abstract: 1,4-Naphthoquinones. Part 27. 2-(3-Halogen-4-hydroxyphenyl)-1,4-naphthoquinones from Their 2-(3,5-Di-tert-butyl-4-hydroxyphenyl) Congeners, Potent 5-Lipoxygenase Inhibitors.

✍ G. Wurm; S. Schwandt 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

In vitro toxicity of naphthalene, 1-naph

In vitro toxicity of naphthalene, 1-naphthol, 2-naphthol and 1,4-naphthoquinone on human CFU-GM from female and male cord blood donors

✍ C. Croera; D. Ferrario; L. Gribaldo 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 235 KB

Heterocyclic spiro-naphthalenones. Part

Heterocyclic spiro-naphthalenones. Part IV. Synthesis of some 3,4-dihydrospiro [naphthalene-2(1H),2′-pyrrolidine]-1-ols from 3,4-dihydrospiro [furan-2(5H),1′(2′H)-naphthalene]-2′,5-dione

✍ Daniel Berney; Karlheinz Schuh 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 German ⚖ 317 KB

## Abstract Depending on the experimental conditions the spirolactone **3** on treatment with methylamine gave compounds **6, 7** or the rearranged product **4**. Compound **4** was used to prepare the title compounds **11–13, 15, 18–20** and other derivatives.

Preparation of α-and β-methylnaphthalene

Preparation of α-and β-methylnaphthalene from tar-oil fractions. Part II. α-methyl-naphthalene

✍ Wood, R. ;Wyatt, G. H. 📂 Article 📅 1943 🏛 Wiley (John Wiley & Sons) ⚖ 387 KB

PREPARATION OF a-AND ~-MEl"APHTHAIENE NAPHTHALENE FROM TAR-OIL FRACTIONS. PART II. a-METHYL-, ' Br E. A.COUlSON l'u rui~el~trlu tliu csainiiiiitinii of tlic nietl~yliia~ilitlinlciit~ fnictioiii of ttir oil n coiivenicnt iiictliotl nf ~iil~~lioiintioii-frn~tiiiiinl iIeriilplinnntio:i lips now lmn cla