Art

J-GLOBAL ID：200902204681609012   Reference number：08A1072396

Efficient Synthesis of a New L-Shaped Dimer of Naphthalene, and Its Analogs

ナフタレンの新規L形二量体,およびその類似体の効率的合成

Author (5)： YOSHIOKA Ken (Div. of Applied Bioscience, Graduate School of Agriculture, Hokkaido Univ.) ,  TAKAISHI Izumi (Div. of Applied Bioscience, Graduate School of Agriculture, Hokkaido Univ.) ,  SHIOZAWA Kazunari (Mitsui Chemical Analysis and Consulting Serv., Inc.) ,  FUKUSHI Yukiharu (Div. of Applied Bioscience, Graduate School of Agriculture, Hokkaido Univ.) ,  TAHARA Satoshi (Div. of Applied Bioscience, Graduate School of Agriculture, Hokkaido Univ.)
Material： Bioscience, Biotechnology, and Biochemistry  (Bioscience Biotechnology & Biochemistry)
Volume： 72  Issue： 10  Page： 2632-2639 (J-STAGE)  Publication year： 2008 
JST Material Number： G0021A  ISSN： 0916-8451  CODEN： BBBIEJ  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *polynuclear aromatic compound ,  *dimer ,  chemical synthesis ,  reaction mechanism ,  Friedel-Crafts reaction ,  cyclization reaction ,  anisotropy ,  optical isomerism ,  analytical reagent ,  *Naphthalenes ,  axial chirality
Semi thesaurus term： L形二量体

JST classification (1)： Naphthalenes  (CF06020D)

Substance index (4)： 14H-Dinaphtho[1,8-bc:1′,8′-fg]oxocin-14-one ,  2,2′-Spirobi[2H-naphtho[1,8-bc]furan] ,  7H-14-Oxabenzo[k]pleiadene-7-one ,  7H-Dibenzo[c,h]xanthen-7-one

Reference (14)：

• 1) Seco, J. M., Quiñoá, E., and Riguera, R., The assignment of absolute configuration by NMR. Chem. Rev., 104, 17–117 (2004).
• 2) Fukushi, Y., Yajima, C., and Mizutani, J., A new method for establishment of absolute configurations of secondary alcohols by NMR spectroscopy. Tetrahedron Lett., 35, 599–602 (1994).
• 3) Fukui, H., Fukushi, Y., and Tahara, S., NMR determination of the absolute configuration of cyclic chiral alkenes. Tetrahedron Lett., 40, 325–328 (1999).
• 4) Fukui, H., Fukushi, Y., and Tahara, S., NMR determination of the absolute configuration of chiral 1,2- and 1,3-diols. Tetrahedron Lett., 44, 4063–4065 (2003).
• 5) Terajima, M., Cai, J., and Lim, E. C., Time-resolved RPR and optical studies of intermoiety interaction in the lowest triplet state of L-shaped dimers of naphthalene. J. Phys. Chem. A, 104, 1662–1669 (2000).

Terms in the title (4)： ナフタレン ,  L形 ,  二量体 ,  類似体