Art

J-GLOBAL ID：200902281616469569   Reference number：07A0135155

Oxyfunctionalization Products of Terpenoids with Dimethyldioxirane and Their Biological Activity

ジメチルジオキシランによるテルペノイドのオキシ官能化生成物及びその生物活性

Author (6)： OGAWA Shoujiro (Dep. of Chemistry and ^{b Dep. of General Studies, Coll. of Humanities and Sciences, Nihon University}) ,  HOSOI Keiji (Dep. of Chemistry and ^{b Dep. of General Studies, Coll. of Humanities and Sciences, Nihon University}) ,  IKEDA Noriaki (Dep. of Chemistry and ^{b Dep. of General Studies, Coll. of Humanities and Sciences, Nihon University}) ,  MAKINO Mitsuko ,  FUJIMOTO Yasuo ,  IIDA Takashi (Dep. of Chemistry and ^{b Dep. of General Studies, Coll. of Humanities and Sciences, Nihon University})
Material： Chemical and Pharmaceutical Bulletin  (Chemical & Pharmaceutical Bulletin)
Volume： 55  Issue： 2  Page： 247-250 (J-STAGE)  Publication year： 2007 
JST Material Number： G0504A  ISSN： 0009-2363  CODEN： CPBTAL  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *terpenoid ,...
Semi thesaurus term： bridged compound

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JST classification (2)： Terpenoids in general  (CF10021J) ,  Synthesis of drugs  (GV01030F)

Substance index (20)： Kauralexin A2 ,  11-Oxoursolic acid acetate ,  17-Hydroxy-15α,16α-epoxykaura-18-oic acid ,  Diterpenoid SP-II ,  16-Hydroxy-17-chlorokaurane-18-oic acid ,  17-Hydroxykaur-15-en-18-oic acid ,  3β-Acetoxylupa-20(29)-ene-30-al ,  Lantanone ,  3β-Acetoxy-12α,13-dihydroxyoleanan-28-oic acid γ-lactone ,  3β-Acetoxy-12α,13-dihydroxyoleana-9(11)-ene-28-oic acid 28,13-lactone ,  3β-Acetoxy-12α-chloro-13-hydroxyoleanane-28-oic acid lactone ,  3β-Acetoxy-12β,13-dihydroxyoleana-9(11)-ene-28-oic acid 28,13-lactone ,  3β-Acetoxy-13,20-dihydroxyurs-11-ene-28-oic acid 28,13-lactone ,  O-Acetylursolic acid lactone ,  3β-Acetoxy-30-norlupa-20-one ,  3-O-Acetyloleanolic acid ,  Acetyl ursolic acid ,  Kaurenic acid ,  Dimethyldioxirane ,  Lupeol acetate

Reference (13)：

• 1) Omura T., Ishimura Y., Fujii Y. (eds.), “Cytochrome P-450,” Kodansha, Tokyo, 1993.
• 2) Reese R. B., Steroids, 66, 481—497 (2001).
• 3) Meunier B., Chem. Rev., 92, 1411—1456 (1992).
• 4) Ogawa S., Iida T., Goto T., Mano N., Goto J., Nambara T., Org. Biomol. Chem., 2, 1013—1018 (2004).
• 5) Murry R. W., Chem. Rev., 89, 1187—1201 (1989).

Terms in the title (5)： ジメチルジオキシラン ,  テルペノイド ,  官能化 ,  生成物 ,  生物活性