成功研发了一种与已报道的方法相比合成蒽醌衍生物产量更高的新方法,该方法具有原料易得,收率高,反应时间短,反应条件温和以及操作容易等特点. 合成的蒽醌衍生物的结构由物性数据和光谱结果确定.
参考文献
[1] | Thomson R H.Naturally Occurring Quinones[M].London:Buttetworths,1957:309. |
[2] | Fieser L F;Fieser M.Advanced Organic Chemistry[M].New York:Reinhold,1961:845. |
[3] | Fieser L F;Fieser M.Topics in Organic Chemistry[M].New York:Reinhold,1963 |
[4] | Valderrama J A;Gonza′lez M F;Pessoa-Mahana D;Tapia R A Fillion H Pautet F Rodriguez J A Theoduloz C Schmeda-Hirschmann G .[J].Bioorganic and Medicinal Chemistry Letters,2006(14):5003. |
[5] | Shi YQ;Fukai T;Sakagami H;Kuroda J;Miyaoka R;Tamura M;Yoshida N;Nomura T .Cytotoxic and DNA damage-inducing activities of low molecular weight phenols from rhubarb.[J].Anticancer Research: International Journal of Cancer Research and Treatment,2001(4A):2847-2853. |
[6] | Sittie AA;Lemmich E;Olsen CE;Hviid L;Kharazmi A;Nkrumah FK;Christensen SB .Structure-activity studies: in vitro antileishmanial and antimalarial activities of anthraquinones from Morinda lucida (letter)[J].Planta medica: Natural products and medicinal plant research,1999(3):259-261. |
[7] | Rath G;Ndonzao M;Hostettmann K .[J].International Journal of Pharmacognosy,1995,33(02):107. |
[8] | Younos C;Rolland A;Fleurentin J;Lanhers M Misslin R Mortier F .[J].Planta Medica,1990,56(05):430. |
[9] | Adwankar M K;Chitnis M P .[J].Chemotherapy,1982,28(04):291. |
[10] | Koumaglo K;Gbeassor M;Nikabu O;de Souza C Werner W .[J].Planta Medica,1992,58(06):533. |
[11] | Tripathi Y B;Sharma M;Manickam M .[J].Indian Journal of Biochemistry and Biophysics,1997,34(03):302. |
[12] | Chang P;Chen C .[J].Chin Pharm J (Taipei),1995,47(04):347. |
[13] | Ismail NH;Ali AM;Aimi N;Kitajima M;Takayama H;Lajis NH .Anthraquinones from Morinda elliptica.[J].Phytochemistry,1997(8):1723-1725. |
[14] | Patai S.[A].New York:Wiley-Interscience,1988:1019. |
[15] | Tisler M.[M].London,UK:Academic Press,1989:37. |
[16] | Piro B;Pham M C;Bazzaoui E A;Hedayatullah M Lacroix J C Lacaze P C Novák P Haas O .[J].Journal De Chimie Physique Et De Physico-chimie Biologique,1998,95(06):1522. |
[17] | Piro B;Bazzaoui E A;Pham M C;Novák P Haas O .[J].Electrochimica Acta,1999,44(12):1953. |
[18] | Fieser L F .[J].Organic Syntheses Collective,1941,1:353. |
[19] | Clar E .[J].Chemische Berichte,1948,81(01):63. |
[20] | Clar E.[J].Journal of the Chemical Society,1949:2440. |
[21] | Clar E .[J].Chemische Berichte,1948,81(02):169. |
[22] | Uhlig F;Snyder H R .[J].Advances in Organic Chemistry,1960,1:51. |
[23] | Horii Z;Hakusui H;Momose T .[J].Chemical and Pharmaceutical Bulletin,1968,16:1262. |
[24] | Horii Z;Momose T;Tamura Y .[J].Chemical and Pharmaceutical Bulletin,1965,13:797. |
[25] | Dhruba B R;Patil V B;Rama Rao A V .[J].Indian Journal of Chemistry,1976,14B:622. |
[26] | Kozlov V V;Belov B I .[J].Zhurnal Organicheskoi Khimii,1959,29:3450. |
[27] | Perkin A G;Hummel J J .[J].Journal of the Chemical Society,1893,63:1159. |
[28] | Perkin A G;Hummel J J .[J].Journal of the Chemical Society,1895,67:817. |
[29] | Rodgman A .[J].Journal of Organic Chemistry,1959,24(12):1916. |
[30] | Grandmougin E;Hebd C R .[J].Seances Acad Sci,1921,173:1176. |
[31] | Groggins P H;Newton H P .[J].Industrial and Engineering Chemistry,1929,21(04):369. |
上一张
下一张
上一张
下一张
计量
- 下载量()
- 访问量()
文章评分
- 您的评分:
-
10%
-
20%
-
30%
-
40%
-
50%