期刊文献+

1,2,3-O-三乙酰基-5-脱氧-D-呋喃核糖的合成研究 被引量:3

Synthesis of 1,2,3-tri-O-acetyl-5-deoxy-D-ribofuranose
下载PDF
导出
摘要 以D-核糖为原料,经过酯化、碘化、还原、水解和乙酰化等步骤合成标题化合物,并探索了一种成本低廉的5位脱氧方法。反应总收率为14.9%。 D-Ribose,as the starting material,was subjected to esterification,iodination,reduction by Raney Ni,hydrolysis and acylation to give 1,2,3-tri-O-acetyl-5-deoxy-D-ribofuranose in an overall yield of 14.9%,leading to the development of a cheap method for deoxygenation of C5.
作者 宋凯 郑国钧
出处 《化学试剂》 CAS CSCD 北大核心 2010年第2期171-172,共2页 Chemical Reagents
关键词 1 2 3-O-三乙酰基-5-脱氧-D-呋喃核糖 抗癌药 中间体 1 2 3-tri-O-acetyl-5-deoxy-D-ribofuranose anticancer drug intermediate
  • 相关文献

参考文献7

  • 1FEI Xiang-shu, WANG Ji-quan, MILLER K D. Synthesis of [18F] Xeloda as a novel potential PET radiotracer for imaging enzymes in cancers [J]. Nucl. Med. Biol., 2004, 31 (8) : 1 033-1 041.
  • 2SAIRAM P,PURANIK R, RAO B S. Synthesis of 1,2,3-tri-O-acetyl-5-deoxy-D-ribofuranose from D-ribose[J]. Garbohydr Res . , 2003,338(4) : 303-306.
  • 3董辉,钱红.去氧氟尿苷合成工艺改进[J].中国医药工业杂志,2002,33(3):108-110. 被引量:14
  • 4GHOSH A K, LIU Wen-ruing. Total synthesis of(+)-sinefungin[J]. J. Org. Chem., 1996,61(18) :6 175-6 182.
  • 5KISSSTAN H M, BAKER B R. The synthesis of certain 5-deoxy- D - ribofuranosylpurine [ J ]. J, Am. Chem. Soc. , 1957,79 (20) :5 534-5 540.
  • 6李志裕,车文军,尤启冬.卡培他滨的合成[J].中国医药工业杂志,2008,39(11):804-807. 被引量:16
  • 7SHI Zhen-dan,YANG Bing-hui,WU Yu-lin. A stereospecific synthesis of L-deoxyribose, L-ribose and L-ribosides [ J ]. Tertrahedron, 2002,58 (16) : 3 287-3 296.

二级参考文献18

  • 1黄海欣,陈绍俊,黄东宁,李桂生.周剂量多西他赛联合卡培他滨治疗晚期胃癌的临床观察[J].中华肿瘤防治杂志,2008,15(9):705-706. 被引量:2
  • 2Kissman HM, Baker BR. The synthesis of certain 5-deoxy- D-ribofuranosylpurines [J]. J Am Chem Soc, 1957, 79 (20): 5534-5540.
  • 3Gosh AK, Liu W. Total synthesis of (+)-sinefungin[J]. J Org Chem, 1996, 61 (18) : 6175-6182.
  • 4Lerner LM. Preparation of 9- (5-deoxy-α-D-arabinofuranosyl)adenine from D-ribose [J]. J Org Chem, 1978, 43 (1) : 161-162.
  • 5Lemer LM. Enantionieric forms of 9- (5-deoxy-β-erythropent-4-enofuranosyl) adenine and a new preparation of 5-deoxy-D-lyxose [J]. Carbohydr Res, 1977, 53: 177-185.
  • 6Lopez-Herrera FJ. The preparation of 7-deoxy-2-deamino-6- hydroxy tunicamine and related products [J]. Tetrahedron, 1996, 52 (13):4757-4768.
  • 7Sairam P, Puranik R. Synthesis of 1,2,3-tri-O-acetyl-5- deoxy-D-ribofuranose from D-ribose [J]. Carbohydr Res, 2003, 338 (4) : 303-306.
  • 8Shunk CH, Lavigne JB, Folkers K. Studies on carcinolytic compounds. V. 6,7-Dimethyl-9- [ 1'- (5-desoxy-D-ribityl) ] - isoalloxazine [J]. J Am Chem Soc, 1955, 77 (8): 2210-2212.
  • 9Fei XS, Wang JQ. Synthesis of [^18F]Xeloda as a novel potential PET radiotracer for imaging enzymes in cancers [J]. Nucl Med Biol, 2004, 31 (8): 1033-1041.
  • 10Shimma N, Umeda I. The design and synthesis of a new tumor-selective fluoropyrimidine carbamate, capecitabine [J]. Bioorg Med Chem, 2000, 8 (7) : 1697-1706.

共引文献25

同被引文献28

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部