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胆酸衍生物的合成及其应用 被引量:5

Syntheses and Applications of Bile Acid Derivatives
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摘要 综述了胆酸衍生物,包括应用于高分子材料、分子识别及医药领域的胆酸衍生物的合成。参考文献30篇。 The syntheses of bile acid derivatives were reviewed with 30 references, including the applications in macromolecule material, molecular recognition and the field of medicine.
出处 《合成化学》 CAS CSCD 北大核心 2009年第2期140-145,共6页 Chinese Journal of Synthetic Chemistry
关键词 胆酸 胆酸衍生物 合成 应用 综述 bile acid bile acid derivative synthesis application review
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参考文献30

  • 1胡祥正,陆伟,刘雁红,倪丽琴.胆酸酯及其甲基丙烯酸衍生物的制备[J].合成化学,2006,14(4):360-363. 被引量:9
  • 2胡祥正,韩聪.含胆酸高分子合成应用中胆酸的化学修饰方法[J].天津科技大学学报,2004,19(3):16-19. 被引量:2
  • 3Achintya K, Bandyopadhyaya, Sangeetha N M, et al. Highly diastereoselective synthesis of the 1,1 '-binaphthol unit on a bile acid template[J]. J Org Chem,2000, 65:8239 - 8244.
  • 4Zhao Y, Zhong Z Q. Oligomeric cholates:Amphiphilic foldamers with nanometer sized hydrophilic cavities [ J ]. Am Chem Soc,2005,127 : 17894 - 17901.
  • 5Balasubramanian R, Uday M. Design and synthesis of novel chiral dendritic species derived from bile acids [ J ]. J Org Chem ,2001,66 : 3035 - 3040.
  • 6Iuliano A, Facchetti S, Barretta G U. Asymmetric induction by the cholestanic moiety on tropos species: Synthesis and stereochemical characterization of bile acid-based biphenyl phosphites [ J ]. Org Chem, 2005, 71:4943 - 4950.
  • 7Gian L P, Matteo M, Iuliano A. Synthesis of proline derivatives of bile acids and their evaluation as organocatalysts in the asymmetric direct aldol reaction [ J ]. Tetrahedron : Asymmetry ,2007,18 : 1364 - 1375.
  • 8刘兴利,赵志刚,陈淑华.新型鹅去氧胆酸分子裂缝的设计合成[J].化学研究与应用,2007,19(3):330-333. 被引量:2
  • 9Iuliano A, Pieraccini I, Felix G, et al. Synthesis of four cholic acid-based CSPs containing 2-naphthyl earbamate and 3,5-dinitrophenylearbamate moieties and their evaluation in the HPLC resolution of raeemie compounds [ J ]. Tetrahedron : Asymmetry, 2002, 13 : 1265 - 1275.
  • 10Vijay K K, Mamta C, Pavani K, et al. Bile acid - based cyclic bisbenzimidazolium receptors for anion recognition: Highly improved receptors for fluoride and chloride [ J]. J Org Chem, 2007 , 72 :10224 - 10226.

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