期刊文献+

高效液相色谱法测定1-三甲基硅基-1-炔-3-癸醇对映体纯度

Determination of Enantiomeric Purity of 1-Trimethylsilyl-1-decyn-3-ol by Chiral HPLC
下载PDF
导出
摘要 以苯甲酰氯试剂衍生1-三甲基硅基-1-炔-3-癸醇,得到具有强紫外吸收的1-三甲基硅基-1-癸炔-3-苯甲酸酯.考察流动相中不同醇调节剂、乙醇含量和柱温对外消旋1-三甲基硅基-1-癸炔-3-苯甲酸酯对映体在Chiralcel OD-H手性柱上色谱分离的影响,建立测定1-三甲基硅基-1-炔-3-癸醇对映体纯度的色谱分析方法.结果表明:以正己烷-乙醇(99.950.05,体积比)为流动相,检测波长为228nm,外消旋苯甲酰氯衍生对映体在Chiralcel OD-H柱上得到很好的分离,保留时间分别为6.94min和8.11min,分离因子和分辨率分别为1.41和3.75.本法灵敏度高,方法简便,适合于手性1-三甲基硅基-1-炔-3-癸醇样品的对映体纯度分析. A simple and accurate method for determination of the enantiomeric purity of 1-trimethylsilyl-1-decyn-3-ol by chiral hlgh-performance liquid chromatography was established. The 1-decyn-3-ol enantiomers were derivatized with benzoyl chloride by esterification to the benzoates,which could be detected sensitively by an UV monitor. The racemic 3-benzoyloxy -1-trimethylsilyl-l-decyne was completely resolved on Chiralcel OD-H column using n-hexane-ethanol (99.95 : 0.05, by vol. ) as mobile phase in 9 minutes,the values of a and Rs were 1.41 and 3.75 respectively. The effects of different alcohol modifiers and ethanol percentage in mobile phase,as well as column temperature on chiral separation of the benzoate derivatives were discussed. Precision,linearity and limit of detection of the chromatographic method were also evaluated.
出处 《厦门大学学报(自然科学版)》 CAS CSCD 北大核心 2008年第4期537-540,共4页 Journal of Xiamen University:Natural Science
基金 福建省自然科学基金(C0510001) 国家基础科学人才培养基金(J0630429)资助
关键词 高效液相色谱法 对映体拆分 1-三甲基硅基-1-炔-3-癸醇 紫外衍生 HPLC enantiomeric resolution 1-trimethylsilyl- 1-decyn-3-ol ultraviolet derivatization
  • 相关文献

参考文献15

  • 1何绮雯,麻生明.光学活性炔丙醇的合成[J].有机化学,2002,22(6):375-387. 被引量:2
  • 2Hirayama L C, Dunham K K, Singaram B. Asymmetric indium-mediated synthesis of homopropargylic alcohols[J]. Tetrahedron Letters, 2006,47 : 5173- 5176. 被引量:1
  • 3Chen Z C, Hui X P, Yin C, et al. Highly enantioselective addition of phenylacetylene to aldehydes catalyzed by titanium(IV) complexes of fl-hydroxy amides[J]. J Molecular Catalysis A: Chemical, 2007,269 : 179-182. 被引量:1
  • 4Nakajima M,Saito M, Hashimoto S. Selective synthesis of optically active allenic and homopropargylic alcohols from propargyl chloride [ J ]. Tetrahedron: Asymmetry, 2002, 13:2449-2452. 被引量:1
  • 5Gao G, Moore D, Xie R G, et al. Highly enantioselective phenylacetylene additions to both aliphatic and aromatic aldehydes[J]. Org Lett,2002,4(23) :4143-4146. 被引量:1
  • 6Helal C J, Magriotis P A,Corey E J. Direct catalytic enantioselective reduction of achiral α,β-ynones. Strong remote steric effects across the C-C triple bond[J]. J Am Chem Soc, 1996,118 : 10938-10939. 被引量:1
  • 7Chun J, Byun H S,Bittman R. Preparation of chiral propargylic alcohols from α,β-unsaturated esters[J]. Tetrahedron Letters, 2002,43 : 8043-8045. 被引量:1
  • 8Matsumura K, Hashiguchi S,Ikariya T,et al. Asymmetric transfer hydrogenation of α,β-acetylenic ketones[J]. J Am Chem Soc, 1997,119 :8738 - 8739. 被引量:1
  • 9Raminelli C, Comsseto J V, Andrade L H, et al. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase(Novozyme 435) [J]. Tetrahedron: Asymmetry,2004,15:3117-3122. 被引量:1
  • 10Jang J H , Kanoh K, Adachi K, et al. Awajanomycin, a cytotoxic γ-lactone-δ-lactam metabolite from marine-derived Acremonium sp. AWA16-1[J]. J Nat Prod, 2006, 69(9):1358-1360. 被引量:1

二级参考文献70

  • 1[1]Koob R, Rudolph C, Veith H J. The absolute configuration of 3-methylpyrrolidine alkaloids from poison glands of ants leptothoracini (Myrmicinae) [J]. Helv. Chim. Acta, 1997, 80: 267―272. 被引量:1
  • 2[2]Veith H J, Collas M, Zimmer R. Simple synthesis of both enantiomers of 3-methyl-N-(3-methylbutyl)pyrrolidine [J]. Liebigs Ann./Recueil, 1997, 2: 391―394. 被引量:1
  • 3[3]Lin J, Chan W H, Lee A W M, et al. Asymmetric synthesis of 1,3-and 1,3,4-substituted pyrrolidines [J]. Tetrahedron Lett., 2000, 41: 2 949―2 951. 被引量:1
  • 4[4]Zheng X, Huang P Q, Ruan Y P, et al. A new approach for asymmetric synthesis of (R)-3-methylpyrolidine alkaloids form (S)-malic acid [J]. Nat. Prod. Lett., 2002, 16 (1): 53―56. 被引量:1
  • 5[5]Zheng X, Huang P Q, Ruan Y P, et al. A new asymmetric synthesis of (R)-3-methylpyrrolidine alkaloids starting from (S)-malic acid [J]. Heterocycles, 2001, 55: 1 505―1 518. 被引量:1
  • 6[6]Rossi R, Diversi P, Ingrosso G. Relation between the optical rotatory power and the optical purity of (R) (+)-methylsuccinic acid [J]. Gazz. Chim. Ital., 1968, 98: 1 391―1 399. 被引量:1
  • 7[7]Ringdahl B, Dahlbom R. Acetylene compounds of potential pharmacological value. XXXVII, stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group [J]. Acta Pharm. Suec., 1978, 15: 255―263. 被引量:1
  • 8[8]Leuenberger H G W, Boguth W, Barner R, et al. Total synthesis of natural α-Tocopherol [J]. Helv. Chim. Acta ,1979, 62: 455―463. 被引量:1
  • 9[9]Feringa B L, Lange B de, Jong J C de J. Synthesis of enantiomerically pure γ-(methyloxy)butenolides and (R)-and (S)-2-methyl-1,4-butanediol [J]. J. Org. Chem., 1989, 54: 2 471―2 475. 被引量:1
  • 10Kazuei Igarashi, Keiko Kashiwagi. Polyamines: Mysterious modulators of cellular functions [ J ]. Biochem Biophys Res Commun, 2000, 271(3): 559-564. 被引量:1

共引文献13

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