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丁酸氯维地平(Cleviprex) 被引量:5

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作者 郑伟 胡春
机构地区 沈阳药科大学
出处 《中国药物化学杂志》 CAS CSCD 2009年第1期79-79,共1页 Chinese Journal of Medicinal Chemistry
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参考文献6

  • 1USFDA. FDAapprovalletter [ EB/QL]. [ 2008 - 08 - 01 ].http://www, fda. gov/cder/foi/appletter/2008/022156s0001tr. pdf.
  • 2SUH J J, HONG Y H. Synthesis of 1,4-dihydropyridine carboxylic acids ( II ) [ J ]. Yakhak Hoechi, 1989, 33 ( 4 ) : 219 -225.
  • 3SORBERA L A, CASTANER L Clevidipine: treatment of hypertension calcium channel blocker [ J ]. Drugs Fut, 2004,29 (2) :105 -111.
  • 4MATTSON A ,SVENSSON C,THORNBLOM K,et al. Manufacture of clevidipine from 4- ( 2', 3'-dichlorophenyl ) -1,4-di- hydro-5-methoxycarbonyl -2,6-dimethyl-3- pyridinecarboxylic acid: WO,2000/031035 [ P ]. 2000 - 06 - 02.
  • 5WHEELER T N,KENAKIN T P. Preparation of 4-aryl-1,4-dihydropyridine -3,5-dicarboxylates as vasodilators: US, 1992/ 5100892 [ P]. 1992 - 05 - 31.
  • 6VARON J. Treatment of acute severe hypertension: current and newer agents[ J]. Drugs,2008,68 (3) :283 - 297.

同被引文献52

  • 1张婧,纪宪勇,孙翔,王杰.氯维地平的合成[J].中国医药工业杂志,2011,42(7):484-486. 被引量:4
  • 2徐云根,华维一.尼莫地平的合成改进[J].中国医药工业杂志,2005,36(1):8-9. 被引量:6
  • 3王玉民,曹晓群,朱焰,张昌军,庞现红.特戊酸氯甲酯合成新工艺的研究[J].泰山医学院学报,2005,26(4):346-347. 被引量:2
  • 4辜正一,朱源.西尼地平的合成工艺改进[J].中国现代应用药学,2006,23(3):204-205. 被引量:4
  • 5US FDA, FDA approval letter [EB/OL]. [2008-08-10]. http://www.fda.gov/cder/foi/appletter/2008/022156s0001tr. pdf.
  • 6Varon J. Treatment of acute severe hypertension: current and newer agents [J]. Drugs, 2008, 68 (3) : 283-297.
  • 7Andersson KH, Nordlander M, Westerlund RC. Preparation of short-acting 2,6-dimethyl-4-phenyl-l,4-dihydropyridine- 3,5-dicarboxylate calcium antagonist antihypertensives: WO, 9512578 [P]. 1995-05-11. (CA 1995, 123: 313768).
  • 8Kosugi Y, Hori M, Nagasaka T. Synthesis of optically pure 1,4-dihydropyridine derivatives by means of diastereoisomeric separation of the hantzsch intermediates bearing (R)-l-phenylethylamino group [J]. Heterocycles, 1994, 39 (2): 591-602.
  • 9Mattson A, Svensson C, Thornblom K, et al. Manufacture of clevidipine from 4- (2,3-dichlorophenyl) -1,4-dihydro-5- methoxycarbonyl-2,6-dimethyl-3-pyridinecarboxylic acid: WO, 2000031035 [P]. 2000-06-02. (CA2000, 133: 6161).
  • 10Che D, Guntoori BR, Murthy KKS. Process to prepare 1,4-dihydropyridine intermediates and derivatives thereof: US, 20040204604 [P]. 2004-10-14.

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