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Volumn 63, Issue 34, 2007, Pages 8124-8134

Development of a practical synthesis of novel, pyrrole-based HMG-CoA reductase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

2 (4 FLUOROPHENYL) 1 PHENYLETHANONE; 3 CHLORO 2 (4 FLUOROPHENYL) 3 PHENYLACRYLALDEHYDE; 3 DIMETHYLAMINO 1 (4 FLUOROPHENYL) 2 PHENYLPROPENONE; 3,4 BIS(4 FLUOROPHENYL) 5 (HYDROXYMETHYL) 1 ISOPROPYL N PHENYL 1H PYRROLE 2 CARBOXAMIDE; 3,4 BIS(4 FLUOROPHENYL) 5 FORMYL 1 ISOPROPYL N PHENYL 1H PYRROLE 2 CARBOXAMIDE; 4 (4 FLUOROPHENYL) 1 ISOPROPYL 3 PHENYL 1H PYRROLE 2 CARBOXYLIC ACID ETHYL ESTER; 4 (4 FLUOROPHENYL) 5 FORMYL 1 ISOPROPYL 3 PHENYL 1H PYRROLE 2 CARBOXYLIC ACID; 4 (4 FLUOROPHENYL) 5 FORMYL 1 ISOPROPYL 3 PHENYL 1H PYRROLE 2 CARBOXYLIC ACID 4 METHOXYBENZYLAMIDE; 4 (4 FLUOROPHENYL) 5 FORMYL 1 ISOPROPYL 3 PHENYL 1H PYRROLE 2 CARBOXYLIC ACID ETHYL ESTER; 4 (4 FLUOROPHENYL) 5 HYDROXYMETHYL 1 ISOPROPYL 3 PHENYL 1H PYRROLE 2 CARBOXYLIC ACID 4 METHOXYBENZYLAMIDE; 7 [3 (4 FLUOROPHENYL) 1 ISOPROPYL 5 (4 METHOXYBENZYLCARBAMOYL) 4 PHENYL 1H PYRROL 2 YL] 3,5 DIHYDROXYHEPTANOIC ACID SODIUM SALT; 7 [3 (4 FLUOROPHENYL) 1 ISOPROPYL 5 (4 METHOXYBENZYLCARBAMOYL) 4 PHENYL 1H PYRROL 2 YL] 3,5 DIHYDROXYHEPTANOIC ACID TERTBUTYL ESTER; [3 (4 FLUOROPHENYL) 1 ISOPROPYL 5 (4 METHOXYBENZYLCARBAMOYL) 4 PHENYL 1H PYRROL 2 YLMETHYL]TRIPHENYLPHOSPHONIUM BROMIDE; [3 (4 FLUOROPHENYL) 1 ISOPROPYL 5 (PHENYLCARBAMOYL) 4 (4 FLUOROPHENYL) 1H PYRROL 2 YLMETHYL]TRIPHENYLPHOSPHONIUM BROMIDE; DIETHYL [5 (BENZYLCARBAMOYL) 3 (4 FLUOROPHENYL) 1 ISOPROPYL 4 PHENYL 1H PYRROL 2 YL]METHYLPHOSPHONATE; HEXANOIC ACID DERIVATIVE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; ISOPROPYLAMINO ACETIC ACID ETHYL ESTER; N BENZYL 2 (ISOPROPYLAMINO)ACETAMIDE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34447098447     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.06.005     Document Type: Article
Times cited : (25)

References (27)
  • 4
    • 34447102529 scopus 로고    scopus 로고
    • For reviews, see:
  • 9
    • 34447094419 scopus 로고    scopus 로고
    • For an account of the structure-activity studies and in vivo pharmacology of this series of HMG-CoA reductase inhibitors, see: Pfefferkorn, J. A.; Song, Y.; Sun, K.-L.; Miller, S. R.; Trivedi, B. K.; Choi, C.; Sorenson, R. J.; Bratton, L. D.; Unangst, P. C.; Larsen, S. D.; Poel, T.-J.; Cheng, X.-M.; Lee, C.; Erasga, N.; Auerbach, B.; Askew, V.; Dillon, L.; Hanselman, J. C.; Lin, Z.; Lu, G.; Robertson, A.; Olsen, K.; Mertz, T.; Sekerke, C.; Pavlovsky, A.; Harris, M. S.; Bainbridge, G.; Caspers, N.; Chen, H.; Eberstadt, M. Bioorg. Med. Chem. Lett., in press. doi:10.1016/j.bmcl.2007.05.097
  • 25
    • 34447104090 scopus 로고    scopus 로고
    • note
    • Karl Fisher water analysis of various phosphonium salts synthesized according to the method described in Table 3 indicated that, as expected, they contained up to 1 equiv of water; however, azeotropic drying with IPA reduced the water content to <0.5%. Attempts to remove this residual water using simply high vacuum and elevated temperature were not effective.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.