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Volumn 62, Issue 14, 2006, Pages 3228-3241

Application of modified Pictet-Spengler reaction for the synthesis of thiazolo- and pyrazolo-quinolines

Author keywords

C C bond formation; Pictet Spengler reaction; Pyrazoloquinoline; Thiazoloquinoline

Indexed keywords

(4 CHLORO BENZYL) [4 (2 DIMETHYLAMINO PHENYL) THIAZOLO[5,4 C]QUINOLIN 2 YL] AMINE; (4 CHLORO BENZYL) [4 (2 NITRO PHENYL) THIAZOL 2 YL] AMINE; (4 CHLORO BENZYL) [4 (4 NITRO PHENYL) THIAZOLO[5,4 C]QUINOLIN 2 YL] AMINE; (4 CHLORO BENZYL) [4 4 TOLYL THIAZOLO[5,4 C]QUINOLIN 2 YL] AMINE; [(AMINO PHENYL) THIAZOL 2 YL] PHENYL AMINE; [4 (2 AMINO PHENYL) THIAZOL 2 YL] (4 CHLORO BENZYL) AMINE; [4 (2 AMINO PHENYL) THIAZOL 2 YL] BENZYL AMINE; [4 (2 NITRO PHENYL) THIAZOL 2 YL] PHENYL AMINE; [4 (4 BROMO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] PHENYL AMINE; [4 (4 DIMETHYLAMINO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] PHENYL AMINE; [4 (4 NITRO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] PHENYL AMINE; [4 FURAN 2 YL THIAZOLO [5,4 C]QUINOLIN 2 YL] PHENYL AMINE; ALDEHYDE; ALIPHATIC AMINE; BENZYL [4 (4 BROMO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] AMINE; BENZYL [4 (4 DIMETHYLAMINO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] AMINE; BENZYL [4 (4 NITRO PHENYL)THIAZOLO [5,4 C] QUINOLIN 2 YL] AMINE; BENZYL [4 (NITRO PHENYL) THIAZOL 2 YL] AMINE; BENZYL [4 4 TOLYL THIAZOLO[5,4 C]QUINOLIN 2 YL] AMINE; BENZYL [4 FURAN 2 YL THIAZOLO[5,4 C]QUINOLIN 2 YL] PHENYL AMINE; IMIDAZOLE; INDOLE; PHENYL [4 4 TOLYL THIAZOLO [5,4 C]QUINOLIN 2 YL] AMINE; PYRAZOLE DERIVATIVE; QUINOLINE DERIVATIVE; TETRAHYDROISOQUINOLINE DERIVATIVE; THIAZOLE DERIVATIVE; THIAZOLOQUINOLINE DERIVATIVE; TRYPTOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 33644914455     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.01.063     Document Type: Article
Times cited : (67)

References (90)
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    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press Ltd.: London
    • (a) Katritzky, A. R. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press Ltd.: London 1984, 41-110.
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    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press Ltd.: London
    • (b) Metzger, J. V. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press Ltd.: London 1984, 235-330.
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    • For illustrative examples of syntheses and pharmacological data for this structural class see: (a) P.G. Baraldi, and P.A. Borea Trends Pharmacol. Sci. 21 2000 456 459
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    • Baraldi, P.G.1    Borea, P.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.