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Volumn 2004, Issue 5, 2004, Pages 181-195

A general, versatile synthesis of 2H-pyrrolo[3,4-c]quinolines via tosylmethylisocyanide reaction

Author keywords

Pyrroloquinolines; Synthesis; TosMIC

Indexed keywords

1 METHYL 2H PYRROLO[3,4 C]QUINOLIN 4(5H) ONE; 2 PHENYL 2H PYRROLO[3,4 C]QUINOLIN 4(5H) ONE; 2H PYRROLO[3,4 C]QUINOLIN 4(5H)ONE; 2H PYRROLO[3,4 C]QUINOLINE; 2H PYRROLO[3,4 C]QUINOLINE DERIVATIVE; 3 METHYL 2H PYRROLO[3,4 C]QUINOLIN 4(5H) ONE; 4 (2 NITROPHENYL) 1H PYRROLE 3 CARBOXYLIC ACID ETHYL ESTER; 4 (5 CHLORO 2 NITROPHENYL) 5 METHYL 1H PYRROLE 3 CARBOXYLIC ACID ETHYL ESTER; 8 CHLORO 2 METHYL 2H PYRROLO[3,4 C]QUINOLIN 4(5H) ONE; 8 CHLORO 2 METHYL 2H PYRROLO[3,4 C]QUINOLINE; 8 CHLORO 2 METHYL 4 (4 METHYLPIPERAZIN 1 YL) 2H PYRROLO[3,4 C]QUINOLINE; 8 CHLORO 2,3 DIMETHYL 2H PYRROLO[3,4 C]QUINOLINE; 8 CHLORO 2H PYRROLO[3,4 C]QUINOLIN 4(5H) ONE; 8 CHLORO 4 (4 METHYLPIPERAZIN 1 YL) 2H PYRROLO[3,4 C]QUINOLINE; 8 CHLORO 4 METHOXY 2 METHYL 2H PYRROLO[3,4 C]QUINOLINE; 8 CHLORO 4 METHOXY 2H PYRROLO[3,4 C]QUINOLINE; ESTER DERIVATIVE; ETHYL 2 NITROCINNAMATE; QUINOLINE DERIVATIVE; TOLUENE 4 SULFONYLMETHYLISOCYANIDE; TOLUENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 2942694389     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (15)
  • 1
    • 0001202193 scopus 로고
    • Condensed pyrazines
    • Chap. XXXV, and references cited therein, John. Wiley & Sons Ed., UK
    • Cheesman, G. W. H.; Cookson, R. F. Condensed Pyrazines,Heterocyclic Compounds, Vol. 35, Chap. XXXV, pag. 598-653, and references cited therein, John. Wiley & Sons Ed., UK, 1979.
    • (1979) Heterocyclic Compounds , vol.35 , pp. 598-653
    • Cheesman, G.W.H.1    Cookson, R.F.2
  • 3
    • 25044432092 scopus 로고
    • Japan, 71 11,021 (Cl. C07d, A61k), 20 Mar 1971, Appl. 14 Dec 1966
    • Umio S.; Kariyone K.; Nakamura H.; Japan, 71 11,021 (Cl. C07d, A61k), 20 Mar 1971, Appl. 14 Dec 1966 [Chem. Abs. 1971, 75, 49056k].
    • (1971) Chem. Abs. , vol.75
    • Umio, S.1    Kariyone, K.2    Nakamura, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.