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Volumn 2004, Issue 5, 2004, Pages 181-195
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A general, versatile synthesis of 2H-pyrrolo[3,4-c]quinolines via tosylmethylisocyanide reaction
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Author keywords
Pyrroloquinolines; Synthesis; TosMIC
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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;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
REDUCTION;
SYNTHESIS;
TECHNIQUE;
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EID: 2942694389
PISSN: 14246376
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (12)
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References (15)
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