Synthesis of quinolines via friedländer reaction in water and under catalyst-free conditions

Synthesis

Volumn 44, Issue 3, 2012, Pages 389-392

  Shen, Qiang ^a   Wang, Limin ^a   Yu, Jianjun ^a   Liu, Mingtao ^a   Qiu, Jun ^a   Fang, Lei ^a   Guo, Fenglou ^a   Tang, Jun ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

catalyst free; Friedl nder reaction; ketones; quinolines; water

Indexed keywords

CATALYST-FREE; MALONONITRILES; QUINOLINES;

CATALYSTS; KETONES; ORGANIC COMPOUNDS; WATER;

SYNTHESIS (CHEMICAL);

1,3 DIKETONE; 1,3 INDANDIONE DERIVATIVE; 2 CYANOACETOPHENONE; 5,5' DIMETHYLCYCLOHEXA 1,3 DIONE; ACETOACETIC ACID ETHYL ESTER; ACETOACETIC ACID METHYL ESTER; ACETYLACETONE; ALCOHOL; AMINOBENZALDEHYDE; BARBITURIC ACID; CYCLOHEXA 1,3 DIONE; ETHYL 2 (3,4 DIHYDRO 2H PYRAN 6 YL)QUINOLINE 3 CARBOXYLIC ACID; ETHYL 3 (3,4 DIHYDRO 2H PYRAN 6 YL) 3 OXOPROPANOIC ACID; MALONONITRILE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG SYNTHESIS; FRIEDLANDER REACTION; HYDROGEN BOND; KNOEVENAGEL CONDENSATION; NUCLEOPHILICITY; SOLUBILITY; SUBSTITUTION REACTION; TEMPERATURE SENSITIVITY;

EID: 84856228222     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289657     Document Type: Article

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