Recyclable indium(III) Chloride catalyzed site-selective double substitution in one pot for the synthesis of isatin N -ribonucleosides under microwave irradiation

Synthesis

Volumn , Issue 10, 2010, Pages 1613-1616

  Siddiqui, Ibadur R ^a   Singh, Archana ^a   Shamim, Shayna ^a   Srivastava, Vishal ^a   Singh, Pravin K ^a   Yadav, Sanjay ^a   Singh, Rana K P ^a  

^a UNIVERSITY OF ALLAHABAD   (India)

Author keywords

Double substitution; Indium(III) chloride; Isatin N ribonucleoside; Microwave; One pot reaction

Indexed keywords

AMBIENT TEMPERATURES; ANOMERICS; ARYL AMINES; BENZENE RING; DIETHYL OXALATES; DOUBLE SUBSTITUTION; ELECTROPHILIC SUBSTITUTIONS; HYDROXY GROUPS; ISATIN N -RIBONUCLEOSIDE; NITROGEN HETEROCYCLES; NUCLEOPHILIC SUBSTITUTIONS; ONE POT; ONE-POT REACTION; ONE-POT SYNTHESIS; QUANTITATIVE YIELDS; RIBOFURANOSE; RIBONUCLEOSIDES; SITE SELECTIVE; STARTING MATERIALS;

BENZENE; CHLORINE COMPOUNDS; ETHANOL; INDIUM; IRRADIATION; LITHIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

MICROWAVE IRRADIATION;

1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 6 CHLORO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 6 FLUORO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 6 METHOXY 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 6 NITRO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 6,7 DIMETHOXY 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 7 CHLORO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 7 FLUORO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 7 METHOXY 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; 7 NITRO 1 (BETA DEXTRO RIBOFURANOSYL) 1H INDOLE 2,3 DIONE; ALCOHOL; AMINE; DIETHYLOXALIC ACID; INDIUM CHLORIDE; ISATIN DERIVATIVE; ISATIN N RIBONUCLEOSIDE DERIVATIVE; N PHENYLRIBOSYLAMINE; OXALIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CYCLIZATION; ENVIRONMENTAL TEMPERATURE; MASS SPECTROMETRY; MICROWAVE IRRADIATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 77952027258     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218714     Document Type: Article

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