Recent developments on ultrasound-assisted one-pot multicomponent synthesis of biologically relevant heterocycles

Ultrasonics Sonochemistry

Volumn 35, Issue , 2017, Pages 15-35

  Banerjee, Bubun ^a  

^a Indus International University   (India)

Author keywords

Biologically active heterocycles; Multi component reactions; Sonochemistry; Sustainable synthesis; Ultrasonic irradiation

Indexed keywords

REACTION RATES; SONOCHEMISTRY; ULTRASONIC APPLICATIONS;

GREEN AND SUSTAINABLE CHEMISTRIES; HETEROCYCLES; MULTI-COMPONENT REACTIONS; MULTICOMPONENT REACTIONS (MCRS); MULTICOMPONENT SYNTHESIS; NATURALLY OCCURRING; PRODUCT SELECTIVITIES; ULTRASOUND IRRADIATION;

SYNTHESIS (CHEMICAL);

1,4 DIHYDROPYRIDINE DERIVATIVE; 1,8 DIOXO DECAHYDROACRIDINE DERIVATIVE; 2 AMINO 4H CHROMENE DERIVATIVE; 2,4,5 TRIARYLIMIDAZOLE DERIVATIVE; 3' AMINOSPIROSPIRO[INDOLINE 3,1' PYRAZOLO[1,2 B]PHTHALAZINE DERIVATIVE; 4 AMINO 5 CARBOXAMIDO 1,2,3 TRIAZOLE DERIVATIVE; 4 OXO 2 THIOXOHEXAHYDROPYRIMIDINE DERIVATIVE; 8 ARYL 7,8 DIHYDRO[1,3]DIOXOLO[4,5 G]QUINOLIN 6(5H) ONE; BENZIMIDAZO[2,1 B]QUINAZOLIN 1(1H) ONE DERIVATIVE; BENZO[F]CHROMEN INDOLE DERIVATIVE; BIQUINOLINE DERIVATIVE; DISPIROPYRROLIZIDINE DERIVATIVE; HETEROCYCLIC COMPOUND; IMIDAZO[4,5 B]INDOLE DERIVATIVE; INDENONAPHTHOPYRAN DERIVATIVE; PYRAZOLO[3,4 B]PYRIDINE DERIVATIVE; PYRIDAZINE DERIVATIVE; PYRIDO[2,3 D:6,5 D]DIPYRIMIDINE DERIVATIVE; PYRIDO[2,3 D]PYRIMIDINE DERIVATIVE; PYRIMIDINE 5 CARBOXYLIC ACID DERIVATIVE; PYRROLE DERIVATIVE; PYRROLIDINE 2 SPIRO 3' OXINDOLE DERIVATIVE; SPIROPYRROLIDINE DERIVATIVE; SPIROPYRROLIZIDINE DERIVATIVE; SPIRO[INDOLINE 3,4' PYRAZOLO[3,4 B]PYRIDINE] 2,6'(1'H) DIONE DERIVATIVE; TETRAHYDROBENZO[A]XANTHEN 11 ONE DERIVATIVE; TETRAHYDROPYRIDINE 3,5 DICARBONITRILE DERIVATIVE; TRIAZOLO[4,3 A]PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

BIOLOGICAL ACTIVITY; CHEMICAL REACTION; DRUG SYNTHESIS; MULTICOMPONENT REACTION; ONE POT SYNTHESIS; PRIORITY JOURNAL; REVIEW; SUBSTITUTION REACTION; ULTRASOUND;

EID: 85000936630     PISSN: 13504177     EISSN: 18732828     Source Type: Journal    
DOI: 10.1016/j.ultsonch.2016.10.010     Document Type: Review

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