An approach to the synthesis of 2-Acylchromeno[3,4- c ]pyrrol-4(2 H)-one derivatives via a sequential three-component reaction

Synlett

Volumn 24, Issue 16, 2013, Pages 2124-2126

  Alizadeh, Abdolali ^a   Ghanbaripour, Rashid ^a   Zhu, Long Guan ^b  

^a TARBIAT MODARES UNIVERSITY   (Iran)

^b ZHEJIANG UNIVERSITY   (China)

Author keywords

2 acylchromeno 34 c pyrrol 4(2 H) one; 13 acyl shift; p toluenesulfonylmethyl isocyanide; salicylaldehyde

Indexed keywords

2 ACYLCHROMENO[3,4 C]PYRROL 4(2H)ONE DERIVATIVE; 2 ALKYLCARBOXYLATECHROMENO[3,4 C]PYRROL 4(2H)ONE DERIVATIVE; 2 HYDROXYNAPHTHALENE 1 CARBALDEHYDE; 3 ACETYLCOUMARIN DERIVATIVE; 3,5 DICHLOROSALICYLALDEHYDE; 4 METHOXYSALICYLALDEHYDE; 4 TOLUENESULFONYLMETHYLISOCYANIDE; 5 CHLOROSALICYLALDEHYDE; 5 METHOXYSALICYLALDEHYDE; 5 NITROSALICYLALDEHYDE; ALDEHYDE DERIVATIVE; BETA KETO ESTER DERIVATIVE; CHEMICAL COMPOUND; COUMARIN DERIVATIVE; ESTER DERIVATIVE; ORTHO VANILLIN; PIPERIDINE; PYRROLE DERIVATIVE; SALICYLALDEHYDE; TRIETHYLAMINE; UNCLASSIFIED DRUG;

ABSORPTION; AROMATIZATION; ARTICLE; BAYLIS HILLMAN REACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONJUGATION; CRYSTAL STRUCTURE; CYCLIZATION; CYCLOADDITION; DEACYLATION; ELECTROPHILICITY; KNOEVENAGEL CONDENSATION; MASS SPECTROMETRY; MICHAEL ADDITION; SEQUENTIAL THREE COMPONENT REACTION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 84883193825     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0033-1339521     Document Type: Article

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