Dess-martin periodinane mediated intramolecular cyclization of phenolic azomethines: A solution-phase strategy toward benzoxazoles and benzothiazoles

Synthesis

Volumn , Issue 3, 2010, Pages 398-402

  Bose, D Subhas ^a   Idrees, Mohd ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Azomethines; Benzothiazoles; Benzoxazoles; Dess Martin periodinane; Intramolecular cyclization; Solution phase strategy

Indexed keywords

AMBERLYST; AMBIENT TEMPERATURES; AZOMETHINES; BENZOTHIAZOLES; DESS-MARTIN PERIODINANE; HYPERVALENT IODINE; INTRAMOLECULAR CYCLIZATIONS; REACTION MIXTURE;

IODINE; PHENOLS; RESINS; SYNTHESIS (CHEMICAL);

CYCLIZATION;

2 AMINOPHENOL; 2 AMINOTHIOPHENOL; AMBERLYST A 26 THIOSULFATE RESIN; BENZOTHIAZOLE DERIVATIVE; BENZOXAZOLE DERIVATIVE; DESS MARTIN PERIODINANE; DICHLOROMETHANE; DIISOPROPYLAMINOMETHYL RESIN; IODINE; IODINE DERIVATIVE; ION EXCHANGE RESIN; MONTMORILLONITE; PHENOL DERIVATIVE; REAGENT; SCHIFF BASE; THIOSULFATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; COMBINATORIAL CHEMISTRY; CYCLIZATION; ENVIRONMENTAL TEMPERATURE; INTRAMOLECULAR CYCLIZATION; PURIFICATION; SOLUTION PHASE COMBINATORIAL SYNTHESIS; SYNTHESIS;

EID: 75849120845     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1217136     Document Type: Article

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