Substitution alters the mode of molecular iodine-mediated intramolecular cyclization: Syntheses of benzoxepine and benzo-2 H-pyran derivatives

Synthesis

Volumn , Issue 20, 2011, Pages 3287-3296

  Majumdar, Krishna C ^a,c   Ansary, Inul ^a   Sinha, Biswajit ^a   Roy, Brindaban ^a   Sridhar, Balasubramanian ^b  

^a UNIVERSITY OF KALYANI   (India)

^b INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^c TEZPUR UNIVERSITY   (India)

Author keywords

benzo 2 H pyrans; benzoxepine; intramolecular cyclization; iodine

Indexed keywords

BENZO-2 H -PYRANS; BENZOXEPINE; ELECTROPHILIC CYCLIZATION; INTRAMOLECULAR CYCLIZATIONS; IODOCYCLIZATION; PROPARGYL; SIMPLE SUBSTITUTION;

IODINE;

CYCLIZATION;

BENZO 2H PYRAN DERIVATIVE; BENZOXEPIN DERIVATIVE; IODINE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CYCLIZATION; ELECTROPHILICITY; INTRAMOLECULAR CYCLIZATION; SYNTHESIS;

EID: 80053899731     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260196     Document Type: Article

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