Bergman cyclization of acyclic amino acid derived enediynes leads to the formation of 2,3-dihydrobenzo[ f ]isoindoles

Journal of Organic Chemistry

Volumn 75, Issue 18, 2010, Pages 6219-6228

  Gredičak, Matija ^a   Matanović, Ivana ^a   Zimmermann, Boris ^a   Jerić, Ivanka ^a  

^a RUDER BO KOVI INSTITUTE   (Croatia)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE FUNCTIONALITY; BERGMAN CYCLIZATION; COMPUTATIONAL DATA; DIRADICALS; ENEDIYNES; EXTERNAL DONOR; H-ATOM ABSTRACTION; ISOINDOLES; RECOGNITION ELEMENT; SIDE CHAINS; THERMALLY INDUCED;

ACETYLENE; AMINO ACIDS; BENZENE; ORGANIC ACIDS; PEPTIDES;

CYCLIZATION;

2,3 DIHYDROBENZO[F]ISOINDOLE DERIVATIVE; ENEDIYNE; ISOINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

AROMATIZATION; ARTICLE; BERGMAN CYCLIZATION; CYCLIZATION; ELIMINATION REACTION; HEATING; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION;

AMINO ACIDS; CYCLIZATION; ENEDIYNES; ISOINDOLES; MOLECULAR DYNAMICS SIMULATION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 77956512884     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101302n     Document Type: Article

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