The Witkop-Winterfeldt oxidation converts tetrahydropyridoindoles into pyrroloquinolones and cinnolines by an unprecedented scaffold rearrangement

Tetrahedron

Volumn 67, Issue 5, 2011, Pages 965-970

  Mentel, Matthias ^a   Peters, Martin ^a,b   Albering, Jörg ^c   Breinbauer, Rolf ^a,b  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b GRAZ UNIVERSITY OF TECHNOLOGY   (Austria)

^c GRAZ UNIVERSITY OF TECHNOLOGY   (Austria)

Author keywords

Cinnolines; Indole rearrangement; Ozonolysis; Suzuki coupling; Witkop Winterfeldt oxidation

Indexed keywords

CINNOLINE DERIVATIVE; INDOLE DERIVATIVE; OZONE; PHENYLHYDRAZINE DERIVATIVE; PIPERIDONE DERIVATIVE; PYRIDINE DERIVATIVE; PYRROLINE DERIVATIVE; QUINOLONE DERIVATIVE; TETRAHYDROPYRIDOINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; OXIDATION; OZONOLYSIS; PRIORITY JOURNAL; REACTION ANALYSIS; SUZUKI REACTION; WITKOP WINTERFELDT OXIDATION;

EID: 78651376691     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.11.110     Document Type: Article

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