Aryne [3 + 2] cycloaddition with N-sulfonylpyridinium imides and in situ generated N-sulfonylisoquinolinium imides: A potential route to pyrido[1,2-b]indazoles and indazolo[3,2-a]isoquinolines

Organic and Biomolecular Chemistry

Volumn 10, Issue 9, 2012, Pages 1922-1930

  Zhao, Jingjing ^a   Li, Pan ^a   Wu, Chunrui ^a   Chen, Hongli ^a   Ai, Wenying ^a   Sun, Renhong ^a   Ren, Hailong ^a   Larock, Richard C ^b   Shi, Feng ^a  

^a HENAN UNIVERSITY   (China)

^b IOWA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-CANCER AGENTS; AROMATICITIES; CYCLOADDITION PROCESS; ELECTROPHILIC CYCLIZATION; IN-SITU; ISOQUINOLINES; PYRIDINE RINGS; PYRIDINIUM; SULFONYL GROUPS;

CYCLIZATION;

AMINES;

IMIDE; INDAZOLE DERIVATIVE; ISOQUINOLINE DERIVATIVE; NITROGEN; PHENAZOPYRIDINE; SULFUR DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION;

CYCLIZATION; IMIDES; INDAZOLES; ISOQUINOLINES; MOLECULAR STRUCTURE; NITROGEN; PHENAZOPYRIDINE; SULFUR COMPOUNDS;

EID: 84863116121     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob06611d     Document Type: Article

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