An o-iminothioquinone: Its cycloaddition to produce an indologlycoside and its self-dimerization to form a dithio-diazocycloctane, the structure assignment of which is based on the DFT prediction of its IR spectrum

Journal of Organic Chemistry

Volumn 68, Issue 20, 2003, Pages 7907-7910

  Diep, Vinh ^a,b   Dannenberg, J J ^a,b   Franck, Richard W ^a,b  

^a CITY UNIVERSITY OF NEW YORK   (United States)

^b CITY UNIVERSITY OF NEW YORK   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITION;

DIMERS; INFRARED SPECTROSCOPY;

AROMATIC COMPOUNDS;

2 IMINOTHIOQUINONE; GLYCOSIDE; INDOLOQUINOLINE DERIVATIVE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; DIMERIZATION; INFRARED SPECTROSCOPY; PREDICTION; STRUCTURE ANALYSIS; SYNTHESIS; THEORY;

CYCLIZATION; DIMERIZATION; GLYCOSIDES; GLYCOSYLATION; IMINES; INDOLES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; QUINONES; SPECTROPHOTOMETRY, INFRARED;

EID: 0141542721     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034800e     Document Type: Article

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