Evolution of the pseudo-1,3-dipolar cycloaddition chemistry of SNSMF 6 (M = As, Sb) leading to 2,5-dihydroxybenzo-1,3,2-dithiazolylium and 2,7-dicarbonylnaphtha-1,3,2-dithiazolylium salts and their corresponding radicals

Chemical Communications

Volumn , Issue 18, 2005, Pages 2366-2368

  Decken, Andreas ^a   Mailman, Aaron ^a   Mattar, Saba M ^a   Passmore, Jack ^a  

^a UNIVERSITY OF NEW BRUNSWICK   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 BENZOQUINONE DERIVATIVE; 1,4 NAPHTHOQUINONE DERIVATIVE; 2,5 DIHYDROXYBENZO 1,3,2 DITHIAZOLYLIUM; 2,7 DICARBONYLNAPHTHA 1,3,2 DITHIAZOLYLIUM; ANTIMONY DERIVATIVE; ARSENIC DERIVATIVE; RADICAL; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLOADDITION; HYDROGEN BOND; REACTION ANALYSIS; ROOM TEMPERATURE; STRUCTURE ANALYSIS; SYNTHESIS; TEMPERATURE DEPENDENCE;

EID: 19844368066     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b418137a     Document Type: Article

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