Document Detail


Stability and ring-shift tautomerization of cyclic anhydrides of benzenehexasulfonic acid.
MedLine Citation:
PMID:  20557074     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Upon heating in a dry atmosphere, benzenehexasulfonic acid forms three cyclic anhydrides. Mono- and dianhydride do not hydrolyze readily due their flatter structures compared to the hydrolysis products. The trianhydride appears more to be reactive toward hydrolysis. In solutions, the mono- and dianhydride undergo ring-shift tautomerization, which is in the latter case shifted toward the para isomer.
Authors:
Evgeny M Garanin; Yuriy V Tolmachev; Robert R Hoover; Sonya Adas; Scott D Bunge; Mahinda Gangoda; Anatoly K Khitrin; Stephan M Woods; Andrey Malkovskiy; Nulifer Solak; Chrys Wesdemiotis
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  The Journal of organic chemistry     Volume:  75     ISSN:  1520-6904     ISO Abbreviation:  J. Org. Chem.     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-07-09     Completed Date:  2010-12-14     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985193R     Medline TA:  J Org Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4860-3     Citation Subset:  -    
Affiliation:
Kent State University, Kent, Ohio 44240, USA.
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