Paper
The nitration of 1,2,3,4-tetramethyl-5,6-dinitrobenzene; X-ray crystal structure of cis-2,5,6,6-Tetramethyl-2,3,4,5-tetranitrocyclohex-3-enone
Published 1982 · M. Gray, M. P. Hartshorn, K. Richards
Australian Journal of Chemistry
Q3 SJR score
1
Citations
0
Influential Citations
Abstract
Nitration of 1,2,3,4-tetramethyl-5,6-dinitrobenzene (1) with fuming nitric acid in dichloromethane gives cis-and trans-2,5,6,6-tetramethyl-2,3,4,5-tetranitrocyclohex-3-enones (9) and (10), the structure of the cis isomer being confirmed by X-ray crystal structure analysis. The mechanism of formation of tetranitro ketones (9) and (10) is discussed.
Study Snapshot
The nitration of 1,2,3,4-tetramethyl-5,6-dinitrobenzene with fuming nitric acid in dichloromethane leads to cis- and trans-2,5,6,6-tetramethyl-2,3,4,5-tetranitrocyclohex
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Full text analysis coming soon...
References
···
···
···
···
Citations
···
···
···
···