
TY  - JOUR
A1  - Hartshorn, MP 
A1  - Robinson, WT 
A1  - Wright, GJ 
A1  - Cheng, LY 
T1  - <sup>15</sup>N-Labeling Study of the Rearrangement of r-2,4-Dichloro-t-6-hydroxy-3,6-dimethyl-2,T-5-dinitrocyclohex-3-enone to 4-Chloro-c-6-hydroxy-3,6-dimethyl-r-5-nitro-cyclohex-3-ene-1,2-dione
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1989
VL  - 42
IS  - 9
SP  - 1569
EP  - 1578
KW  - 
UR  - https://doi.org/10.1071/CH9891569 
N2  - Reaction of hydroxy dinitro ketone (15) in solution gives the &#945;-diketone (16). This reaction has been shown, by means of 15N n.m.r. spectroscopy, to occur via C2-epimeric nitro nitrites (19) and (20). X-Ray crystal analyses are reported for hydroxy dinitro ketone (15) and &#945;-diketone (16). 
ER  -

