N-15-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
N-15-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
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DOI：
10.1071/ch9891569
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发表时间：
1989-01-01
影响因子：
1.1
通讯作者：
CHENG, LY
中科院分区：
文献类型：
--
作者：
HARTSHORN, MP;ROBINSON, WT;CHENG, LY
Reaction of hydroxy dinitro ketone (15) in solution gives the α-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 α-diketone (16).
