Nucleophilic substitution in organomercury halides by a free radical chain process
作者:Glen A. Russel、James Hershberger、Karen Owens
DOI:10.1016/s0022-328x(00)86809-6
日期:1982.2
Nucleophilic substitution in organomercury halides by a free-radical chain process (SRN1)
作者:Glen A. Russell、J. Hershberger、Karen Owens
DOI:10.1021/ja00499a059
日期:1979.2
KATRITZKY A. R.; VILLE G. DE; PATEL R. C., TETRAHEDRON, 1981, 37, SUPPL. NO 9, 25-30
作者:KATRITZKY A. R.、 VILLE G. DE、 PATEL R. C.
DOI:——
日期:——
KATRITZKY, A. R.;KASHMIRI, M. AKRAM;WITTMANN, D. K., TETRAHEDRON, 1984, 40, N 9, 1501-1510
作者:KATRITZKY, A. R.、KASHMIRI, M. AKRAM、WITTMANN, D. K.
DOI:——
日期:——
The c-alkylation of nitroalkame anions by l-substituted-2--butyl-4-phenyl- and -2,4-diphenyl-5,6-dihydrobenzo(ulbarh]quinolinium cations
作者:Alan R. Katritzky、M. Akram Kashmiri、Dieter K. Wittmann
DOI:10.1016/s0040-4020(01)91797-1
日期:1984.1
- The N-substituents are transferred from the title cations to the C-atom of nitroalkane anions in highyield at 25-80°C in DMSO solution. The title cations are readily available from the appropriate pyrylium cations and primary amines of types RCH2,NH2, and RR'CHNH2, allowing a general 2-step method for the preparation of higher nitro- alkanes. Spectral properties of a variety of nitroalkanes are