Convenient amination of weakly activated thiophenes, furans and selenophenes in aqueous media
摘要:
We describe herein a new amination procedure of weakly activated heterocyclic bromo derivatives in aqueous media. The base catalysed mechanism of this reaction is also confirmed. Moreover, the application of this strategy to the preparation of amino furans and selenophenes is outlined. (C) 1999 Elsevier Science Ltd. All rights reserved.
Mono- and dimethine dyes from 2-dimethylamino-5-formylfurans,-thiophenes, and -selenophenes
作者:F. A. Mikhailenko、L. I. Shevchuk、I. T. Rozhdestvenskaya
DOI:10.1007/bf00470067
日期:1975.3
Mikhailenko,F.A. et al., Journal of Organic Chemistry USSR (English Translation), 1972, vol. 8, p. 2014 - 2018
作者:Mikhailenko,F.A. et al.
DOI:——
日期:——
Shulezhko,A.A., Soviet progress in chemistry, 1972, vol. 38, # 1, p. 69 - 72
作者:Shulezhko,A.A.
DOI:——
日期:——
Convenient amination of weakly activated thiophenes, furans and selenophenes in aqueous media
作者:Damien Prim、Gilbert Kirsch
DOI:10.1016/s0040-4020(99)00318-x
日期:1999.5
We describe herein a new amination procedure of weakly activated heterocyclic bromo derivatives in aqueous media. The base catalysed mechanism of this reaction is also confirmed. Moreover, the application of this strategy to the preparation of amino furans and selenophenes is outlined. (C) 1999 Elsevier Science Ltd. All rights reserved.