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【人名反应】Bischler-Mohlau吲哚合成反应

Bischler-Mohlau吲哚合成反应亦称Bischler吲哚合成反应。从α-卤代芳香酮和过量的苯胺环化生成3-芳基吲哚。

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反应机理

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反应实例


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参考文献


1. Möhlau, R. Ber. 1881,14, 171–175.

2. Bischler, A.; Fireman, P. Ber.1893, 26, 1346–1349. Augustus Bischler (1865-1957)

3. Sundberg, R. J. TheChemistry of Indoles; Academic Press: New York, 1970, pp 164.

4. Buu-Hoï, N. P.; Saint-Ruf,G.; Deschamps, D.; Bigot, P. J. Chem. Soc. (C) 1971,

2606–2609.

5. Houlihan, W. J., Ed.; TheChemistry of Heterocyclic Compounds, Indoles (Part 1),

Wiley: New York, 1972.(Book).

6. Bigot, P.; Saint-Ruf, G.;Buu-Hoï, N. P. J. Chem. Soc., Perkin 1 1972, 2573–2576.

7. Bancroft, K. C. C.; Ward, T.J. J. Chem. Soc., Perkin 1 1974, 1852–1858.

8. Coïc, J. P.; Saint-Ruf, G.;Brown, K. J. Heterocycl. Chem. 1978, 15, 1367–1371.

9. Henry, J. R.; Dodd, J. H. TetrahedronLett. 1998, 39, 8763–8764.

10. Pchalek, K.; Jones, A. W.;Wekking, M. M. T.; Black, D. S. C. Tetrahedron 2005, 61,

77–82.

11. Sridharan, V.; Perumal, S.;Avendaño, C.; Menéndez, J. C. Synlett 2006, 91–95.

12. Zhang, J. Bischler–MöhlauIndole Synthesis, In Name Reactions in Heterocyclic

Chemistry II; Li, J. J., Ed.; Wiley: Hoboken, NJ, 2011, pp 84-90.(Review).



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