Forced brominative deoxygenation improves the one-step conversion of a ketone to an alkenyl bromide

Advanced Synthesis and Catalysis

Volumn 339, Issue 2, 1997, Pages 184-186

  Behringer, Claudia ^a   Knorr, Rudolf ^a  

^a UNIVERSITY OF MUNICH   (Germany)

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[No Author keywords available]

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EID: 2842612864     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Part 17: Ref. [15]
2. U. von Roman, J. Ruhdorfer, R. Knorr, Synthesis 1993, 985
3. For some pertinent citations see ref. [2] and also U. von Roman, R. Knorr, C. Behringer, J. Ruhdorfer, J. Prakt. Chem. 336 (1994) 260
4. R. C. Fuson, S. L. Scott, E. C. Horning, C. H. McKeever, J. Am. Chem. Soc. 64 (1940) 2091
5. P. de Jong, Recl. Trav. Chim. Pays-Bas 61 (1942) 539
6. Ref. [2] provides detailed illustrations of the normal and alternative procedures, limitations, side products, and re-formation of ketones.
7. F. Kröhnke, H. Timmler, Chem. Ber. 69 (1936) 614
8. R. Knorr, Chem. Ber. 113 (1980) 2441
9. U. Vögeli, W. von Philipsborn, Org. Magn. Reson. 7 (1975) 617
10. E. J. Panek, B. L. Neff, H. Chu, M. G. Panek, J. Am. Chem. Soc. 97 (1975) 3996
11. Adapted from the procedure used by R. Knorr, J. Ruhdorfer, P. Böhrer, H. Bronberger, E. Räpple, Liebigs Ann. Chem. 1994, 433
12. K. W. F. Kohlrausch, A. Pongratz, Monatsh. Chem. 64 (1934) 361, on p. 372
13. E.g., see L. Friedman, H. Shechter, J. Org. Chem. 26 (1961) 2522
14. Compound 12f in ref. [2].
15. R. Knorr, J. Ruhdorfer, J. Mehlstäubl, P. Böhrer, D. S. Stephenson, Chem. Ber. 126 (1993) 747