Reductive Decyanation of Annulated Aminocyclopropane-endo-carbonitriles - A Way to Annulated Cyclopropane-exo-amines

Advanced Synthesis and Catalysis

Volumn 340, Issue 4, 1998, Pages 356-360

  Vilsmaier, Elmar ^a   Milch, Gunther ^a   Roth, Wolfgang ^a   Frank, Walter ^a   Reiß, Guido ^a  

^a Rheinland Pfälzische Technische Universität Kaiserslautern Landau   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0842320949     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. J. Seibel, E. Vilsmaier, in Carbocyclic Three-Membered Ring Compounds, Houben Weyl Methods in Organic Chemistry, Vol E 17b; A. de Meijere, Ed.; Thieme, Stuttgart, 1997, p. 1577
2. E. Vilsmaier, in The Chemistry of the Cyclopropyl Group; Z. Rappoport, Ed.; Wiley Chichester 1987, p. 1341
3. E. Vilsmaier, J. Prakt. Chem. 1994, 336, 396
4. E. Vilsmaier, W. Tröger, M. Gewehr, Angew. Chem. 1981, 93, 277; Angew. Chem. Int. Ed. Engl. 1981, 20, 273
5. E. Vilsmaier, W. Tröger, M. Gewehr, Angew. Chem. 1981, 93, 277; Angew. Chem. Int. Ed. Engl. 1981, 20, 273
6. J. Weidner, E. Vilsmaier, R. Fries, Monatsh. Chem. 1987, 118, 1039
7. E. Vilsmaier, Bull. Soc. Chim. Belg. 1985, 94, 521
8. E. Vilsmaier, W. Tröger, Angew. Chem. 1979, 91, 860; Angew. Chem. Int. Ed. Engl. 1979, 18, 798; E. Vilsmaier, W. Tröger, G. Haag, Chem. Ber. 1981, 114, 67
9. E. Vilsmaier, W. Tröger, Angew. Chem. 1979, 91, 860; Angew. Chem. Int. Ed. Engl. 1979, 18, 798; E. Vilsmaier, W. Tröger, G. Haag, Chem. Ber. 1981, 114, 67
10. E. Vilsmaier, W. Tröger, Angew. Chem. 1979, 91, 860; Angew. Chem. Int. Ed. Engl. 1979, 18, 798; E. Vilsmaier, W. Tröger, G. Haag, Chem. Ber. 1981, 114, 67
11. E. Vilsmaier, K. Joerg, R. Nauert, Chem. Ber. 1984, 117, 2928
12. E. Vilsmaier, W. Tröger, Synthesis 1981, 721
13. V. Butz, E. Vilsmaier, Tetrahedron 1993, 49, 6031
14. E. Vilsmaier, M. Grosse, W.-R. Schlag, G. Milch, U. Bergsträßer, J. prakt. Chem. 1996, 338, 479
15. E. Vilsmaier, G. Milch, U. Bergsträßer, Tetrahedron, in print
16. E. Vilsmaier, T. Herweck, U. Bergsträßer, Tetrahedron, submitted for publication
17. G. Boche, H. M. Walborsky, in Cyclopropane Derived Reactive Intermediates; Z. Rappoport, Ed.; Wiley Chichester 1990, p. 1
18. R. E. Erickson, R. Annino, M. D. Scanlon, G. Zon, J. Am. Chem. Soc. 1969, 91, 1767
19. E. Vilsmaier, T. Stamm, W. Dauth, C. Tetzlaff, S. Barth, Bull. Soc. Chim. Belg. 1992, 100, 37
20. E. Vilsmaier, M. Dotzauer, R. Wagemann, C. Tetzlaff, J. Fath, W.-R. Schlag, U. Bergsträßer, Tetrahedron 1995, 51, 11183
21. C. Tetzlaff, E. Vilsmaier, W.-R. Schlag, Tetrahedron 1990, 46, 8117
22. E. Vilsmaier, C. Tetzlaff, V. Butz, G. Maas, Tetrahedron 1991, 47, 8133
23. E. Vilsmaier, C. M. Klein, W. Tröger, Chem. Ber. 1982, 115, 2795
24. C. Fabre, M. Hadj Ali Salem, Z. Welvart, Bull. Soc. Chim. France 1975, 178
25. E. Vilsmaier, G. Kristen, Chem. Ber. 1982, 115, 1224
26. E. Vilsmaier, J. Fath, G. Maas, Synthesis 1991, 1142
27. E. Vilsmaier, J. Fath, C. Tetzlaff, G. Maas, J. Chem. Soc., Perkin Trans. 2 1993, 1895
28. Calm MP Resonans, Version 2.0, Heratonic Programs, Moscow 1991
29. J. Fath, Dissertation, Universität Kaiserslautern, 1993
30. G. M. Sheldrick, SHELXTL-Plus; Release 4,22. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA
31. Atomic coordinates, bond lengths and angles, and thermal parameters have been deposited at the Cambridge Crystallographic Data Centre, University Chemical Laboratory, Lensfield, Cambridge, CB2 1EW. The X-ray data are available on request from the Director of the CCDC by quoting the full literature citation of this paper.
32. IPDS Software; Version 2.63. Stoe, Darmstadt, Germany, 1996
33. G. M. Sheldrick, SHELXS-86. Program for the Solution of Crystal Structures; University of Göttingen, Germany, 1985
34. G. M. Sheldrick, SHELXL-97. Program for the Refinement of Crystal Structures; University of Göttingen, Germany, 1997