Synthesis and structure elucidation of bromination products from dibromohomobenzonorbornadienes: High temperature bromination - Part 17

Magnetic Resonance in Chemistry

Volumn 43, Issue 1, 2005, Pages 75-81

  Kazaz, Cavit ^a   Daştan, Arif ^a   Balci, Metin ^b  

^a ATATÜRK UNIVERSITY   (Turkey)

^b MIDDLE EAST TECHNICAL UNIVERSITY   (Turkey)

Author keywords

13C NMR; 1H NMR; Bromination; NMR; Polybromides; gauche effect

Indexed keywords

CHLORINE COMPOUNDS; ISOMERS;

13C NMR; 1H NMR; BROMINATION; ELECTROPHILIC ADDITIONS; FORMATION MECHANISM; GAUCHE EFFECTS; HIGHEST TEMPERATURE; POLYBROMIDE; STRUCTURE ELUCIDATION; Γ-GAUCHE EFFECT;

DIHEDRAL ANGLE;

BROMINE DERIVATIVE; NORBORNADIENE DERIVATIVE;

ADDITION REACTION; ARTICLE; BROMINATION; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; HIGH TEMPERATURE; ISOMERISM; STRUCTURE ANALYSIS;

EID: 19044372259     PISSN: 07491581     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrc.1490     Document Type: Article

References (27)

1. Horasan N, Kara Y, Azizoglu A, Balci M. Tetrahedron 2003; 59: 3691.
2. De la Mare PBD, Bolton R. Electrophilic Additions to Unsaturated Systems. Elsewier: New York, 1982; 136.
3. (a) Barkhash VA. Top. Cur. Chem. 1984; 115-117: 1;
4. (b) Çakmak O, Hökelek T, Büyükgüngör O, Balci M. Tetrahedron Lett. 1990; 31: 2345;
5. (c) Çakmak O, Balci M. J. Org. Chem. 1989; 54: 181;
6. (d) Dastan A. Turk. J Chem. 2003; 27: 181.
7. (a) Dastan A, Balci M, Hökelek T, Ülkü D, Büyükgüngör O. Tetrahedron 1994; 50: 10555;
8. (b) Dastan A, Demir Ü, Balci M. J. Org. Chem. 1994; 59: 6534;
9. (c) Tutar A, Taskesenligil Y, Cakmak O, Abbasoglu R, Balci M. J. Org. Chem. 1996; 61: 8297;
10. (d) Menzek A, Saracoglu N, Dastan A, Balci M, Abbasoglu R. Tetrahedron 1997; 53: 14451;
11. (e) Altundas A, Dastan A, McKee MM, Balci M. Tetrahedron 2000; 56: 6115;
12. (f) Dastan A, Uzundumlu E, Balci M. Helv. Chim. Acta 2002; 81: 2729;
13. (g) Dastan A. J. Chem. Res. (S) 2002; 591;
14. (h) Dastan A. Turk. J. Chem. 2002; 26: 535.
15. Dastan A, Taskesenligil Y, Tümer F, Balci M. Tetrahedron 1996; 52: 14005.
16. Cakmak O, Taskesenligil Y, Balci M. J. Org. Chem. 1992; 56: 3442.
17. Tutar A, Balci M. Tetrahedron 2002; 58: 8979.
18. (a) Smith WB. J. Org. Chem. 1984; 49: 3771;
19. (b) Lobanova TP, Derendyaev BG, Kollegova MI, Barkash VA. Zh. Org. Khim. (Engl. Transl.) 1973; 9: 1883.
20. Karplus M. J. Am. Chem. Soc. 1963; 85: 2870.
21. (a) Paquette LA, Volz WE. J. Am. Chem. Soc. 1976; 98: 2910;
22. (b) Jefford CW, Ramey KC. Tetrahedron 1968; 24: 2927.
23. (a) Dalling DK, Grant DM. J. Am. Chem. Soc. 1967; 89: 6612;
24. (b) Dorman DE, Roberts JD. J. Am. Chem. Soc. 1970; 92: 1355;
25. (c) Gheorghiu MD, Olteanu E. J. Org. Chem. 1987; 52: 5158.
26. Tori K, Ueyama M, Tsuji T, Matsumura H, Tanida H, Iwamura H, Kushida K, Nishida T, Satoh S. Tetrahedron Lett. 1974; 15: 327.
27. Winstein S. J. Am. Chem. Soc. 1961; 83: 1516.