메뉴 건너뛰기




Volumn 215, Issue 4, 2000, Pages 529-530

Crystal structure of 2,2-exo-3,5,5-exo-6-hexabromobicycloheptane, C7H6Br6

Author keywords

[No Author keywords available]

Indexed keywords


EID: 23044523220     PISSN: 14337266     EISSN: None     Source Type: Journal    
DOI: 10.1515/ncrs-2000-0432     Document Type: Article
Times cited : (5)

References (20)
  • 1
    • 0001344370 scopus 로고
    • Electrophilic additions to strained olefins
    • Traylor, T. G.: Electrophilic additions to strained olefins. Acc. Chem. Res. 2 (1969) 152-160.
    • (1969) Acc. Chem. Res. , vol.2 , pp. 152-160
    • Traylor, T.G.1
  • 2
    • 33947474820 scopus 로고
    • Bicycloheptadiene dibromides
    • Winstein, S.: Bicycloheptadiene dibromides. J. Am. Chem. Soc. 83 (1961) 1516-1517.
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 1516-1517
    • Winstein, S.1
  • 3
    • 0000954394 scopus 로고
    • High functionalized benzobarrelene derivatives - Bromination of 2-bromo-5,6-benzobicyclo(2.2.2)octa-2,6-diene. High-temperature bromination 3
    • Balci, M.; Çakmak, O.; Hökelek, T.: High functionalized benzobarrelene derivatives - bromination of 2-bromo-5,6-benzobicyclo(2.2.2)octa-2,6-diene. High-temperature bromination 3. J. Org. Chem. 57 (1992a) 6640-6643.
    • (1992) J. Org. Chem. , vol.57 , pp. 6640-6643
    • Balci, M.1    Çakmak, O.2    Hökelek, T.3
  • 4
    • 21044458332 scopus 로고
    • Synthesis of 2,3-disubstituted-benzobarrelenes, 2,5-disubstituted-benzobarrelenes and 2,6-disubstituted- Benzobarrelenes
    • Balci, M.; Çakmak, O.; Hökelek, T.: Synthesis of 2,3-disubstituted-benzobarrelenes, 2,5-disubstituted-benzobarrelenes and 2,6-disubstituted- benzobarrelenes. Tetrahedron. 48 (1992b) 2163-2182.
    • (1992) Tetrahedron. , vol.48 , pp. 2163-2182
    • Balci, M.1    Çakmak, O.2    Hökelek, T.3
  • 5
    • 0000449208 scopus 로고
    • Chlorocyanation of barrelenes as a route to 1-cyanosemibullvalenes. Convenient introduction of an efficient π-electron acceptor substituent and its influence on the cope equilibrium
    • Paquette, L. A.; Volz, W. E.: Chlorocyanation of barrelenes as a route to 1-cyanosemibullvalenes. Convenient introduction of an efficient π-electron acceptor substituent and its influence on the cope equilibrium. J. Am. Chem. Soc. 98 (1976) 2910-2917.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2910-2917
    • Paquette, L.A.1    Volz, W.E.2
  • 7
    • 0039413710 scopus 로고    scopus 로고
    • Structure of exo,exo-2,3-endo, endo-5,6-tetrabromobicycloheptane
    • Hökelek, T.; Çakmak, O.; Tutar, A.: Structure of exo,exo-2,3-endo, endo-5,6-tetrabromobicycloheptane. J. Chem. Crystallogr. 28 (1998) 433-436.
    • (1998) J. Chem. Crystallogr. , vol.28 , pp. 433-436
    • Hökelek, T.1    Çakmak, O.2    Tutar, A.3
  • 8
    • 21044435562 scopus 로고
    • Crystal and molecular structure of exo-2, exo-3-dicholoro-endo-5,6-(orthophenylene)norbornane
    • Baker, R.; Wood, J. S.: Crystal and molecular structure of exo-2, exo-3-dicholoro-endo-5,6-(orthophenylene)norbornane. J. Chem. Soc. Perkin Trans. 2 (1978) 971-974.
    • (1978) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 971-974
    • Baker, R.1    Wood, J.S.2
  • 10
    • 0000839950 scopus 로고
    • Electronic control of stereoselectivity 30 x-ray analysis of the effect of apical substitution on the 3-dimensional features of isodicyclopentafulvenes. Experimental demonstration of minimal bridgehead C-H angle deformation accompanying substantial hybridization change at the apical center
    • Gallucci, J. C.; Kravetz, T. M.; Green, K. E.; Paquette, L. A.: Electronic control of stereoselectivity 30 x-ray analysis of the effect of apical substitution on the 3-dimensional features of isodicyclopentafulvenes. Experimental demonstration of minimal bridgehead C-H angle deformation accompanying substantial hybridization change at the apical center. J. Am. Chem. Soc. 107 (1985) 6592-6598.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 6592-6598
    • Gallucci, J.C.1    Kravetz, T.M.2    Green, K.E.3    Paquette, L.A.4
  • 11
    • 21044443360 scopus 로고
    • Stereochemistry of rings. XVII. Norbornane derivatives 1. 2-(p-Methoxyphenyl)-3-phenylbicyclo[2.2.1]heptane (I) and 2-(p-Nitrophenyl)-3-phenylbicyclo[2.2.1]heptane (II)
    • Bocelli, G.: Stereochemistry of rings. XVII. Norbornane derivatives 1. 2-(p-Methoxyphenyl)-3-phenylbicyclo[2.2.1]heptane (I) and 2-(p-Nitrophenyl)-3-phenylbicyclo[2.2.1]heptane (II). Acta Crystallogr. C46( 1990) 256-259.
    • (1990) Acta Crystallogr. , vol.C46 , pp. 256-259
    • Bocelli, G.1
  • 13
    • 1842692143 scopus 로고
    • A General definition of ring puckering coordinates
    • Cremer, D.; Pople, J. A.: A General definition of ring puckering coordinates. J. Am. Chem. Soc. 97 (1975) 1354-1358.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1354-1358
    • Cremer, D.1    Pople, J.A.2
  • 15
    • 0002365147 scopus 로고    scopus 로고
    • Structure of exo,endo, exo,exo-2,3,5,6-tetrabromonorbornane
    • Çelik, I.; Akkurt, M.; Ide, S.; Çakmak, O.: Structure of exo,endo, exo,exo-2,3,5,6-tetrabromonorbornane. Z. Kristallogr. 214 (1999) 410-412.
    • (1999) Z. Kristallogr. , vol.214 , pp. 410-412
    • Çelik, I.1    Akkurt, M.2    Ide, S.3    Çakmak, O.4
  • 20
    • 0001117612 scopus 로고
    • PARST95: A system of Fortran routines for calculating molecular structure parameters from the results of crystal structure analyses
    • Nardelli, M.: PARST95: A system of Fortran routines for calculating molecular structure parameters from the results of crystal structure analyses. J. Appl. Crystallogr. 28 (1995) 659.
    • (1995) J. Appl. Crystallogr. , vol.28 , pp. 659
    • Nardelli, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.