4-cyclohexanespiro{3-[2-methoxy-2-(2,6-dimethoxyphenyl)ethenyl]oxetan-2- one}

Acta Crystallographica Section C: Crystal Structure Communications

Volumn 53, Issue 6, 1997, Pages 746-748

  Kennedy, Alan R ^a   Kerr, William J ^a   McKendry, Sharon ^a  

^a UNIVERSITY OF STRATHCLYDE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CHEMICAL BONDS; CONFORMATIONS; ISOMERIZATION; MOLECULAR CRYSTALS; MOLECULAR STRUCTURE; SYNTHESIS (CHEMICAL);

LACTONES; STEREOISOMERIC PRODUCTS;

KETONES;

EID: 0031165818     PISSN: 01082701     EISSN: None     Source Type: Journal    
DOI: 10.1107/S0108270197001418     Document Type: Article

References (11)

1. Adam, W., Albert, R., Grau, N. D., Hasemann, L., Nestler, B., Peters, E.-M., Peters, K., Prechtl, F. & von Schnering, H. G. (1991). J. Org. Chem. 56, 5778-5781.
2. Allen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1-S19.
3. Burla, M. C., Camalli, M., Cascarano, G., Giacovazzo, C., Polidori, G., Spagna, R. & Viterbo, D. (1989). J. Appl. Cryst. 22, 389-393.
4. Dou, S., Basaran, R., Paulus, H. & Weiss, A. (1993). Z. Naturforsch. Teil A, 48, 491-496.
5. Harrity, J. P. A., Heron, N. M., Kerr, W. J., McKendry, S., Middlemiss, D. & Scott, J. S. (1996). Synlett, pp. 1184-1186.
6. Harrity, J. P. A., Kerr, W. J., Middlemiss, D. & Scott, J. S. (1997). J. Organomet. Chem. 503. In the press.
7. Hegmann, J., Christi, M., Peters, K., Peters, E.-M. & von Schnering, H. G. (1987). Tetrahedron Lett. 28, 6429-6432.
8. Johnson, C. K. (1976). ORTEPII. Report ORNL-5138. Oak Ridge National Laboratory, Tennessee, USA.
9. Molecular Structure Corporation (1988). MSC/AFC Diffractometer Control Software. MSC, 3200 Research Forest Drive, The Woodlands, TX 77381, USA.
10. Molecular Structure Corporation (1992). TEXSAN. Single Crystal Structure Analysis Software. MSC, 3200 Research Forest Drive, The Woodlands, TX 77381, USA.
11. Zachariasen, W. H. (1968). Acta Cryst. A24, 212-216.