2-(6-Methoxy-7-methyl-1,2,3,4-tetrahydro1-naphthyl)ethyl 4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylate

Acta Crystallographica Section C: Crystal Structure Communications

Volumn 52, Issue 9, 1996, Pages 2256-2258

  Noltemeyer, Mathias ^a   Raschke, Thomas ^a   Tietze, Lutz F ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; CONFORMATIONS; CRYSTAL ATOMIC STRUCTURE; DERIVATIVES; ESTERS; ORGANIC ACIDS; SILANES; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

ABSOLUTE CONFIGURATION; CALAMENENE GROUP; CAMPHANIC ACID; ENANTIOSELECTIVE SILANE TERMINATED HECK REACTION; HECK PRODUCT; HYDROBORATION; MOIETY;

AROMATIC HYDROCARBONS;

EID: 0030247565     PISSN: 01082701     EISSN: None     Source Type: Journal    
DOI: 10.1107/S0108270196004167     Document Type: Article

References (13)

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2. Clegg, W. (1981). Acta Cryst. A37, 22-28.
3. Croft, K. D., Ghisalberti, E. L., Hocart, C. H., Jeffries, P. R., Raston, C. L. & White, A. H. (1978). J. Chem. Soc. Perkin Trans, 1, pp. 1267-1270.
4. Flack, H. D. (1983). Acta Cryst. A39, 876-881.
5. Nath, S. C., Bordoloi, M., Shukla, V. & Sharma, R. P. (1989). Phytochemistry, 28, 2007-2037.
6. Sheldrick, G. M. (1990a). Acta Cryst. A46, 467-473.
7. Sheldrick, G. M. (1990b). SHELXTL-Plus. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data. University of Göttingen, Germany.
8. Sheldrick, G. M. (1993). SHELXL93. Program for the Refinement of Crystal Structures. University of Göttingen, Germany.
9. Stoe & Cie (1991a). DIF4. Diffractometer Control Program, Version 7.08. Stoe & Cie, Darmstadt, Germany.
10. Stoe & Cie (1991b). REDU4. Data Reduction Program. Version 7.08. Stoe & Cie, Darmstadt, Germany.
11. Tietze, L. F. & Raschke, T. (1995). Synlett, pp. 597-598.
12. Tietze, L. F. & Schimpf, R. (1994). Angew. Chem. 106, 1138-1139; (1994). Angew. Chem. Int. Ed. Engl. 33, 1089-1091.
13. Tietze, L. F. & Schimpf, R. (1994). Angew. Chem. 106, 1138-1139; (1994). Angew. Chem. Int. Ed. Engl. 33, 1089-1091.