| dc.contributor.author | Yildirim, SO | |
| dc.contributor.author | Akkurt, M | |
| dc.contributor.author | Baran, A | |
| dc.contributor.author | Secen, H | |
| dc.contributor.author | Büyükgüngör, Orhan | |
| dc.date.accessioned | 2020-06-21T15:36:51Z | |
| dc.date.available | 2020-06-21T15:36:51Z | |
| dc.date.issued | 2005 | |
| dc.identifier.issn | 2056-9890 | |
| dc.identifier.uri | https://doi.org/10.1107/S160053680501398X | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/21071 | |
| dc.description | Secen, Hasan/0000-0002-5388-6111 | en_US |
| dc.description | WOS: 000229464500162 | en_US |
| dc.description.abstract | The title compound, (2-exo, 7-exo, 9-exo, 10-exo)-11-oxatricyclo[ 6.2.1.0(2,7)] undec-4-ene-9,10-diyl diacetate, C14H18O5, was synthesized in the same way as its 9-endo, 10-endo isomer. The X-ray study showed that the Diels-Alder reaction of 5-exo, 6-exo-diacetato-7-oxabicylclo[2.2.1] hepta-2-ene with 3-sulfolene, a protected 1,3- butadiene, yields the 2-exo, 7-exo product, i. e. reacts in the same way as the 5-endo, 6-endo isomer of the starting compound. Intermolecular C-H center dot center dot center dot O interactions link the molecules into infinite chains extending along the b axis of the monoclinic crystal structure. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Int Union Crystallography | en_US |
| dc.relation.isversionof | 10.1107/S160053680501398X | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | The 2-exo,7-exo,10-exo isomer of 11-oxa-tricycolo[6.2.1.0(2,7)]undec-4-ene-9,10-diyl diacetate | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 61 | en_US |
| dc.identifier.startpage | O1677 | en_US |
| dc.identifier.endpage | O1679 | en_US |
| dc.relation.journal | Acta Crystallographica Section E-Crystallographic Communications | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
