Publication: sigma-bishomoaromatic heterocycles: Reactivity and synthesis of 3-oxatetracyclo[3.3.0.0(2,8)0(4,6)]octane by photolysis at 185 nm
| dc.contributor.authors | Klarner, FG; Golz, T; Uhlander, C; Yaslak, S | |
| dc.date.accessioned | 2022-03-12T16:56:44Z | |
| dc.date.accessioned | 2026-01-10T17:31:46Z | |
| dc.date.available | 2022-03-12T16:56:44Z | |
| dc.date.issued | 1996 | |
| dc.description.abstract | The title compound 5 was produced by 185 nm photolysis of 8. The products of the 185 nm photolysis can be rationalized by the assumption of the two diradical intermediates 16 and 17. Ar a temperature between 150 and 200 degrees C 5 reacts with fumaronitrile 23 to give the adducts 7 and 26 in a ratio of about (5 : 1). The kinetic analysis of this reaction shows, that the adduct 7 is formed by 1.3 dipolar cycloaddition of intermediate carbonyl ylide 6. | |
| dc.identifier.doi | 10.1016/0040-4039(96)00062-7 | |
| dc.identifier.issn | 0040-4039 | |
| dc.identifier.uri | https://hdl.handle.net/11424/226829 | |
| dc.identifier.wos | WOS:A1996TY29300017 | |
| dc.language.iso | eng | |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | |
| dc.relation.ispartof | TETRAHEDRON LETTERS | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | PHOTOCHEMISTRY | |
| dc.subject | OXIDES | |
| dc.title | sigma-bishomoaromatic heterocycles: Reactivity and synthesis of 3-oxatetracyclo[3.3.0.0(2,8)0(4,6)]octane by photolysis at 185 nm | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 1388 | |
| oaire.citation.issue | 9 | |
| oaire.citation.startPage | 1385 | |
| oaire.citation.title | TETRAHEDRON LETTERS | |
| oaire.citation.volume | 37 |
