| dc.contributor.author | Yıldız, Yaşar Kemal | |
| dc.contributor.author | Öztürk, Turan | |
| dc.contributor.author | Balcı, Metin | |
| dc.date.accessioned | 2019-10-17T07:45:09Z | |
| dc.date.available | 2019-10-17T07:45:09Z | |
| dc.date.issued | 1999 | en_US |
| dc.identifier.issn | 0040-4020 | |
| dc.identifier.uri | http.//10.1016/S0040-4020(99)00493-7 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/7697 | |
| dc.description | Yıldız, Yaşar Kemal (Balikesir Author) | en_US |
| dc.description.abstract | 8-brom-6,7-dihydrobenzocycloheptene 16 and 9-bromo-6,7-benzocycloheptadiene 17 have been synthesized via a new and simple method, and their allene reactions were studied. Treatment of 16 with a base in the presence of DPIBF (diphenylisobenzofuran) gave the strained bicyclic allene 9, which underwent a cycloaddition reaction to yield 25 and 26. On the other hand, the reaction of the vinyl bromide 17 with a base, either in the presence or absence of DPIBF, resulted in the formation of 7H-benzocycloheptadiene 21, rather than the alkyne 22. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Pergamon-Elsevier Science Ltd | en_US |
| dc.relation.isversionof | 10.1016/S0040-4020(99)00493-7 | en_US |
| dc.rights | info:eu-repo/semantics/embargoedAccess | en_US |
| dc.subject | Derivatives | en_US |
| dc.title | Trapping of 1,2-benzo-1,3,4-cycloheptatriene as evidence for a strained cyclic allene structure | en_US |
| dc.type | article | en_US |
| dc.relation.journal | Tetrahedron | en_US |
| dc.contributor.department | Necatibey Eğitim Fakültesi | en_US |
| dc.identifier.volume | 55 | en_US |
| dc.identifier.issue | 30 | en_US |
| dc.identifier.startpage | 9317 | en_US |
| dc.identifier.endpage | 9324 | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
