Publication: 1,5-diaza-2,6-diborabicyclo[3.3.0]octadienes: Products of the reactions of trihaloboranes with ketazines
| dc.bibliographiccitation.firstpage | 2477 | |
| dc.bibliographiccitation.issue | 13 | |
| dc.bibliographiccitation.journal | Organometallics | |
| dc.bibliographiccitation.lastpage | 2481 | |
| dc.bibliographiccitation.volume | 19 | |
| dc.contributor.author | Groh, T. | |
| dc.contributor.author | Elter, G. | |
| dc.contributor.author | Noltemeyer, M. | |
| dc.contributor.author | Schmidt, H. G. | |
| dc.contributor.author | Meller, A. | |
| dc.date.accessioned | 2018-11-07T10:43:47Z | |
| dc.date.available | 2018-11-07T10:43:47Z | |
| dc.date.issued | 2000 | |
| dc.description.abstract | The 1,5-diazonia-2,6-diboratabicyclo[3.3.0]octa-1(8),4-dienes 1-4 were prepared from dilithiated ketazines and trihaloboranes, BX3 (X = F, Cl, Br, I). Upon elimination of HX the corresponding 1,5-diaza-2,6-diborabicyclo[3.3.0]octa-3,7-dienes were formed and compounds 5 and 6 (X = Cl, Br) were isolated. Treatment of 5 with MeLi and (BuOLi)-Bu-t, respectively, gave 10 and 11. Monocyclic 1,2,3-azaazoniaborata-5-cyclopentenes (7-9: X = F, Cl, Br) resulted from monolithiated ketazines and BX3. The compounds were characterized by NMR spectroscopy (H-1, B-11, C-13, F-19), MS, and elemental analyses (CH). X-ray crystal structure determinations are presented for 1-4 and 11. | |
| dc.identifier.doi | 10.1021/om0001164 | |
| dc.identifier.isi | 000087804200016 | |
| dc.identifier.uri | https://resolver.sub.uni-goettingen.de/purl?gro-2/47136 | |
| dc.notes.status | zu prüfen | |
| dc.notes.submitter | Najko | |
| dc.publisher | Amer Chemical Soc | |
| dc.relation.issn | 0276-7333 | |
| dc.title | 1,5-diaza-2,6-diborabicyclo[3.3.0]octadienes: Products of the reactions of trihaloboranes with ketazines | |
| dc.type | journal_article | |
| dc.type.internalPublication | yes | |
| dc.type.peerReviewed | yes | |
| dc.type.status | published | |
| dspace.entity.type | Publication |