Pregled bibliografske jedinice broj: 1835
A facile, general route to adamantanophanes. Synthesis and conformational behavior of [4.4](1,3)Adamantanophan-trans,trans-1,8-diene
A facile, general route to adamantanophanes. Synthesis and conformational behavior of [4.4](1,3)Adamantanophan-trans,trans-1,8-diene // Tetrahedron letters, 37 (1996), 28; 4829-4832 doi:10.1016/0040-4039(96)00523-0 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1835 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A facile, general route to adamantanophanes. Synthesis and conformational behavior of [4.4](1,3)Adamantanophan-trans,trans-1,8-diene
Autori
Mlinarić-Majerski, Kata ; Pavlović, Dražen ; Marinić, Željko
Izvornik
Tetrahedron letters (0040-4039) 37
(1996), 28;
4829-4832
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Ramber-Backlund rearrangement ; [m.n]adamantanophanes ; dynamic NMR spectroscopy
Sažetak
Ramber-Backlund rearrangement of disulfone 2 leads to the ring-contracted 4, 6:11, 13-di(1, 3-adamantano)cyclotetradeca-trans, trans-1, 8-diene (3a) along with 4, 6:11, 13-di(1, 3-adamantano)cyclotetradeca-cis, trans-1, 8-diene (3b! ) and 4, 6:12, 14-di(1, 3-adamantano)-8, 10-dehydro-9, 9-dichlorocyclopentadeca-1-diene (4) as a minor products. The ring inversion of 3a can most reasonably be interpreted in terms of equilibrium process between two conformers with effective C-2h symmetry.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- Chemical Abstracts
