Idioma:

Facile synthetic routes to bridge-functionalised calix[4]arenes

Fong, Angela ; Campbell, Cameron L ; Huynh, Silvia ; McCormick McPherson, Laura J ; Teat, Simon J ; Bebbington, Magnus W. P ; Dalgarno, Scott J

Chemical communications (Cambridge, England), 2022-03, Vol.58 (2), p.332-335 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por

Título:
Facile synthetic routes to bridge-functionalised calix[4]arenes
Autor: Fong, Angela ; Campbell, Cameron L ; Huynh, Silvia ; McCormick McPherson, Laura J ; Teat, Simon J ; Bebbington, Magnus W. P ; Dalgarno, Scott J
Assuntos: Aromatic compounds ; Furans ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY ; Ring opening
É parte de: Chemical communications (Cambridge, England), 2022-03, Vol.58 (2), p.332-335
Notas: For ESI and crystallographic data in CIF or other electronic format see DOI
2126914-2126920
Electronic supplementary information (ESI) available: Synthetic, analytical and crystallographic information (CIFs). CCDC
10.1039/d1cc06889j
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
AC02-05CH11231
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Engineering and Physical Sciences Research Council (EPSRC)
Descrição: Ring-opening of furans at the equatorial methylene bridge positions of a calix[4]arene gives access to a range of new molecules (in good yield) that have widespread potential impact in supramolecular chemistry amongst other areas. Facile synthetic alteration of the calix[4]arene methylene bridges provides access to a range of new molecules whilst preserving the characteristics of this extremely versatile host framework.
Editor: England: Royal Society of Chemistry
Idioma: Inglês

Links

Voltar para lista de resultados

Anterior Resultado 5 Avançar Ir para próxima página