Idioma:

Porphyrins in 1,3-Dipolar Cycloaddition Reactions. Synthesis of New Porphyrin−Chlorin and Porphyrin−Tetraazachlorin Dyads

Silva, Ana M. G ; Lacerda, Paula S. S ; Tomé, Augusto C ; Neves, Maria G. P. M. S ; Silva, Artur M. S ; Cavaleiro, José A. S ; Makarova, Elena A ; Lukyanets, Evgeny A

Journal of organic chemistry, 2006-10, Vol.71 (22), p.8352-8356 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por

Título:
Porphyrins in 1,3-Dipolar Cycloaddition Reactions. Synthesis of New Porphyrin−Chlorin and Porphyrin−Tetraazachlorin Dyads
Autor: Silva, Ana M. G ; Lacerda, Paula S. S ; Tomé, Augusto C ; Neves, Maria G. P. M. S ; Silva, Artur M. S ; Cavaleiro, José A. S ; Makarova, Elena A ; Lukyanets, Evgeny A
É parte de: Journal of organic chemistry, 2006-10, Vol.71 (22), p.8352-8356
Notas: ark:/67375/TPS-SM8GVLJF-P
istex:E3CAE349EA376D23C998BE77C8A3514B99227B58
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Descrição: N-(Porphyrin-2-ylmethyl)glycine was synthesized and used as precursor of azomethine ylide, which was trapped with several dipolarophiles. The reaction of that azomethine ylide with dimethyl fumarate afforded the expected adduct. However, with 1,4-benzo- and 1,4-naphthoquinones only dehydrogenated adducts were isolated. Also, the reaction of that ylide with meso-tetrakis(pentafluorophenyl)porphyrin and tetraazaporphine allowed access to novel porphyrin−chlorin and porphyrin−tetraazachlorin dyads.
Editor: Washington, DC: American Chemical Society
Idioma: Inglês;Russo

Links

Voltar para lista de resultados