2026-05-05T21:03:50Zhttps://uvadoc.uva.es/oai/requestoai:uvadoc.uva.es:10324/745142025-01-28T20:04:01Zcom_10324_1187com_10324_931com_10324_894col_10324_1408
Modular De novo Synthesis of Unsymmetrical BODIPY Dyes Possessing Four Different Aryl Substituents
Netz, Natalie
Díez Poza, Carlos
Barbero Pérez, María Asunción
Opatz, Till
A modular synthesis of unsymmetrical BODIPY dyes
based on a [6π] electrocyclization to construct both pyrrole
rings is presented. The products carry four aryl moieties in positions
1, 3, 5, and 7, which can be freely selected, as well as optional substitution in positions 2 and 8. The method employs acetophenones, benzaldehydes as well as glycine nitrile or
glycine ethyl ester as the key building blocks.
2025-01-28
2025-01-28
2017
9999-01-01
info:eu-repo/semantics/article
European Journal of Organic Chemistry, 2017(31), 4580-4599.
1434-193X
https://uvadoc.uva.es/handle/10324/74514
10.1002/EJOC.201700773
4580
31
4599
European Journal of Organic Chemistry
2017
1099-0690
eng
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700773
info:eu-repo/semantics/restrictedAccess
John Wiley & Sons, Inc
John Wiley & Sons, Inc