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meso-Aryl substituted stable unorthodox 5,10-porphodimethenes with α,ß and ß,ß-N-methyl pyrrole connectivities: synthesis and spectroscopic, solid state and theoretical characterization.
Halder, Nyancy; Sangeetha, Mohandas; Usharani, Dandamudi; Rath, Harapriya.
Afiliación
  • Halder N; School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A/2B Raja S.C Mullick Road, Jadavpur, Kolkata, West Bengal 700 032, India. ichr@iacs.res.in.
Org Biomol Chem ; 17(25): 6131-6135, 2019 06 26.
Article en En | MEDLINE | ID: mdl-31179475
A concise and convenient synthetic methodology leading to an unambiguous isolation of two hitherto unknown highly stable single conformers of meso-aryl substituted unorthodox 5,10-porphodimethenes has been developed by the inclusion of N-methyl pyrrole units with α,ß and ß,ß-linkages into the core of heterocyclic macrocycles.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: Reino Unido