Short synthesis of new 13,16-diazaestrone and 13,16-diazaequilenin analogs

Autor: J. A. Parihar, M. M. V. Ramana
Jazyk: angličtina
Rok vydání: 2005
Předmět:
Zdroj: Journal of the Brazilian Chemical Society, Volume: 16, Issue: 4, Pages: 881-883, Published: AUG 2005
Journal of the Brazilian Chemical Society v.16 n.4 2005
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Popis: Different 3-[2-(3,4-dihydro-1-naphthyl)ethyl]imidazolidine-2,4-diones and 3-[2-(1-naphthyl)ethyl]imidazolidine-2,4-diones, when heated in polyphosphoric acid at 150 °C, underwent chemoselective intramolecular cyclization to afford the 13,16-diazaestrone steroids and 13,16- diazaequilenin steroids respectively. Diferentes 3-[2-(3,4-diidro-1-naftil)etil]imidazolidina-2,4-dionas e 3-[2-(1-naftil)etil]- imidazolidina-2,4-dionas, quando aquecidas em ácido polifosfórico a 150 °C, sofrem ciclização quimioseletiva intramolecular resultado nos respectivos esteróides 13,16-diazaestrona e 13,16- diazaequilenina.
Databáze: OpenAIRE