A facile synthesis of two brucine-steroid derivatives

Lauro Figueroa-Valverde, Francisco Díaz-Cedillo, Elodia Garcia-Cervera, Maria Lopez-Ramos, Eduardo Pool-Gomez

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

In this study, two brucine-steroid derivative were synthesized. In first stage, the brucine-androsterone derivative was development by the reaction of N1-(2,3-dimethoxystrychnidin-10-yliden)-ethane-1,2-diamine and androsteronehemisuccinate using as catalyst a carbodiimide derivative. The second stage was achieved by the reaction of N1-(2,3-dimethoxystrychnidin-10- yliden)-ethane-1,2-diamine with b-estradiol 17-hemisuccinate to form the brucine-estradiol conjugatein presence of a carbodiimide derivative.In conclusion, in this study we show a facile procedure for synthesis of two brucine-steroid derivatives.

Original languageEnglish
Pages (from-to)1901-1904
Number of pages4
JournalAsian Journal of Chemistry
Volume25
Issue number4
DOIs
StatePublished - 2013

Keywords

  • 17-β-Estradiol
  • Androsterone
  • Brucine
  • Carbodiimide

Fingerprint

Dive into the research topics of 'A facile synthesis of two brucine-steroid derivatives'. Together they form a unique fingerprint.

Cite this