78283-13-3Relevant academic research and scientific papers
N-AMINO ESTERS (BMMA): NOVEL REAGENTS FOR ANNELATION OF PYRIMIDINE MOIETIES
Sauter, Fritz,Froehlich, Johannes,Blasl, Karin,Gewald, Karl
, p. 851 - 866 (1995)
New reagents for heterocyclic annelations containing a N-amino moiety (=BMMA) were developed and studied regarding their scope and limitations: one-pot reaction with (hetero)aromatic ortho-aminocarbonyl-type model compounds ("car
Microwave-mediated solventless synthesis of new derivatives of marine alkaloid Leucettamine B
Chérouvrier, Jean-René,Carreaux, Fran?ois,Bazureau, Jean Pierre
, p. 3581 - 3584 (2007/10/03)
New access to N-alkyl derivatives of the marine alkaloid Leucettamine B are described using two three-step convergent routes. For the formation of the 2-amino imidazolone ring, the key steps involve solvent-free condensations under microwaves and guanylation reactions with non-sterically hindered primary amines.
Reactions of Amino Acids on 2-Methylmercaptohydantoin Derivatives. Synthesis of Imidazoimidazoline and Imidazoquinazoline Derivatives
Daboun, H. A.,Abd-Elfattah, A. M.,Hussein, M. M.,Shalaby, A. F. A.
, p. 366 - 369 (2007/10/02)
Treatment of 5-arylidene-2-methylmercaptohydantoins (1a-d) and 5-arylazo-2-methylmercaptohydantoins (3a, b) with glycine in acetic acid gave 5-arylidene-N2-carboxymethylglycocyamidines (2a-d) and 5-arylazo-N2-carboxymethylglycocyamid
