-transparent.png){kind=logo}
This paper reports the synthesis of a novel class of macrocyclic tetraesters containing 1,3-butandiol sub-units by reacting the stannolan derivative of the diol with diacyl chloride. The structure of the possible isomers was assigned by spectroscopic data and comparison with samples otherwise prepared. Preliminary screening revealed that these compounds have low antimicrobial activity, although it is higher than that of the starting diol.
Related Publications
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
July 2009,
European journal of medicinal chemistry,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
January 2010,
Acta poloniae pharmaceutica,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
June 2009,
Journal of enzyme inhibition and medicinal chemistry,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
April 2005,
Archiv der Pharmazie,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
October 2022,
Molecules (Basel, Switzerland),
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
January 1989,
Zentralblatt fur Mikrobiologie,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
January 1984,
Pharmaceutica acta Helvetiae,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
June 2013,
Bioorganic & medicinal chemistry,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
January 2002,
Bollettino chimico farmaceutico,
A M Fadda, and
A M Maccioni, and
E Maccioni, and
G Podda
February 2011,
Bioorganic & medicinal chemistry letters,
