One pyrrol with acyl-like substituents you can find in my thesis, but I am not sure that is what you looking for. Groups are too bulky and non-removable.

What is about N-silyl protection? Or NH should be non-protected during electropolymerisation, because it binded with template molecule?

Saeid thanks but this was transformed by bacteria. Andrei thank you but i need in english i am trying to form a functional group on pyrrole and it is not important in which location

Hi Zihni,

N-acylation of pyrrole see in attachment

2- and 3-acetylpyrroles are available from catalogs

Carboxylation is a typical and well-known reaction in the field of pyrroles

Org. Synth. 1971, 51, 100

DOI: 10.15227/orgsyn.051.0100

Is nanoprticles possible of pyrrole ? if yes, then what is range and why which method is possible to synthesis? what is reducing agent?

Z. Onur Uygun Andrei Rogoza Saeid Farsadpour Davide Benedetto Tiz

thank you so much all of you. it is really helpful for me. would you please tell me about new research in organic semiconductors. which organic compound is better in which i can my research.

thank you so much all of you. it is really helpful for me. would you please tell me about new research in organic semiconductors. which organic compound is better in which i can my research. Z. Onur Uygun Andrei Rogoza Saeid Farsadpour Davide Benedetto Tiz