Federico Frateloreto
@fedefrateloreto.bsky.social
Organic Chemist 🧪 | Postdoc at ICIQ in Berrocal Group, Tarragona, Spain 🇪🇸 | PhD at Sapienza Univ. in Di Stefano Group, Rome, Italy 🇮🇹
❗CHECK IT OUT❗
"The Dynamic Chemistry of the Boron–Nitrogen bond" in out in @chemicalscience.rsc.org
Here we achieve Dynamic Libraries exploiting the B←N bond formation/cleavage. The DLs composition can be controlled overtime using an Activated Carboxylic Acid.
pubs.rsc.org/en/Content/A...
"The Dynamic Chemistry of the Boron–Nitrogen bond" in out in @chemicalscience.rsc.org
Here we achieve Dynamic Libraries exploiting the B←N bond formation/cleavage. The DLs composition can be controlled overtime using an Activated Carboxylic Acid.
pubs.rsc.org/en/Content/A...
The dynamic chemistry of the boron–nitrogen bond
Here we report that fully reversible B←N bond formation/cleavage is a promising tool for the achievement of dynamic libraries (DLs) of rapidly interconverting compounds. The composition of a number of...
pubs.rsc.org
December 10, 2025 at 12:08 PM
❗CHECK IT OUT❗
"The Dynamic Chemistry of the Boron–Nitrogen bond" in out in @chemicalscience.rsc.org
Here we achieve Dynamic Libraries exploiting the B←N bond formation/cleavage. The DLs composition can be controlled overtime using an Activated Carboxylic Acid.
pubs.rsc.org/en/Content/A...
"The Dynamic Chemistry of the Boron–Nitrogen bond" in out in @chemicalscience.rsc.org
Here we achieve Dynamic Libraries exploiting the B←N bond formation/cleavage. The DLs composition can be controlled overtime using an Activated Carboxylic Acid.
pubs.rsc.org/en/Content/A...
Reposted by Federico Frateloreto
My recent work is finally out and #openaccess on JOC! @chemistryeurope.bsky.social
We developed a versatile, column chromatography-free methodology to produce a library of organic and water-soluble molecular containers via the Sonogashira coupling reaction. #OrgChem
pubs.acs.org/doi/10.1021/...
We developed a versatile, column chromatography-free methodology to produce a library of organic and water-soluble molecular containers via the Sonogashira coupling reaction. #OrgChem
pubs.acs.org/doi/10.1021/...
A Column Chromatography-Free Protocol for the Synthesis of Water-Soluble Cavitands
An efficient synthetic protocol for the synthesis of a library of unprecedented resorcin[4]arene-based water-soluble molecular containers is reported here. Key to this approach is the tetra-iodo deriv...
pubs.acs.org
July 3, 2025 at 7:59 AM
My recent work is finally out and #openaccess on JOC! @chemistryeurope.bsky.social
We developed a versatile, column chromatography-free methodology to produce a library of organic and water-soluble molecular containers via the Sonogashira coupling reaction. #OrgChem
pubs.acs.org/doi/10.1021/...
We developed a versatile, column chromatography-free methodology to produce a library of organic and water-soluble molecular containers via the Sonogashira coupling reaction. #OrgChem
pubs.acs.org/doi/10.1021/...
Still looking for an easy way to transiently change the conductivity of water? 🧪
Check this out! ⬇️
| Transient Changes in Conductivity of a Water Solution by Means of an Activated Carboxylic Acid (ACA) | ChemSystemsChem
doi.org/10.1002/syst...
Check this out! ⬇️
| Transient Changes in Conductivity of a Water Solution by Means of an Activated Carboxylic Acid (ACA) | ChemSystemsChem
doi.org/10.1002/syst...
Transient Changes in Conductivity of a Water Solution by Means of an Activated Carboxylic Acid (ACA)
Nitroacetic acid, the most active activated carboxylic acid (ACA) employed so far, is used to transiently increase the conductivity of a water solution. Its dissociation produces ions that act as cha....
doi.org
May 14, 2025 at 2:46 PM
Still looking for an easy way to transiently change the conductivity of water? 🧪
Check this out! ⬇️
| Transient Changes in Conductivity of a Water Solution by Means of an Activated Carboxylic Acid (ACA) | ChemSystemsChem
doi.org/10.1002/syst...
Check this out! ⬇️
| Transient Changes in Conductivity of a Water Solution by Means of an Activated Carboxylic Acid (ACA) | ChemSystemsChem
doi.org/10.1002/syst...