Federico Casti

Dr. Federico Casti

Università degli studi di Cagliari, Cagliari, Sardegna, Italy
orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 March 2022 in Molecules
Verified
Journal Article
Open access
PDF file
FCFederico Casti
Federico Casti
FBFrancesco Basoccu
Francesco Basoccu
RMRita Mocci
Rita Mocci
LLLidia De Luca
Lidia De Luca
APAndrea Porcheddu
Andrea Porcheddu
FCFederico Cuccu
Federico Cuccu
In just a few years, chemists have significantly changed their approach to the synthesis of organic molecules in the laboratory and industry. Researchers are encouraged to approach “greener” reagents, solvents, and methodologies, to go hand in hand with the world’s environmental matter, such as water, soil, and air pollution. The employment of plant and animal derivates that are commonly regarded as “waste material” has paved the way for the development of new green strategies. In this review, the most important innovations in this field have been highlighted, paying due attention to those materials that have played a crucial role in organic reactions: wool, silk, and feather. Moreover, we decided to focus on the other most important supports and catalysts in green syntheses, such as proteins and their derivates. Different materials have shown prominent activity in the adsorption of metals and organic dyes, which has constituted a relevant scope in the last two decades. We intend to furnish a complete screening of the application given to these materials and contribute to their potential future utilization.

5 April 2022 in Beilstein Archives
Verified
Preprint
Open access
PDF file
FBFrancesco Basoccu
Francesco Basoccu
FCFederico Cuccu
Federico Cuccu
FCFederico Casti
Federico Casti
RMRita Mocci
Rita Mocci
CFClaudia Fattuoni
Claudia Fattuoni
APAndrea Porcheddu
Andrea Porcheddu
Isocyanides are hardly-to-produce, dramatically sensitive to purification processes and complex to handle as synthetic tools. Notwithstanding this, they represent one of the most refined and valuable compounds for accessing sophisticated and elegant synthetic routes. A unique interest has always been addressed to their production, though their synthetic pathways usually involve employing strong conditions and toxic reagents. The current paper intends to provide a conceptually innovative synthetic protocol designed for mechanochemical isocyanide preparation, simultaneously lowering the related reagents' toxicity and improving their purification in a straightforward procedure.