What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of study are Organic chemistry, Aryl, Medicinal chemistry, Enantioselective synthesis and Catalysis.
His Organic chemistry and Diselenide, Nucleophilic substitution, Selenium, Alkylation and Nucleophile investigations all form part of his Organic chemistry research activities.
In his study, Zinc, Stereospecificity, Walden inversion and Combinatorial chemistry is strongly linked to Halide, which falls under the umbrella field of Aryl.
His work carried out in the field of Medicinal chemistry brings together such families of science as Sodium methoxide, Ion, Methoxide, Diphenyl diselenide and Ketone.
Marcello Tiecco has researched Enantioselective synthesis in several fields, including Thiourea, Organoselenium Compound and Bifunctional.
His Electrophile research is multidisciplinary, relying on both Yield, Reagent and Methanol.
His most cited work include:
- Asymmetric Azidoselenenylation of Alkenes: A Key Step for the Synthesis of Enantiomerically Enriched Nitrogen‐Containing Compounds (97 citations)
- Novel azido-phenylselenenylation of double bonds. Evidence for a free-radical process (93 citations)
- Electrophilic Selenium, Selenocyclizations (93 citations)
What are the main themes of his work throughout his whole career to date?
Organic chemistry, Medicinal chemistry, Selenium, Reagent and Electrophile are his primary areas of study.
He performs integrative study on Organic chemistry and Ammonium persulfate in his works.
Marcello Tiecco has included themes like Alkylation, Radical, Homolysis, Stereochemistry and Nucleophile in his Medicinal chemistry study.
His research integrates issues of Intramolecular force, Ring and Nucleophilic substitution in his study of Nucleophile.
His Reagent study combines topics in areas such as Selectivity and Addition reaction.
His studies deal with areas such as Combinatorial chemistry, Regioselectivity, Methanol and Diselenide as well as Electrophile.
He most often published in these fields:
- Organic chemistry (49.69%)
- Medicinal chemistry (37.42%)
- Selenium (20.25%)
What were the highlights of his more recent work (between 2007-2012)?
- Organic chemistry (49.69%)
- Selenium (20.25%)
- Catalysis (12.27%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Organic chemistry, Selenium, Catalysis, Reagent and Enantioselective synthesis.
In his works, Marcello Tiecco conducts interdisciplinary research on Organic chemistry and Ammonium persulfate.
In general Selenium, his work in Phenylselenol is often linked to Amino acid derivative linking many areas of study.
His Catalysis research integrates issues from Organoselenium Compound, Aryl, XPhos, Diphenyl diselenide and Oxidizing agent.
The concepts of his Reagent study are interwoven with issues in Electrophile, Copper, Combinatorial chemistry, Nucleophile and Addition reaction.
In general Enantioselective synthesis study, his work on Desymmetrization often relates to the realm of Silanes, thereby connecting several areas of interest.
Between 2007 and 2012, his most popular works were:
- Eco‐Friendly Olefin Dihydroxylation Catalyzed by Diphenyl Diselenide (80 citations)
- Preparation of the First Bench‐Stable Phenyl Selenolate: an Interesting “On Water” Nucleophilic Reagent (64 citations)
- A New Stereoselective Synthesis of Cyclopropanes Containing Quaternary Stereocentres via Organocatalytic Michael Addition to Vinyl Selenones (52 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Marcello Tiecco mainly focuses on Organic chemistry, Catalysis, Michael reaction, Selenium and Enantioselective synthesis.
Reagent, Bifunctional, Acylation, Enantiopure drug and Stereoisomerism are subfields of Organic chemistry in which his conducts study.
His Catalysis research is multidisciplinary, incorporating perspectives in Aryl, XPhos and Diphenyl diselenide.
His Selenium study frequently draws parallels with other fields, such as Electrophile.
His Enantioselective synthesis course of study focuses on Organoselenium Compound and Desymmetrization, Optically active, Squaramide and Cinchona.
His Nucleophilic addition study combines topics from a wide range of disciplines, such as Ketone and Medicinal chemistry.
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