Margherita Miele - Concepedia

Author

Margherita Miele

University of Vienna ORCID

Also Known As

Margherita Miele, Miele, Margherita

Publications

366

Citations

H-Index

Concepts

All Affiliations

University of Vienna University of Turin University of Messina University of Milan

About

Margherita Miele is an author at University of Vienna specializing in organic chemistry, chemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	3	3	80
2	Natural Sciences	3	3	80
3	Biomolecular Engineering	3	3	76
4	Biochemistry	2	2	51
5	Chemical Engineering	1	1	18

Margherita Miele

Publications

316

Citations

H-Index

Page 1

	Year	Citations
Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF<sub>2</sub>-Carbene Equivalent Margherita Miele, Andrea Citarella, Nicola Micale, Organic Letters	2019	78
Highly chemoselective difluoromethylative homologation of iso(thio)cyanates: expeditious access to unprecedented α,α-difluoro(thio)amides Margherita Miele, Rosarita D’Orsi, Vellaisamy Sridharan, Chemical Communications	2019	42
Chemoselective Homologation–Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (<i>n+1</i>)-Halomethyl-Alkanes Margherita Miele, Andrea Citarella, Thierry Langer, Organic Letters	2020	37
Chemoselective reduction of isothiocyanates to thioformamides mediated by the Schwartz reagent Karen de la Vega‐Hernández, Raffaele Senatore, Margherita Miele, Organic & Biomolecular Chemistry EngineeringBiochemistrySchwartz ReagentNatural SciencesOrganic Chemistry	2018	33
Carbenoid-Mediated Homologation Tactics for Assembling (Fluorinated) Epoxides and Aziridines Laura Ielo, Vittorio Pace, Veronica Pillari, Synlett Homologation StrategiesEngineeringAlkene MetathesisNatural SciencesDiversity-oriented Synthesis	2020	29
Taking advantage of lithium monohalocarbenoid intrinsic α-elimination in 2-MeTHF: controlled epoxide ring-opening <i>en route</i> to halohydrins Laura Ielo, Margherita Miele, Veronica Pillari, Organic & Biomolecular Chemistry	2021	22
Consecutive C1‐Homologation / Displacement Strategy for Converting Thiosulfonates into <i>O,S‐</i>Oxothioacetals Laura Ielo, Veronica Pillari, Margherita Miele, Advanced Synthesis & Catalysis Chemical EngineeringEngineeringChemical TransformationBiochemistryNatural Sciences	2020	18
(Difluoromethyl)trimethylsilane (TMSCHF2): A Useful Difluoromethylating Nucleophilic Source Margherita Miele, Vittorio Pace Australian Journal of Chemistry	2021	16
Recent advances in the synthesis and reactivity of spiro-epoxyoxindoles Serena Monticelli, Laura Castoldi, Saad Touqeer, Chemistry of Heterocyclic Compounds Synthetic ChemistryRecent AdvancesBiomolecular Engineering	2018	14
Straightforward synthesis of bench-stable heteroatom-centered difluoromethylated entities <i>via</i> controlled nucleophilic transfer from activated TMSCHF<sub>2</sub> Margherita Miele, Laura Castoldi, Xenia Simeone, Chemical Communications	2022	14

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