Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Margherita Miele"'
Publikováno v:
Molecules, Vol 27, Iss 19, p 6701 (2022)
The necessity of more sustainable conditions that follow the twelve principles of Green Chemistry have pushed researchers to the development of novel reagents, catalysts and solvents for greener asymmetric methodologies. Solvents are in general a fun
Externí odkaz:
https://doaj.org/article/6f145a95fbc64d289d64f7cd55d48094
Publikováno v:
Homologation Reactions. :79-142
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-17
Publikováno v:
Chemical communications (Cambridge, England). 58(38)
The commercially available and experimentally convenient (bp 65 °C) difluoromethyltrimethylsilane (TMSCHF
Publikováno v:
Synlett. 32:551-560
Homologation strategies provide highly versatile tools in organic synthesis for the introduction of a CH2 group into a given carbon skeleton. The operation can result in diverse structural motifs by tuning of the reaction conditions and the nature of
Publikováno v:
Greener Synthesis of Organic Compounds, Drugs and Natural Products ISBN: 9781003089162
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe9a6d66145899093546592f06d80d8
https://hdl.handle.net/2318/1886240
https://hdl.handle.net/2318/1886240
Autor:
Margherita Miele, Vittorio Pace
Publikováno v:
Australian Journal of Chemistry. 74:623-625
Autor:
Raffaele Senatore, Wolfgang Holzer, Vittorio Pace, Karen de la Vega-Hernández, Margherita Miele, Ernst Urban
Publikováno v:
Organic & Biomolecular Chemistry. 17:1970-1978
Thioformamides are easily prepared - under full chemocontrol - through the partial reduction of isothiocyanates with the in situ generated Schwartz reagent. The high electrophilicity of the starting materials enables the straightforward addition of t
Autor:
Laura, Ielo, Margherita, Miele, Veronica, Pillari, Raffaele, Senatore, Salvatore, Mirabile, Rosaria, Gitto, Wolfgang, Holzer, Andrés R, Alcántara, Vittorio, Pace
Publikováno v:
Organicbiomolecular chemistry. 19(9)
The intrinsic degradative α-elimination of Li carbenoids somehow complicates their use in synthesis as C1-synthons. Nevertheless, we herein report how boosting such an α-elimination is a straightforward strategy for accomplishing controlled ring-op