Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Serena Monticelli"'
Autor:
Serena Monticelli, Alex Talbot, Philipp Gotico, Fabien Caillé, Olivier Loreau, Antonio Del Vecchio, Augustin Malandain, Antoine Sallustrau, Winfried Leibl, Ally Aukauloo, Frédéric Taran, Zakaria Halime, Davide Audisio
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Harvesting sunlight to drive carbon dioxide (CO2) valorisation represents an ideal concept to support a sustainable and carbon-neutral economy. While the photochemical reduction of CO2 to carbon monoxide (CO) has emerged as a hot research to
Externí odkaz:
https://doaj.org/article/92751b4c62044d338dedd1228c161d56
Publikováno v:
Advanced Synthesis & Catalysis. 361:1001-1006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946b8a729e9ad1a03c229ab9c4aa6df2
https://doi.org/10.1002/adsc.201801614
https://doi.org/10.1002/adsc.201801614
Autor:
Ugo Azzena, Massimo Carraro, Luisa Pisano, Vittorio Pace, Serena Monticelli, Roberta Bartolotta
Publikováno v:
Chemsuschem
Solvents represent one of the major contributions to the environmental impact of fine‐chemical synthesis. As a result, the use of environmentally friendly solvents in widely employed reactions is a challenge of vast real interest in contemporary or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbef3bacab0144694d266104bca53f02
http://europepmc.org/articles/PMC6391966
http://europepmc.org/articles/PMC6391966
Autor:
Giovanna Parisi, Wolfgang Holzer, Giuseppe Romanazzi, Serena Monticelli, Marco Colella, Leonardo Degennaro, Thierry Langer, Vittorio Pace, Renzo Luisi
Publikováno v:
Journal of the American Chemical Society. 139:13648-13651
The first direct and straightforward nucleophilic fluoromethylation of organic compounds is reported. The tactic employs a “fleeting” lithium fluorocarbenoid (LiCH2F) generated from commercially available fluoroiodomethane. Precise reaction condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e27019ce2f7ae9ef479a69bf0b443bde
https://doi.org/10.1021/jacs.7b07891
https://doi.org/10.1021/jacs.7b07891
Autor:
Thierry Langer, Wolfgang Holzer, Arianna Tota, Veronica Pillari, Leonardo Degennaro, Renzo Luisi, Marco Colella, Serena Monticelli, Vittorio Pace
Publikováno v:
Organic letters. 21(2)
An expeditious, high-yielding synthesis of rare α-fluoroepoxides and α-fluoroaziridines through the addition of the unkown fluoroiodomethyllithium (LiCHIF)—formed via deprotonation the commercially available fluoroiodomethane with a lithium amide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ee576d508fc5a6c6004b6e652d50c14
https://pubmed.ncbi.nlm.nih.gov/30600682
https://pubmed.ncbi.nlm.nih.gov/30600682
The acylation of α-substituted carbanion-type reagents (MCR1R2X; X = halogen, OR, SR, NR3R4, SeR, etc.) with Weinreb amides constitutes a highly versatile and flexible approach for accessing α-functionalized ketones. In this short review we will pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28e4ab3dba488b278ca8f8ce5b702e92
http://hdl.handle.net/2318/1835430
http://hdl.handle.net/2318/1835430
Autor:
Christoph Schwarzer, Ernst Urban, Vittorio Pace, Steffen Hering, Thierry Langer, Stefan Boehm, Serena Monticelli, Thomas Seidel, Sophia Khom, Isabella Salzer, Marco Stadler, Wolfgang Holzer, Denise Luger
Subunit-selective modulation of γ-aminobutyric acid type A receptors (GABAAR) is considered to exert fewer side effects compared to unselective clinically used drugs. Here, the β2/3 subunit-selective GABAAR modulators valerenic acid (VA) and lorecl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::427fad6c4d3ff843ff98b259c45a5c63
http://hdl.handle.net/2318/1842712
http://hdl.handle.net/2318/1842712
Publikováno v:
Organic & Biomolecular Chemistry. 14:7848-7854
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reagent) to isocyanates and isothiocyanates constitutes a versatile, direct and high yielding approach to the synthesis of functionalized (thio)amide deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61bfc02d17b58dd4f101afe6037fa317
https://doi.org/10.1039/c6ob00766j
https://doi.org/10.1039/c6ob00766j
Autor:
Alexander Roller, Thierry Langer, Serena Monticelli, Wolfgang Holzer, Vittorio Pace, Berit Olofsson
Publikováno v:
Chemsuschem
The well‐established Hoppe–Beak chemistry, which involves enantioselective generation of organolithium compounds in the presence of (−)‐sparteine, was revisited and applied to unprecedented acylations with Weinreb amides to access highly enan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef96be6f39a53b9ec69d82143a6f41e
https://pubmed.ncbi.nlm.nih.gov/30614208
https://pubmed.ncbi.nlm.nih.gov/30614208
Autor:
Serena, Monticelli, Giovanna, Parisi, Marta, Rui, Karen, de la Vega-Hernández, Irene, Murgia, Raffaele, Senatore, Wolfgang, Holzer, Ernst, Urban, Thierry, Langer, Vittorio, Pace
Publikováno v:
Natural product communications. 11(11)
Formylation reactions are fundamental operations in synthetic chemistry allowing the incorporation into a given structure formyl groups amenable to further deiivatization. Conceptually, the introduction of such groups through the reaction between an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd97fadcd4fbcd1da85a1c81976ead9b
https://pubmed.ncbi.nlm.nih.gov/30475518
https://pubmed.ncbi.nlm.nih.gov/30475518