Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Margherita Pirola"'
Publikováno v:
Molecules, Vol 24, Iss 12, p 2260 (2019)
A stereoselective synthetic strategy for the preparation of trifluoromethylamine mimics of retro-thiorphan, involving a diastereoselective, metal-free catalytic step, has been studied in batch and afforded the target molecule in good yields and high
Externí odkaz:
https://doaj.org/article/8822a27dd1514cc399e062b9358cfac2
Metal-Free Alpha Trifluoromethylselenolation of Carbonyl Derivatives under Batch and Flow Conditions
Publikováno v:
Molecules, Vol 24, Iss 4, p 726 (2019)
Trifluoromethylselenolated carbonyl compounds represent an emerging class with potential applications in several fields; however, a widespread use of such compound is hampered by the very limited number of strategies for their preparation. In this st
Externí odkaz:
https://doaj.org/article/6ad8758dd02c41259dc0c7ce3e13f88a
Publikováno v:
European Journal of Organic Chemistry. 2020:4641-4651
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffc32a56d2c6ad8ddf48710448af4976
https://doi.org/10.1002/ejoc.202000080
https://doi.org/10.1002/ejoc.202000080
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(40)
A metal-free, mild and chemodivergent transformation involving nitroalkanes has been developed. Under optimized reaction conditions, in the presence of trichlorosilane and a tertiary amine, aliphatic nitroalkanes were selectively converted into amine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdc31c8fbb34a7bff2ac5d410bf5135a
https://pubmed.ncbi.nlm.nih.gov/34021644
https://pubmed.ncbi.nlm.nih.gov/34021644
Autor:
Margherita Pirola, Alessandra Puglisi, Maurizio Benaglia, Laura Raimondi, Maria Elena Compostella
Publikováno v:
Synthesis. 50:1430-1438
The enantioselective organocatalytic reduction of aryl-substituted nitroenamines was successfully performed under continuous-flow conditions. After a preliminary screening with a 10-μL microreactor, to establish the best reaction conditions, the red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32b97a425bf5d30a33092d15ddecbbdc
https://doi.org/10.1055/s-0036-1591911
https://doi.org/10.1055/s-0036-1591911
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
The diastereoselective, trichlorosilane-mediate reduction of imines, bearing different and removable chiral auxiliaries, in combination either with achiral bases or catalytic amounts of chiral Lewis bases, was investigated to afford immediate precurs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ae87946df2ff060c0fffe3920ea942
https://doi.org/10.1016/j.bmc.2017.01.023
https://doi.org/10.1016/j.bmc.2017.01.023