Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Stefano Grilli"'
Autor:
Dennis Weber, Stefano Grilli
Although still under development, Pillar 2 of the OECD Global Anti-Base Erosion Model Rules is already posing significant challenges for taxation authorities worldwide. Intended to establish a floor in the possibilities for countries to compete for c
Autor:
Alessandro, Cerveri, Olalla Nieto, Faza, Carlos Silva, López, Stefano, Grilli, Magda, Monari, Marco, Bandini
Publikováno v:
The Journal of organic chemistry. 84(10)
The stereoselective phosphine-catalyzed (( pMeOC
Publikováno v:
European Journal of Organic Chemistry. 2016:3143-3156
The octa-1,7-diene-4,5-diamine skeleton is usually prepared by the addition of allylic organometallic reagents to glyoxal diimines. The relative and absolute configurations of the C4 and C5 stereocenters are dependent on the nature of the (chiral) ni
Publikováno v:
Organic letters. 20(23)
A new catalytic methodology for the direct dearomatization of substituted 2-naphthols via intermolecular condensation with allenamides is presented. PPh
A new catalytic methodology for the direct dearomatization of substituted 2-naphthols via intermolecular condensation with allenamides is presented. PPh3AuTFA (5 mol %) promotes the formal allylating dearomative protocol under mild conditions, large
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84162a6fcd8bf4f93ce7744df444c0e5
http://hdl.handle.net/11585/655350
http://hdl.handle.net/11585/655350
Publikováno v:
European Journal of Organic Chemistry. 2014:8021-8025
The synthesis of optically pure N,N′-di(tert-butoxycarbonyl)-trans-cyclohex-4-ene-1,2-diamine was accomplished from the diimine, which was obtained by condensation of glyoxal and (R)-1-(4-methoxyphenyl)ethanamine. The synthetic sequence involved th
Publikováno v:
Letters in Organic Chemistry. 11:633-638
Publikováno v:
European Journal of Organic Chemistry. 2014:1907-1914
The highly diastereoselective anti-dioxylation of (1R,2R)-1,2-bis[(1S)-phenylethylamino]cyclohexene was accomplished through epoxidation of the double bond with m-chloroperbenzoic acid (mCPBA) in the presence of a sulfonic or trihaloacetic acid and r
Publikováno v:
ChemInform. 47
The octa-1,7-diene-4,5-diamine skeleton is usually prepared by the addition of allylic organometallic reagents to glyoxal diimines. The relative and absolute configurations of the C4 and C5 stereocenters are dependent on the nature of the (chiral) ni
Autor:
Montse Guiteras Capdevila, Pier Giorgio Cozzi, Enrico Emer, Stefano Grilli, Diego Petruzziello, Andrea Gualandi
Publikováno v:
ChemCatChem; Vol 4
We have described the first organocatalytic stereoselective formylation of ketones accomplished by the use of N-methybenzothiazolylium iodide. The benzothiazolium salt, generally used as a masked formyl group or as precursor of carbenes,[31] is quite