Zobrazeno 1 - 10
of 53
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6d4b3907060508bcfb3e02f5a8f85dd
https://pubmed.ncbi.nlm.nih.gov/31009560
https://pubmed.ncbi.nlm.nih.gov/31009560
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d7b68fc42189f94b8e8d1dd10a560a1
https://doi.org/10.1002/ejoc.201600310
https://doi.org/10.1002/ejoc.201600310
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::edd093d74cbaba8ead1e17d723ecf9c2
https://pubmed.ncbi.nlm.nih.gov/30417649
https://pubmed.ncbi.nlm.nih.gov/30417649
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0bbd28f7010db737c90b14bd2a89e2d
https://doi.org/10.1002/ejoc.201403058
https://doi.org/10.1002/ejoc.201403058
Publikováno v:
Letters in Organic Chemistry. 11:633-638
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50983640b81ad4bfbee92efd80e6a828
https://doi.org/10.2174/1570178611666140806010715
https://doi.org/10.2174/1570178611666140806010715
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3878b0057837079788aed1c96087bbb3
https://doi.org/10.1002/ejoc.201301700
https://doi.org/10.1002/ejoc.201301700
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b18de65afa2c05ca8e813badec874e1
https://doi.org/10.1002/chin.201635197
https://doi.org/10.1002/chin.201635197
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbebf38c7b0e2fbda64b731499849a03
https://doi.org/10.1002/cctc.201200122
https://doi.org/10.1002/cctc.201200122