Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Diego Savoia"'
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:
The Journal of organic chemistry. 62(12)
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:
Synthesis. :285-292
3,6-Disubstituted 4,5-di[(S)-1-phenylethylamino]-1,7-octadienes with different configurations at the carbon stereocenters were protected as dihydrochlorides or cyclic phosphorous diamides and then converted into (1R,2R)-3,6-disubstituted 1,2-diaminoc
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:
Diego Savoia, Andrea Gualandi
Publikováno v:
ChemInform. 47
Chiral, either racemic or optically pure, substituted cyclohexanes, piperidines, tetrahydrofurans and pyrrolidines can be prepared by the diastereoselective hydrogenation/reduction of the corresponding aromatic and heteroaromatic precursors, exploiti
Autor:
Diego Savoia, Andrea Gualandi
Chiral, either racemic or optically pure, substituted cyclohexanes, piperidines, tetrahydrofurans and pyrrolidines can be prepared by the diastereoselective hydrogenation/reduction of the corresponding aromatic and heteroaromatic precursors, exploiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cffb1db11da9424852c5e679e77d857d
http://hdl.handle.net/11585/537292
http://hdl.handle.net/11585/537292
Publikováno v:
Synthesis. 2011:909-918
The reactions of 1-(2-haloethyl)pyrrole-2-carbaldehydes with (1S)-1-phenylglycinol or (1S)-valinol gave the corresponding fused tricyclic oxazolidines as single diastereomers from which 1,2-disubstituted 1,2,3,4-tetrahydropyrrole[1,2-a]pyrazines were