Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mihaela Calancea"'
Publikováno v:
European Journal of Organic Chemistry. 2008:5687-5691
The 11-amino-azaelliptitoxin analog (11R,11aS,5R)-15 has been prepared stereoselectively in eight steps and 24 % overall yield from commercially available (S)-glycidol (7) via the original enantiopure chiral α-amino aldehyde 9, used as chiral precur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::448d1f19f66565057da70692e97e1e85
https://doi.org/10.1002/ejoc.200800880
https://doi.org/10.1002/ejoc.200800880
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2009, 2009 (19), pp.3134-3137. ⟨10.1002/ejoc.200900253⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2009, 2009 (19), pp.3134-3137. ⟨10.1002/ejoc.200900253⟩
(±)-Cyclocolorenone (2), an aromadendrane, was prepared stereoselectively in seven steps in 10.8–12.5 % overall yield from the commercially available tropylium cation via key intermediate 6, which was used as a general and efficient precursor to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505561641ed664c1d551bfffadf25f86
https://hal.archives-ouvertes.fr/hal-01659026
https://hal.archives-ouvertes.fr/hal-01659026
