Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Giovanni Papandrea"'
Autor:
Fabio Ponticelli, Giovanni Papandrea
Publikováno v:
Synthetic Communications. 38:858-865
This article describes a new route to peptidosulfonamide. Our study shows how sulfinamides were first obtained via nucleophilic cleavage of 3,6‐dihydrothiazine‐1‐oxide system and how the products can be subjected to oxidation with m‐chloroper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3850ab5ab5ab9b4efb34efcf479d18b3
https://doi.org/10.1080/00397910701845340
https://doi.org/10.1080/00397910701845340
Publikováno v:
Tetrahedron Letters. 47:1749-1752
A new cyclopentene GABA analogue was synthesized as a conformationally rigid analogue of the epilepsy drug vigabatrin. N -Sulfinyl dienophile Diels–Alder methodology, followed by alkaline hydrolysis of the corresponding dihydrothiazine oxide, oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3094f5f8119a105a50730f80f4eec376
https://doi.org/10.1016/j.tetlet.2006.01.040
https://doi.org/10.1016/j.tetlet.2006.01.040
Autor:
Fabio Ponticelli, Giovanni Papandrea
Publikováno v:
ChemInform. 39
This article describes a new route to peptidosulfonamide. Our study shows how sulfinamides were first obtained via nucleophilic cleavage of 3,6‐dihydrothiazine‐1‐oxide system and how the products can be subjected to oxidation with m‐chloroper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb84ea4157aa6e4db65bb220e0867732
https://doi.org/10.1002/chin.200832190
https://doi.org/10.1002/chin.200832190