690629-90-4Relevant academic research and scientific papers
(±)-cis-(6-Ethyl-tetrahydropyran-2-yl)-formic acid: A novel substance with antinociceptive properties
Miranda,Marinho, Bruno G.,Leit?o, Suzana G.,Matheus, Maria Eline,Fernandes, Patrícia D.,Vasconcellos
, p. 1573 - 1575 (2004)
We described in this paper the first synthesis to the (±) cis (6-ethyl-tetrahydropyran-2-yl) formic acid (1) using the very efficient Prins cyclization reaction as strategy to construction of its tetrahydropyran skeleton. This new compound presented a significant antinociceptive property by the tail-flick model.
Design, Prins-cyclization reaction promoting diastereoselective synthesis of 10 new tetrahydropyran derivatives and in vivo antinociceptive evaluations
Capim, Saulo L.,Carneiro, Paulo H.P.,Castro, Paloma C.,Barros, Maithê R.M.,Marinho, Bruno G.,Vasconcellos, Mário L.A.A.
, p. 1 - 11 (2012)
We described in this article the very efficient 2,6-cis ou 2,4,6-cis diastereoselective synthesis (2 or 3 steps, 62-65% global yields) from Prins-cyclization reaction as synthetic key-step to tetrahydropyran rings construction of 10 new congeners compounds (3-12) designed from Naproxen structure. These tetrahydropyran derivatives were in vivo bioevaluated on antinociceptive effect in the acetic acid-induced abdominal writhing test, the tail-flick test, the rota-rod performance and open field tests. All new compounds showed greater antinociceptive activity compared to compound 1a, an analgesic tetrahydropyran derivative previously described by us. We can detach the high activity of tetrahydropyran derivative 10 which presented 87.5% inhibition (14% inhibition was presented by 1a) in the acetic acid-induced abdominal writhing test. Besides that the tail-flick tests indicate compounds 7 and 10 as the most actives. All these new compounds showed no toxicity in mice in all biologically studied models.
First enantioselective synthesis of (-)-(2s,6s)-(6-ethyltetrahydropyran-2- yl)formic acid
Miranda, Leandro S. M.,Meireles, Bruno A.,Costa, Jer?nimo S.,Pereira, Vera L. P.,Vasconcellos, Mário L. A. A.
, p. 869 - 871 (2005)
We describe in this letter the first enantioselective synthesis of (-)-(2S,6S)-(6-ethyltetrahydropyran-2-yl)formic acid (2) in five steps (30% overall yield, 87% ee), from the commercial chiral template (R)-2,3- isopropylideneglyceraldehyde (4). The two stereogenic centers in 2 were controlled by diastereoselective Barbier allylation of 4 in aqueous media and an efficient Prins cyclization reaction between 5 with propanal.
