Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtrer
Plus de filtres










Base de données
Gamme d'année
1.
Chem Pharm Bull (Tokyo) ; 72(6): 566-569, 2024.
Article de Anglais | MEDLINE | ID: mdl-38897954

RÉSUMÉ

Dihydrobenzofuran is an important skeleton for bioactive compounds and natural products. Hydroquinones can be easily modified into substituted hydroquinones, which effectively undergo oxidation to produce the corresponding benzoquinone derivatives. Benzoquinones are reactive electrophiles that are frequently utilized in coupling with olefins to dihydrobenzofurans. Herein, we report the one-pot oxidative coupling of hydroquinones bearing an electron-withdrawing group at the C2 position with olefins to dihydrobenzofurans in the presence of the Lewis acidic FeCl3 and 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) oxidant. Furthermore, this method was applied to the oxidative coupling of N-electron-withdrawing group-substituted 4-aminophenol.


Sujet(s)
Alcènes , Benzofuranes , Hydroquinones , Hydroquinones/composition chimique , Hydroquinones/synthèse chimique , Benzofuranes/composition chimique , Benzofuranes/synthèse chimique , Alcènes/composition chimique , Structure moléculaire , Couplage oxydatif , Composés du fer III/composition chimique , Oxydoréduction , Chlorures/composition chimique , Benzoquinones/composition chimique , Benzoquinones/synthèse chimique
2.
ChemMedChem ; 19(16): e202400201, 2024 Aug 19.
Article de Anglais | MEDLINE | ID: mdl-38740557

RÉSUMÉ

Deuterated drugs (heavy drugs) have recently been spotlighted as a new modality for small-molecule drugs because the pharmacokinetics of pharmaceutical drugs can be enhanced by replacing C-H bonds with more stable C-D bonds at metabolic positions. Therefore, deuteration methods for drug candidates are a hot topic in medicinal chemistry. Among them, the H/D exchange reaction (direct transformation of C-H bonds to C-D bonds) is a useful and straightforward method for creating novel deuterated target molecules, and over 20 reviews on the synthetic methods related to H/D exchange reactions have been published in recent years. Although various deuterated drug candidates undergo clinical trials, approved deuterated drugs possess CD3 groups in the same molecule. However, less diversification, except for the CD3 group, is a problem for future medicinal chemistry. Recently, we developed various deuterated alkyl (dn-alkyl) sulfonium salts based on the H/D exchange reaction of the corresponding hydrogen form using D2O as an inexpensive deuterium source to introduce CD3, CH3CD2, and ArCH2CD2 groups into drug candidates. This concept summarises recent reviews related to H/D exchange reactions and novel reagents that introduce the CD3 group, and our newly developed electrophilic dn-alkyl reagents are discussed.


Sujet(s)
Deutérium , Découverte de médicament , Deutérium/composition chimique , Composés de sulfonium/composition chimique , Sels/composition chimique , Sels/synthèse chimique , Structure moléculaire , Indicateurs et réactifs/composition chimique , Humains , Mesure d'échange de deutérium
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE