نتایج جستجو برای: octahydroxanthene
تعداد نتایج: 33 فیلتر نتایج به سال:
An efficient one-pot condensation for the synthesis of 1,8-dioxo-octahydroxanthene is achieved through a condensation of aryl aldehydes and 5,5-dimethyl-1,3-cyclohexandione in the presence of NBS. This method enjoys several advantages such as low cost, simple work up procedure and safe reaction condition. In addition, water was chosen as a green solvent.
an efficient one-pot condensation for the synthesis of 1,8-dioxo-octahydroxanthene is achieved through a condensation of aryl aldehydes and 5,5-dimethyl-1,3-cyclohexandione in the presence of nbs. this method enjoys several advantages such as low cost, simple work up procedure and safe reaction condition. in addition, water was chosen as a green solvent.
1,3-Dibromo-5,5-dimethylhydantoin (DBH) and benzyltriphenylphosphoniumtribromide (BTPTB) were used as efficient catalysts for the promotion of the synthesis of 1,8-dioxo-octahydroxanthene derivatives (DOXOs) via a one-pot three component condensation of aldehydes and cyclic 1,3-dicarbonyl compounds in the absence of solvent.
1, 8-Dioxo-octahydroxanthene derivatives have efficiently been synthesized from dimedone and aromatic aldehydes using [Fe(III)(salen)Cl] complex as an efficient and homogeneous catalyst in molten tetrabutyl ammonium bromide. This methodology offers several advantages, such as good yields, short reaction times, simple procedure, and mild conditions.
A novel, simple and environmentally friendly method is reported for the preparation of 1,8-dioxo-octahydroxanthene derivatives by the reaction of dimedon with various aromatic aldehydes, using thiamine chloride as a recyclable catalyst under solvent-free conditions. This procedure has following benefits; simple workup, moderate reaction times, good yields, and completely compatible with enviro...
A novel, simple and environmentally friendly method is reported for the preparation of 1,8-dioxo-octahydroxanthene derivatives by the reaction of dimedon with various aromatic aldehydes, using thiamine chloride as a recyclable catalyst under solvent-free conditions. This procedure has following benefits; simple workup, moderate reaction times, good yields, and completely compatible with enviro...
1,3-dibromo-5,5-dimethylhydantoin (dbh) and benzyltriphenylphosphoniumtribromide (btptb) were used as efficient catalysts for the promotion of the synthesis of 1,8-dioxo-octahydroxanthene derivatives (doxos) via a one-pot three component condensation of aldehydes and cyclic 1,3-dicarbonyl compounds in the absence of solvent.
in this study, aluminosilicate mcm-41 has been found to be an efficient catalyst for reaction betweendifferent benzaldehyde derivatives and 5,5-dimethyl-1,3-cyclohexanedione to give open chain analogue of1,8-dioxo-octahydroxanthene in excellent yields. no evidence for the formation of cyclization products wasobserved. the catalyst can be used several times after recovery.
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