C07C41/32

Abietanes and methods of making and using the same

In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein is versatile polyene cyclization strategy that exploits conjugated -ionyl derivatives. Photomediated disruption of the extended -system within these chromophores unveils a contra-thermodynamic polyene that engages in a Heck-type cyclization to afford [4.4.1]-propellanes. The connectivity of overbred polycycles generated from this process is controlled by the position of the requisite C-Halide bond. Thus, compared to conventional biomimetic polyene cyclization, this approach allows for complete control of regiochemistry and facilitates incorporation of both electron-rich and electron-deficient (hetero)aryl groups. This strategy was successfully applied to the total synthesis of abietanes such as, for example, taxodione and salviasperanol, two isomeric abietane-type diterpenes that previously could not be prepared along the same synthetic pathway.

Process for the synthesis of agomelatine

Process for the industrial synthesis of the compound of formula (I): ##STR00001##

Process for the synthesis of agomelatine

Process for the industrial synthesis of the compound of formula (I): ##STR00001##

TRIBENZOTRIQUINACENE WITH AXIAL ARYL GROUP AND METHOD FOR PREPARING THE SAME

The present disclosure discloses tribenzotriquinacene with an axial aryl group and a method for preparing the same. The triphenyltripentacene has a structure shown in formula (1):

##STR00001##

R.sub.1 and R.sub.2 are independently hydrogen, a C1-C12 alkyl group, a C1-C12 alkoxy group, a C1-C12 fluoroalkyl group, a C1-C12 fluorine-containing alkoxy group, a C1-C12 ester group, a halogen group, a nitro group, an amine group, a cyano group, or a hydroxy group.

TRIBENZOTRIQUINACENE WITH AXIAL ARYL GROUP AND METHOD FOR PREPARING THE SAME

The present disclosure discloses tribenzotriquinacene with an axial aryl group and a method for preparing the same. The triphenyltripentacene has a structure shown in formula (1):

##STR00001##

R.sub.1 and R.sub.2 are independently hydrogen, a C1-C12 alkyl group, a C1-C12 alkoxy group, a C1-C12 fluoroalkyl group, a C1-C12 fluorine-containing alkoxy group, a C1-C12 ester group, a halogen group, a nitro group, an amine group, a cyano group, or a hydroxy group.