Benzofurans are important synthetic building blocks present in a high number of biologically active natural products, pursuing several medicinal properties. In this context, there is an increasing interest in developing efficient syntheses for this class of compounds. Accordingly, we present in this work our preliminary results involving the iodocyclization reaction of 2-iodo-6-alkynylanisoles, employing molecular iodine under mild conditions, leading to the formation of highly functionalized benzofurans, potential precursors of pharmaceuticals and functional materials.</em
Benzofuran itself is an oily chemical compound, extracted from coal tar, which is converted into a s...
In this thesis, the synthesis, characterization and application, in a series of model organic synthe...
An efficient method to effect C–O cyclization was developed via the C–H functionalization of chromon...
Research on natural products containing benzofuran has remarkably increased during the past few deca...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Herein we report on the retrosynthetic production of 3-iodo-2-(2-methoxyphenyl)-benzofuran in 4 synt...
The generation of indolines and benzofurans from the combination of Suzuki–Miyaura coupling reaction...
A new methodology for the synthesis of indole and benzofuran derivatives has been devised. The start...
This thesis describes the synthesis of bioactive benzofuran compounds using the halogen-metal exchan...
A new and convenient metal-free cyclization of ortho-hydroxystilbenes into 2-arylbenzofurans and 2-a...
Heterocyclic compounds are commonly found in the core structures of several pharmaceuticals, natural...
A general method to synthesize conjugated molecules with a benzofulvene core is reported. Up to four...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
This report describes the recent applications of hypervalent iodine reagents in the total synthesis ...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
Benzofuran itself is an oily chemical compound, extracted from coal tar, which is converted into a s...
In this thesis, the synthesis, characterization and application, in a series of model organic synthe...
An efficient method to effect C–O cyclization was developed via the C–H functionalization of chromon...
Research on natural products containing benzofuran has remarkably increased during the past few deca...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Herein we report on the retrosynthetic production of 3-iodo-2-(2-methoxyphenyl)-benzofuran in 4 synt...
The generation of indolines and benzofurans from the combination of Suzuki–Miyaura coupling reaction...
A new methodology for the synthesis of indole and benzofuran derivatives has been devised. The start...
This thesis describes the synthesis of bioactive benzofuran compounds using the halogen-metal exchan...
A new and convenient metal-free cyclization of ortho-hydroxystilbenes into 2-arylbenzofurans and 2-a...
Heterocyclic compounds are commonly found in the core structures of several pharmaceuticals, natural...
A general method to synthesize conjugated molecules with a benzofulvene core is reported. Up to four...
Quinolones are important heterocyclic compounds in medicine and materials for DSSC or OLED. This stu...
This report describes the recent applications of hypervalent iodine reagents in the total synthesis ...
This thesis concerns the development of metal-free reactions to obtain carbon-heteroatom and carbon-...
Benzofuran itself is an oily chemical compound, extracted from coal tar, which is converted into a s...
In this thesis, the synthesis, characterization and application, in a series of model organic synthe...
An efficient method to effect C–O cyclization was developed via the C–H functionalization of chromon...