The development of original strategies for the preparation of indole derivatives is a major goal in drug design. Herein, we report the first straight access to indoles from anilines and ethylene glycol by heterogeneous catalysis, based on an acceptorless dehydrogenative condensation, under noninert conditions. In order to achieve high selectivity, a combination of Pt/Al<sub>2</sub>O<sub>3</sub> and ZnO have been found to slowly dehydrogenate ethylene glycol generating, after condensation with the amine and tautomeric equilibrium, the corresponding pyrrole-ring unsubstituted indoles
This thesis explores the use of activated 3-substituted-4,6-dimethoxyindoles in the preparation of n...
A two-stage “tandem strategy” for the synthesis of indoles with a high level of substitution on the ...
Given the importance of heterocycle indole derivatives, much effort has been directed toward the dev...
The cross-dehydrogenative coupling (CDC) reaction is an efficient strategy for indole synthesis. How...
An efficient and metal-free method for the direct C–N coupling of indoles with azoles to produce 2-(...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
The prevalence of indoles in bioactive molecules1 has prompted the development of many useful method...
Indoles represent one of the most important heterocyclic rings which provide privileged scaffolds fo...
For the first time, ruthenium pincer complexes such as Ru-MACHO-BH were successfully used as catalys...
Easy does it: The unique properties of benziodoxolone alkynyl periodinane 1 and gold catalysts have ...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
Nitrogen containing heterocyclic compounds such as indoles, carbazoles, quinolines, β-carbolines, in...
A practical, robust and chemoselective approach toward the synthesis of pyrrolo[2,3-b]indoles via di...
This thesis explores the use of activated 3-substituted-4,6-dimethoxyindoles in the preparation of n...
A two-stage “tandem strategy” for the synthesis of indoles with a high level of substitution on the ...
Given the importance of heterocycle indole derivatives, much effort has been directed toward the dev...
The cross-dehydrogenative coupling (CDC) reaction is an efficient strategy for indole synthesis. How...
An efficient and metal-free method for the direct C–N coupling of indoles with azoles to produce 2-(...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
The prevalence of indoles in bioactive molecules1 has prompted the development of many useful method...
Indoles represent one of the most important heterocyclic rings which provide privileged scaffolds fo...
For the first time, ruthenium pincer complexes such as Ru-MACHO-BH were successfully used as catalys...
Easy does it: The unique properties of benziodoxolone alkynyl periodinane 1 and gold catalysts have ...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
Nitrogen containing heterocyclic compounds such as indoles, carbazoles, quinolines, β-carbolines, in...
A practical, robust and chemoselective approach toward the synthesis of pyrrolo[2,3-b]indoles via di...
This thesis explores the use of activated 3-substituted-4,6-dimethoxyindoles in the preparation of n...
A two-stage “tandem strategy” for the synthesis of indoles with a high level of substitution on the ...
Given the importance of heterocycle indole derivatives, much effort has been directed toward the dev...