We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer indolisation to synthesize indoles and indolines taking advantage of oxalic acid and dimethylurea. The solvent-free procedure shows versatility and wide scope; it applies to a broad range of arylhydrazines and carbonyl compounds, leading to variously decorated indoles and indolenines. Upon suitable modification, the methodology can also allow preparing compounds of pharmaceutical interest
In a new version of the Fischer indole synthesis, primary and secondary alcohols have been catalytic...
Indoles represent one of the most important heterocyclic rings which provide privileged scaffolds fo...
Indole Compounds have been prepared With good yields using Fischer syntheses in three different meth...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
International audienceWe developed an environmentally friendly mechanochemical protocol to induce an...
A new one-pot version of the titled reaction involves heating a mixture of a carbonyl compound, a ph...
Automated, miniaturized and accelerated synthesis for efficient property optimization is a formidabl...
One of the oldest and most useful reactions in organic chemistry is the Fischer indole synthesis (FI...
Functionalized indoles are synthezised under mild conditions in a tartaric acid-dimethylurea melt. T...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
The indoline skeleton is an ubiquitous scaffold found in a range of biologically active alkaloid and...
A simple and useful synthetic route to aza-polyquinane derivatives involving Fischer indolization un...
Methyl indolenines (4a-c) and(5a-c) were prepared in high yield by a Fischer indole synthesis reacti...
Functionalized indoles are synthezised under mild conditions in a tartaric acid–dimethylurea melt. T...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
In a new version of the Fischer indole synthesis, primary and secondary alcohols have been catalytic...
Indoles represent one of the most important heterocyclic rings which provide privileged scaffolds fo...
Indole Compounds have been prepared With good yields using Fischer syntheses in three different meth...
We developed an environmentally friendly mechanochemical protocol to induce an effective Fischer ind...
International audienceWe developed an environmentally friendly mechanochemical protocol to induce an...
A new one-pot version of the titled reaction involves heating a mixture of a carbonyl compound, a ph...
Automated, miniaturized and accelerated synthesis for efficient property optimization is a formidabl...
One of the oldest and most useful reactions in organic chemistry is the Fischer indole synthesis (FI...
Functionalized indoles are synthezised under mild conditions in a tartaric acid-dimethylurea melt. T...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
The indoline skeleton is an ubiquitous scaffold found in a range of biologically active alkaloid and...
A simple and useful synthetic route to aza-polyquinane derivatives involving Fischer indolization un...
Methyl indolenines (4a-c) and(5a-c) were prepared in high yield by a Fischer indole synthesis reacti...
Functionalized indoles are synthezised under mild conditions in a tartaric acid–dimethylurea melt. T...
The most preferred heterocyclic indole core was de novo assembled by an innovative 2-step reaction f...
In a new version of the Fischer indole synthesis, primary and secondary alcohols have been catalytic...
Indoles represent one of the most important heterocyclic rings which provide privileged scaffolds fo...
Indole Compounds have been prepared With good yields using Fischer syntheses in three different meth...