Add to ORKG1291-1295Silica sulfuric acid has been found to be an efficient and reusable catalyst for chemoselective dithioacetalization of aldehydes over ketones, in excellent yields
Thiosilanes react efficiently with simple aldehydes and ketones when catalyzed with ZnI_2 to produce...
Lithium tetrafluoroborate is found to be an efficient catalyst for the chemoselective protection of ...
Present methods to synthesize 1,3-dithiane molecules require either harsh reaction conditions or hig...
A new procedure for the protection of aldehydes and ketones as thioacetals promoted by catalytic amo...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
<p>An efficient heterogeneous method for the synthesis of diarylacetic acids was developed utilizing...
1,1-Diacetates are prepared in excellent yields from aldehydes and acetic anhydride under solvent-fr...
Aromatic aldehydes undergo crossed-aldol condensation with ketones in the presence of silica sulfuri...
A highly efficient, green and expeditious solvent-free method is described for the chemoselective co...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
1054-1056The reac tion of aldehyde with acetic anhydride catalyzed by silica sulfate results in 1,1-...
Neat chlorosulfonic acid reacts with silica gel to give silica sulfuric acid in which sulfuric acid ...
A simple and efficient thiol-mediated addition of ketones to aromatic and aliphatic aldehydes is rep...
Thiosilanes react efficiently with simple aldehydes and ketones when catalyzed with ZnI_2 to produce...
Lithium tetrafluoroborate is found to be an efficient catalyst for the chemoselective protection of ...
Present methods to synthesize 1,3-dithiane molecules require either harsh reaction conditions or hig...
A new procedure for the protection of aldehydes and ketones as thioacetals promoted by catalytic amo...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
Aldehydes were cleanly and selectively converted to the corresponding dithioacetals almost quantitat...
<p>An efficient heterogeneous method for the synthesis of diarylacetic acids was developed utilizing...
1,1-Diacetates are prepared in excellent yields from aldehydes and acetic anhydride under solvent-fr...
Aromatic aldehydes undergo crossed-aldol condensation with ketones in the presence of silica sulfuri...
A highly efficient, green and expeditious solvent-free method is described for the chemoselective co...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
1054-1056The reac tion of aldehyde with acetic anhydride catalyzed by silica sulfate results in 1,1-...
Neat chlorosulfonic acid reacts with silica gel to give silica sulfuric acid in which sulfuric acid ...
A simple and efficient thiol-mediated addition of ketones to aromatic and aliphatic aldehydes is rep...
Thiosilanes react efficiently with simple aldehydes and ketones when catalyzed with ZnI_2 to produce...
Lithium tetrafluoroborate is found to be an efficient catalyst for the chemoselective protection of ...
Present methods to synthesize 1,3-dithiane molecules require either harsh reaction conditions or hig...